COMPOSITIONS AND METHODS FOR INCREASING THE EFFICIENCY OF CELL CULTURES USED FOR FOOD PRODUCTION

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of co-pending U.S. patent application Ser. No. 16/630,404, filed Jan. 10, 2020, which is the 371 National Stage application of PCT Application No. PCT/US2018/042187, filed Jul. 13, 2018, which claims the benefit of and priority to U.S. Provisional Application No. 62/532,345, filed Jul. 13, 2017, all of which are hereby incorporated by reference in their entireties for all purposes.

REFERENCE TO SEQUENCE LISTING

The instant application contains a Sequence Listing with 58 sequences, which has been submitted in XML format and is hereby incorporated herein by reference in its entirety. Said XML copy, created on Sep. 2, 2022, is named 39028-53373-Sequence-Listing.xml, and is 125 kilobytes (KB) in size.

BACKGROUND OF THE INVENTION

The mass production of cells for biomass production remains limited by several factors, thus limiting final yields. Examples of such factors include (1) accumulation of extracellular metabolic waste products such as ammonia/ammonium hydroxide, in the cell culture medium to toxic levels, (2) depletion of necessary nutrients, such as glutamine, in the cell culture medium, requiring a constant supply and supplementation of such nutrients, incurring both expense and additional manipulation of the cells, and the (3) requirement for supplemented proteins, such as growth factors, which support the productivity of a cultivation process.

Provided herein are compositions and methods that address this need.

BRIEF SUMMARY OF THE INVENTION

Provided herein are compositions and methods to make and use modified cells, for the purpose of increasing the efficiency of cell cultures, increasing the cell density of metazoan cell cultures, and for making a cultured edible product for human or non-human consumption.

In one aspect, provided herein is a method for increasing the cell density of a culture comprising metazoan cells, the method comprising: (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), and albumin; and (b) culturing the cells in a cultivation infrastructure.

In another aspect, provided herein is a method for increasing the cell density of a culture comprising metazoan cells, the method comprising: (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof; and (b) culturing the cells in a cultivation infrastructure.

In yet another aspect, provided herein is a method for increasing the cell density of a culture comprising metazoan cells, the method comprising: (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof; (b) introducing into the cells a polynucleotide sequence encoding a telomerase reverse transcriptase (TERT); and (c) culturing the cells in a cultivation infrastructure.

In one aspect provided herein is a method of decreasing the concentration of ammonia and/or ammonium hydroxide in the medium of cells in culture comprising increasing the expression of glutamine synthetase (GS) protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of ammonia (i.e. ammonium hydroxide) in the medium is decreased by at least 2.5%.

In another aspect, provided herein is a method of increasing the production of glutamine in cells comprising increasing the expression of glutamine synthetase (GS) protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of glutamine in the cells is increased by at least 2.5%.

In another aspect, provided herein, is a method of increasing the concentration of Insulin-like growth factor (IGF) in the medium of cells in culture comprising increasing the expression of IGF protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of IGF in the medium is increased by at least 2.5% or is increased to at least 0.001 ng/mL.

In another aspect, provided herein is a method of increasing the concentration of albumin in the medium of cells in culture comprising increasing the expression of albumin in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of albumin in the medium is increased at least 2.5% or is increased to at least 0.1 μg/mL.

In one aspect, provided herein is an in vitro method for producing a cultured edible product, the method comprising: (a) introducing one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof into myogenic cells; (b) optionally introducing a polynucleotide sequence encoding a telomerase reverse transcriptase (TERT) into the cells; (c) inducing myogenic differentiation of the cells expressing GS, IGF, albumin or combinations thereof and optionally TERT, wherein the differentiated cells form myocytes and multinucleated myotubes; and (d) culturing the myocytes and myotubes to generate skeletal muscle fibers, thereby producing a cultured edible product.

In another aspect, provided herein is an in vitro method for producing a cultured edible product, the method comprising: (a) overexpressing GS, IGF, albumin, or a combination thereof in a self-renewing cell line, wherein the cell line is a myogenic transcription factor-modified cell line, and wherein the cell line is of a livestock, poultry, game or aquatic animal species; (b) inducing myogenic differentiation of the cell line, wherein the differentiated cell line forms myocytes and multinucleated myotubes; and (c) culturing the myocytes and myotubes to generate skeletal muscle fibers, thereby producing a cultured edible product. In another aspect provided herein is a cultured edible product produced by the in vitro method.

In one aspect, provided herein is a method for increasing the secretion of glutamine by cells into a culture medium, the method comprising increasing the expression of a glutamine synthetase (GS) protein in the cells, wherein the cells are from livestock, poultry, game or aquatic animal species, and wherein the concentration of glutamine secreted into the culture medium is increased by at least 2.5%.

In one aspect, provided herein is a method for increasing the rate of proliferation of cells in a cultivation infrastructure, comprising: (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof; and (b) culturing the cells in a cultivation infrastructure, wherein the cells are from livestock, poultry, game or aquatic animal species.

In another aspect, provided herein is a method for decreasing death of cells in a cultivation infrastructure, comprising: (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof; and (b) culturing the cells in a cultivation infrastructure, wherein the cells are from livestock, poultry, game or aquatic animal species.

In another aspect, provided herein is a method for increasing protein production in cells in a cultivation infrastructure, comprising: (a) introducing into the cells a polynucleotide sequence encoding insulin-like growth factor (IGF); and (b) culturing the cells in a cultivation infrastructure, wherein the cells are from livestock, poultry, game or aquatic animal species.

In another aspect provided herein is a cultured edible product comprising cells having increased expression of GS, increased expression of IGF, increased expression of albumin, increased expression of telomerase reverse transcriptase (TERT), loss-of-function mutations in cyclin-dependent kinase inhibitor (CKI) proteins, increased expression of YAP, increased expression of TAZ, and/or increased expression of myogenic transcription factors.

In another aspect provided herein is a construct comprising any one of the sequences selected from Tables 1A and 1B.

In another aspect provided herein is an expression vector comprising any one of the sequences selected from Tables 1A and 1B.

In another aspect provided herein is a cell comprising an expression vector comprising any one of the sequences selected from Tables 1A and 1B. In some embodiments, the cell is from a livestock, poultry, game, or aquatic species.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a spontaneous increase in ammonia concentration in various cell culture media.

FIGS. 2A-D show morphology of wild type duck fibroblast cells following transfection with a glutamine synthetase (GS) gene. FIG. 2A shows fibroblasts transfected with vehicle-only and grown in media with supplemented glutamine. FIG. 2B shows fibroblasts transfected with mouse GS and grown in media with supplemented glutamine. FIG. 2C shows fibroblasts transfected with vehicle-only and grown in media without supplemented glutamine.

FIG. 2D shows fibroblasts transfected with a mouse GS gene and grown in media without supplemented glutamine.

FIG. 3 demonstrates quantification of ammonia levels in media following transfection of wild type duck fibroblast cells with a GS gene.

FIG. 4 shows an increase in glutamine in culture media from duck fibroblast cell cultures normalized to culture medium in which no cells were present.

FIGS. 5A-D show morphology of wild-type duck myoblast cells following transfection with GS. FIG. 5A shows myoblasts transfected with vehicle-only and grown in medium with supplemented glutamine. FIG. 5B shows myoblasts transfected with mouse GS and grown in media with supplemented glutamine. FIG. 5C shows myoblasts transfected with vehicle-only and grown in media without supplemented glutamine. FIG. 5D shows myoblasts transfected with a mouse GS gene and grown in media without supplemented glutamine.

FIG. 6 demonstrates quantification of ammonia levels in media following transfection of wild type duck myoblast cells with a GS gene.

FIG. 7 shows an increase in glutamine in in culture media from myoblast cultures normalized to culture medium in which no cells were present.

FIG. 8 shows a comparison of normalized ammonia levels between culture media from myoblast cultures and culture media from fibroblast cultures.

FIG. 9 depicts predicted extension of growth period before media reaches growth-limiting ammonia concentration.

FIGS. 10A-D show morphology of wild type duck fibroblast cells following transfection with IGF-1, mouse albumin, or human albumin genes. FIG. 10A shows fibroblasts transfected with vehicle-only. FIG. 10B shows fibroblasts transfected with a human IGF-1 gene.

FIG. 10C Fibroblasts transfected with a mouse albumin gene. FIG. 10D shows fibroblasts transfected with a human albumin gene.

FIGS. 11A-D show morphology of duck myoblasts following transfection with IGF-1, mouse albumin, or human albumin genes. FIG. 11A shows myoblasts transfected with vehicle-only. FIG. 11B shows myoblasts transfected with a human IGF-1 gene. FIG. 11C shows myoblasts transfected with a mouse albumin gene. FIG. 11D shows myoblasts transfected with human albumin gene.

FIG. 12 shows IGF-1 levels secreted in myoblast cell culture media.

DETAILED DESCRIPTION OF THE INVENTION

Provided herein are compositions and methods to make and use engineered cells, for the purpose of increasing the efficiency of cell cultures. Specifically, provided herein are exemplary methods of increasing culture density (e.g. cell density of metazoan cells in culture) and methods for producing cultured edible product. Also provided are methods of making and using cells with reduced requirements for glutamine supplementation, and reduced supplementation with certain animal-cell secreted components such as insulin-like growth factor (IGF) and albumin.

Before describing certain embodiments in detail, it is to be understood that this invention is not limited to particular compositions or biological systems, which can vary. It is also to be understood that the terminology used herein is for the purpose of describing particular illustrative embodiments only, and is not intended to be limiting. The terms used in this specification generally have their ordinary meaning in the art, within the context of this invention and in the specific context where each term is used. Certain terms are discussed below or elsewhere in the specification, to provide additional guidance to the practitioner in describing the compositions and methods of the invention and how to make and use them. The scope and meaning of any use of a term will be apparent from the specific context in which the term is used. As such, the definitions set forth herein are intended to provide illustrative guidance in ascertaining particular embodiments of the invention, without limitation to particular compositions or biological systems.

As used in the present disclosure and the appended claims, the singular forms “a,” “an” and “the” include plural references unless the content clearly dictates otherwise.

Throughout the present disclosure and the appended claims, unless the context requires otherwise, the word “comprise”, or variations such as “comprises” or “comprising”, will be understood to imply the inclusion of a stated element or group of elements but not the exclusion of any other element or group of elements.

Standard techniques may be used for recombinant DNA, oligonucleotide synthesis, and tissue culture and transduction (e.g., electroporation, transfection). Enzymatic reactions and purification techniques may be performed according to manufacturer's specifications or as commonly accomplished in the art or as described herein. These and related techniques and procedures may be generally performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present specification. Unless specific definitions are provided, the nomenclature utilized in connection with, and the laboratory procedures and techniques of, molecular biology, analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those well-known and commonly used in the art. Standard techniques may be used for recombinant technology, molecular biological, microbiological, chemical syntheses, chemical analyses, pharmaceutical preparation, production, and delivery.

Cells

Provided herein are methods for modifying cells to overexpress and/or inhibit certain gene products, for the purpose of achieving increased cell density and in some embodiments, for the purpose of providing a cultured edible product. For example, in certain aspects, cells modified as described herein may be cultivated for food production, e.g. production of cultured chicken, cultured beef, and cultured fish.

The cells used in the methods of the present disclosure can be primary cells, or cell lines. The methods provided herein are applicable to any metazoan cell in culture. In various embodiments, methods of the present disclosure may use any one of the cell populations described herein.

In some embodiments, the cells are harvested for the production of cell-based food products, such as cultured edible product from an animal (e.g. cultured poultry, cultured livestock, cultured game, cultured fish). Thus in some embodiments, the methods utilize cells with the potential to differentiate into skeletal muscle. In certain embodiments, the cells are from livestock such as domestic cattle, pigs, sheep, goats, camels, water buffalo, rabbits and the like. In certain embodiments, the cells are from poultry such as domestic chicken, turkeys, ducks, geese, pigeons and the like. In certain embodiments, the cells are from game species such as wild deer, gallinaceous fowl, waterfowl, hare and the like. In certain embodiments, the cells are from aquatic species or semi-aquatic species harvested commercially from wild fisheries or aquaculture operations, or for sport, including certain fish, crustaceans, mollusks, cephalopods, cetaceans, crocodilians, turtles, frogs and the like. In certain embodiments, the cells are from exotic, conserved or extinct animal species. In certain embodiments, the cells are from any metazoan species demonstrating the capacity for skeletal muscle tissue specification. In certain embodiments, the cells are modifiable by a genetic switch to induce rapid and efficient conversion of the cells to skeletal muscle for cultured food production (e.g. cultured poultry, cultured livestock, cultured game, and cultured fish).

In some embodiments, the cells are from Gallus gallus, Bos taurus, Sous scrofa, Meleagris gallopavo, Anas platyrynchos, Salmo solar, Thunnus thynnus, Ovis aries, Coturnix coturnix, Capra aegagrus hircus, or Homarus americanus.

In some embodiments, the cells are from any animal species intended for human or non-human dietary consumption.

In some embodiments, the cells are from livestock, poultry, game, or aquatic species. In other embodiments, the cells are from humans, primates (e.g. monkeys), rodents, including rats and mice, and companion animals such as dogs, cats, horses, and the like.

In some embodiments, the cells are self-renewing stem cell lines.

In some embodiments, the cells are satellite cells, myoblasts, myocytes, fibroblasts, induced pluripotent stem cells, hepatocytes, vascular endothelial cells, pericytes, embryonic stem cells, mesenchymal stem cells, extraembryonic cell lines, somatic cell lines, adipocytes, embryonic stem cells or chondrocytes.

In some embodiments, the cells are myogenic cells. In some embodiments, the myogenic cells are natively myogenic (e.g. are myogenic cells that are cultured in the cultivation infrastructure). Natively myogenic cells include, but are not limited to, myoblasts, myocytes, satellite cells, side population cells, muscle derived stem cells, mesenchymal stem cells, myogenic pericytes, or mesoangioblasts. In other embodiments, the myogenic cells are not natively myogenic (e.g. are non-myogenic cells that are specified to become myogenic cells in the cultivation infrastructure). In some embodiments, non-myogenic cells include embryonic stem cells, induced pluripotent stem cells, extraembryonic cell lines, and somatic cells other than muscle cells.

In some embodiments, non-myogenic cells are modified to become myogenic cells through the expression of one or more myogenic transcription factors. In exemplary embodiments, the myogenic transcription factor is MYOD1, MYOG, MYF5, MYF6, PAX3, PAX7, paralogs, orthologs, or genetic variants thereof.

In some embodiments, cells are modified to extend their renewal capacity through inactivation of cyclin-dependent kinase inhibitor (CKI) proteins and/or activation of Telomerase reverse transcriptase (TERT). Accordingly, in some embodiments, cells used in the methods of the present disclosure comprise a polynucleotide sequence expressing TERT. In some embodiments, cells used in the methods of the present disclosure comprise one or more loss-of-function mutations in the endogenous genes encoding CKI proteins. In some embodiments, cells comprise loss-of-function mutations in CKI proteins p15, p16, paralogs, orthologs, or genetic variants thereof. In some embodiments, cells used in the methods of the present disclosure comprise a polynucleotide sequence expressing TERT and one or more loss-of-function mutations in the endogenous genes encoding CKI proteins. The loss-of-function mutation may partially or completely inhibit the activity of CKI proteins.

In some embodiments, the process of extending the renewal capacity of the cells comprises activating Telomerase reverse transcriptase (TERT) activity in the cells and/or inactivating CKI proteins.

In some embodiments, the process of extending the renewal capacity of the cells comprises ectopic expression of TERT. In some embodiments, the process of extending the renewal capacity of the cells comprises introducing targeted mutations in the TERT promoter. In some embodiments, the process of extending the renewal capacity of the cells comprises activating endogenous TERT expression by an engineered transcriptional activator. In some embodiments, the process of extending the renewal capacity of the cells comprises transient transfection of TERT mRNA. In some embodiments, induction of endogenous pluripotency-associated telomerase activity in stem cells such as ESC and iPSC supports extended and indefinite cell renewal. In some embodiments, maintenance endogenous pluripotency-associated telomerase activity in stem cells such as ESC and iPSC supports extended and indefinite cell renewal.

In some embodiments, the process of extending the renewal capacity of the cells comprises inactivating one or more CKI proteins. In some embodiments, inactivating CKI proteins comprises introducing loss-of-function mutations in one or more genes encoding CKI proteins. In some embodiments, the loss-of-function mutation partially inhibits the activity of one or more CKI proteins. In some embodiments, the loss-of-function mutation completely inhibits the activity of one or more CKI proteins.

In some embodiments, the inactivation of CKI proteins and/or activation of TERT in the cells extend their renewal capacity for at least 25 population-doublings, at least 50 population-doublings, at least 60 population-doublings, at least 70 population-doublings, at least 80 population-doublings, at least 90 population-doublings, at least 100 population-doublings, at least 110 population-doublings, at least 120 population-doublings, at least 130 population-doublings, at least 140 population-doublings, at least 150 population-doublings, at least 160 population-doublings, at least 170 population-doublings, at least 180 population-doublings, at least 190 population-doublings, or at least 200 population-doublings. In some exemplary embodiments, the cells are primary myoblasts of a livestock, game, aquatic, or poultry species, whose renewal capacity is further extended.

In some embodiments, the cells are modified to inhibit HIPPO signaling, for example, by activating Yes-Associated Protein 1 (YAP1), Transcriptional co-Activator with PDZ-binding motif (TAZ), or a combination thereof in the cells.

In some embodiments, the cells are somatic cells. In some embodiments, the cells are not somatic cells.

In some embodiments, the cells are anchorage-dependent cells and are cultivated in on a substrate. In some embodiments, the cells are anchorage independent cells and are cultivated in a suspension culture. In some embodiments, the cells are cultivated in a suspension culture and form a self-adherent aggregate.

It is noted that the cells can be cultivated for any downstream application, not just limited to food production.

Cellular Modifications

Provided herein are compositions and methods to modify any one of the cells provided herein with a gene of interest in order to increase cell density of metazoan cells in a culture medium, decrease waste products, such as ammonia or ammonium hydroxide, decrease dependency on exogenous addition of factors such as glutamine, albumin, and IGF to the media and to provide a cultured edible product.

Glutamine Synthetase (GS)

Provided herein are cells that overexpress a GS protein.

Provided herein is a method of increasing the production of glutamine in cells or by cells, increasing glutamine secretion into culture medium, and/or decreasing the concentration of extracellular ammonia (to be used interchangeably with ammonium hydroxide where ammonium hydroxide is the form of ammonia present in an aqueous solution) in the medium of cells in culture, comprising increasing the expression of a glutamine synthetase (GS) protein in cells. Also provided herein is a method of increasing the cell density of metazoan cell in culture, comprising increasing the expression of GS in the cells in combination with other modifications described herein and culturing the cells in a cultivation infrastructure. Also provided is an in vitro method for producing a cultured edible product comprising increasing the expression of GS in the cells in combination with other modifications described herein.

In some embodiments, the cells are modified to overexpress a gene encoding a GS protein. In some embodiments, cells ectopically express a GS gene. In some embodiments, the cells are genetically modified and carry stable integrations of one or more copies of a GS gene. In some embodiments, the cells overexpress the gene encoding the GS protein at levels sufficient to decrease the ammonia production, increase the production of glutamine, or any combination thereof. In some embodiments, methods described herein to overexpress GS comprise introducing into the cells a polynucleotide sequence from Table 1B comprising a GS gene.

Increase of GS expression may be achieved using different approaches. In some embodiments, the expression is inducible. In some embodiments, the method comprises expressing nucleotides that encode the GS gene. In some embodiments, the nucleotides are ectopically expressed from constructs that are introduced into the cells, for example expressed from a plasmid, or other expression vector. In some embodiments, the constructs are integrated into the cell's genome, and the expression is driven in that manner (e.g. homologous recombination, introduction mediated by CRISPR-based technology). In some embodiments, expression of the GS gene involves electroporating a DNA, delivering a DNA complexed with a transfection vehicle, using a viral vector (e.g. retrovirus, lentivirus, adenovirus, adeno-associated virus, herpes simplex virus), and the like, or combinations thereof. In some embodiments, the expression is constitutive. In some embodiments, the expression is conditional, e.g. inducible, e.g. under the control of an inducible promoter, e.g. an inducible Tet construct. In some embodiments, the expression of GS is constitutive, but the expression of additional genes of interest is inducible. In some embodiments, the expression of GS is inducible, but the expression of additional genes of interest is constitutive.

In the methods described herein, a polynucleotide sequence encoding the GS gene may encode any homolog of GS, including GS paralogs, or a GS protein translated from any splice variants of a GS gene, or may comprise any mutations in the GS gene sequence including, but not limited to nucleotide deletions, truncations, fusions, or substitutions. Mutations may be synthetic or naturally occurring.

The GS gene can be from of any organism. The GS gene can be from bacteria, plants, fungi, and archaea. The GS gene can be from any animal, such as vertebrate and invertebrate animal species. The GS gene can be from any vertebrate animal species such as mammals, reptiles, birds, amphibians, and the like. The GS gene can be from any mammalian species such as a human, murine, bovine, porcine, and the like.

In some embodiments, the cells are of a livestock, poultry, game or aquatic animal species. In an exemplary embodiment, the renewal capacity of the primary duck myoblasts are extended, and the myoblasts are engineered to stably overexpress GS. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts are extended, and the myoblasts are engineered to transiently overexpress GS. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts are extended and are engineered to ectopically overexpress GS.

In some embodiments, the synthesis of glutamine by the cells is increased by at least 2.5%, by at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100%, at least 110%, at least 120%, at least 130%, at least 140%, at least 150%, at least 160%, at least 170%, at least 180%, at least 190%, at least 200%, at least 225%, at least 250%, at least 275%, at least 300%, at least 325%, at least 350%, at least 375% at least 400%, at least, 425%, at least 450%, at least 475%, at least 500%, at least 550%, at least 600%, at least 650%, at least 700%, at least 750%, at least 800%, at least 850%, at least 900%, at least 950% at least 1,000%, at least 1,100%, at least 1,200%, at least 1,300%, at least 1,400%, at least 1,500%, at least 1,600%, at least 1,700%, at least 1,800%, at least 1,900%, at least 2,000%, at least 2,250%, at least 2,500%, at least 2,750%, at least 3,000%, at least 3,500%, at least 4,000%, at least 4,500%, at least 5,000%, at least 6,000%, at least 7,000%, at least 8,000%, at least 9,000%, or even by at least 10,000%, including values and ranges therebetween, compared to cultures of cells in which glutamine synthesis is not increased by expression of GS as described herein.

In some embodiments, increased expression of GS using the methods described herein increases the concentration of glutamine in the culture medium to at least 0.001 mM, to at least 0.0025 mM, to at least 0.005 mM, to at least 0.0075 mM, to at least 0.01 mM, to at least 0.025 mM, to at least 0.05 mM, to at least 0.075 mM, to at least 0.1 mM, at least 0.25 mM, to at least 0.50 mM, to at least 0.75 mM, to at least 1.0 mM, to at least 1.5 mM, to at least 2.0 mM, to at least 3.0 mM, to at least 5.0 mM, to at least 10 mM, or even to at least 20 mM, including values and ranges therebetween, compared to cultures of cells in which the expression of GS is not increased.

Methods to measure the increase in the concentration of intracellular glutamine production include, but are not limited to assessment of the glutamine concentration in lysates of cell biomass or the ambient culture medium by HPLC (Chorili et. al., 2012. Validation of a HPLC Method for Determination of Glutamine in Food Additives Using Post-Column Derivatization, AJAC Vol. 3 No. 2) commercially available kits for absolute glutamine determination kits (Sigma-Aldrich #GLN1 and #GLN2), and trace-labeled (H³ radiolabeled) glutamine monitoring.

In some embodiments, the protein synthesis in the cells is increased by at least 2.5%, by at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, or even by at least 95%.

In some embodiments, the concentration of ammonia is decreased by at least 2.5%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, or even at least 95%. Methods to measure the decrease of extracellular ammonia concentrations in the cell media include, but are not limited to commercially available absolute ammonia detection kits such as (Sigma-Aldrich #AA0100), diffuse reflectance-based fiberoptic ammonia sensors (Non-enzymatic reversible colorimetric method such as diffuse reflectance-based fiberoptics (Spear, S. K., Rhiel, M., Murhammer, D. W. et al. Appl Biochem Biotechnol (1998) 75: 175), and use of a biochemistry analyzer (e.g. YSI Biochemistry Analyzer 2700).

In some embodiments, there is a delay in time for the cells to reach the ammonia concentration of otherwise not manipulated cultures (the wild-type cell ammonia concentration). For example, cells overexpressing GS may demonstrate at least a 1.5-fold, 2-fold, 3-fold, 4-fold, 5-fold, 6-fold, 7-fold, 8-fold, 9-fold, 10-fold, 15-fold, 20-fold, 25-fold, 30-fold, 40-fold, or even at least a 50-fold delay in time to achieve the wild type cell ammonia concentration.

In some embodiments, provided herein is a method of increasing the cell density of a culture comprising metazoan cells, comprising increasing the expression of glutamine synthetase (GS) protein by the cells, wherein the cells are of livestock, poultry, game or aquatic animal species. The culture density of cells may reach about 10⁵ cells/mL, about 10⁶ cells/mL, about 10⁷ cells/mL, about 10⁸ cells/mL, about 10⁹ cells/mL, or about 10¹⁰ cells/mL (cells in the cellular biomass/mL of cultivation infrastructure), including values and ranges therebetween.

In some embodiments, provided herein is a method of decreasing cell death comprising increasing the expression of glutamine synthetase in the cells. In some embodiments, the decrease in cell death is about 2.5%, about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, or about 100%, including values and ranges therebetween, compared to the methods where the expression of GS is not increased.

Insulin-Like Growth Factor (IGF)

Provided herein are cells that overexpress an IGF protein.

Provided herein is a method of increasing the production and secretion of IGF by cells comprising increasing the expression of an IGF protein in cells. Also provided herein is a method of increasing the cell density of a culture comprising metazoan cells comprising increasing the expression of IGF in the cells in combination with other modifications described herein and culturing the cells in a cultivation infrastructure. Also provided is an in vitro method for producing a cultured edible product comprising increasing the expression of GS in the cells in combination with other modifications described herein.

In some embodiments, the cells are modified to overexpress the gene encoding an IGF protein. In some embodiments, cells ectopically express the IGF gene. In some embodiments, the cells are genetically modified and carry stable integrations of one or more copies of an IGF gene. In some embodiments, the cells overexpress the gene encoding the IGF protein at levels sufficient to increase production and/or secretion of IGF into the cell medium. The IGF gene can be of any metazoan species.

Increase of IGF expression may be achieved using different approaches. In some embodiments, the expression is inducible. In some embodiments, the method comprises expressing nucleotides that encode the IGF gene. In some embodiments, the nucleotides are ectopically expressed from constructs that are introduced into the cells, for example expressed from a plasmid, or other expression vector. In some embodiments, the constructs are integrated into the cell's genome, and the expression is driven in that manner (e.g. homologous recombination, introduction mediated by CRISPR-based technology). In some embodiments the expression of the IGF gene involves electroporating a DNA, delivering a DNA complexed with a transfection vehicle, using a viral vector (e.g. retrovirus, lentivirus, adenovirus, adeno-associated virus, herpes simplex virus), and the like, or combinations thereof. In some embodiments, the expression is constitutive. In some embodiments, the expression is conditional, e.g. inducible, e.g. under the control of an inducible promoter, e.g. an inducible Tet construct. In some embodiments, the expression of IGF is constitutive, but the expression of additional genes of interest is inducible. In some embodiments, the expression of IGF is inducible, but the expression of additional genes of interest is constitutive.

The IGF gene can be from any animal, such as vertebrate and invertebrate animal species. The IGF gene can be from any vertebrate animal species such as mammals, reptiles, birds, amphibians, and the like. The IGF gene can be from any mammalian species such as a human, murine, bovine, porcine, poultry, and the like.

In the methods described herein, a polynucleotide sequence encoding the IGF gene may encode any homolog of IGF, including IGF paralogs, such as IGF-1, IGF-2 or any other IGF paralogs, or an IGF protein translated from any splice variants of an IGF gene, or may comprise any mutations in the IGF gene sequence including, but not limited to nucleotide deletions, truncations, fusions, or substitutions. Mutations may be synthetic or naturally occurring. In one embodiment, the methods described herein comprise introducing into the cells a polynucleotide sequence encoding IGF-1. In another embodiment, the methods described herein comprise introducing into the cells a polynucleotide sequence encoding IGF-2. In some embodiments, methods described herein to overexpress IGF comprise introducing into the cells a polynucleotide sequence from Table 1B comprising an IGF gene.

In some embodiments, the cells are of a livestock, poultry, game or aquatic animal species. In an exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to stably overexpress IGF. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to transiently overexpress IGF. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to ectopically overexpress IGF.

In some embodiments, the concentration of IGF in the cell culture medium is increased by at least 0.001%, 0.005%, 0.01%, at least 0.02%, at least 0.03%, at least 0.04%, at least 0.05%, at least 0.075%, at least 0.1%, at least 0.5%, at least 0.75%, at least 1%, at least 1.25%, at least 1.5%, at least 1.75%, at least 2%, at least 2.5%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100%, at least 110%, at least 120%, at least 130%, at least 140%, at least 150%, at least 160%, at least 170%, at least 180%, at least 190%, at least 200%, at least 225%, at least 250%, at least 275%, at least 300%, at least 325%, at least 350%, at least 375% at least 400%, at least, 425%, at least 450%, at least 475%, at least 500%, at least 550%, at least 600%, at least 650%, at least 700%, at least 750%, at least 800%, at least 850%, at least 900%, at least 950% at least 1,000%, at least 1,100%, at least 1,200%, at least 1,300%, at least 1,400%, at least 1,500%, at least 1,600%, at least 1,700%, at least 1,800%, at least 1,900%, at least 2,000%, at least 2,250%, at least 2,500%, at least 2,750%, at least 3,000%, at least 3,500%, at least 4,000%, at least 4,500%, at least 5,000%, at least 6,000%, at least 7,000%, at least 8,000%, at least 9,000%, or even by at least 10,000% including values and ranges therebetween, compared to cultures of cells in which the expression of IGF is not increased as described herein.

In some embodiments, increased expression of IGF using the methods described herein increases the concentration of IGF in the culture medium by at least 0.00001 ng/mL, to at least 0.000025 ng/mL, to at least 0.000075 ng/mL, to at least 0.0005 ng/mL, to at least 0.001 ng/mL, to at least 0.0025 ng/mL, to at least 0.005 ng/mL, to at least 0.0075 ng/mL, to at least 0.01 ng/mL, to at least 0.025 ng/mL, to at least 0.05 ng/mL, to at least 0.1 ng/mL, to at least 0.25 ng/mL, to at least 0.5 ng/mL, to at least 1 ng/mL, to at least 2.5 ng/mL, to at least 5 ng/mL, to at least 7.5 ng/mL, to at least 10 ng/mL, to at least 25 ng/mL, to at least 50 ng/mL, to at least 75 ng/mL, to at least 125 ng/mL, to at least 250 ng/mL, to at least 500 ng/mL, to at least 750 ng/mL, to at least 1,000 ng/mL, to at least 1,500 ng/mL, to at least 2,000 ng/mL, to at least 2,500 ng/mL, to at least 3,000 ng/mL, to at least 3,500 ng/mL, to at least 4,000 ng/mL, to at least 4,500 ng/mL, to at least 5,000 ng/mL to at least 6,000 ng/mL, to at least 7,000 ng/mL, to at least 8,000 ng/mL, to at least 9,000 ng/mL, or even to at least 10,000 ng/mL including values and ranges therebetween, compared to cultures of cells in which the expression of IGF is not increased as described herein.

Methods to measure the increase in the concentration of IGF include, but are not limited to, antibody-based methods such as immunoprecipitation, co-immunoprecipitation, Western blotting, Enzyme-linked immunosorbent assay (ELISA), and amino-acid based tagging, isolation, and separation (e.g., FLAG, GST, GFP, etc.).

In some embodiments, the rate of synthesis of IGF by cells is increased by about 0.000001 μg/10⁶ cells/day, by about 0.00001 μg/10⁶ cells/day, by about 0.0001 μg/10⁶ cells/day, 0.001 μg/10⁶ cells/day, by about 0.01 μg/10⁶ cells/day, by about 0.1 μg/10⁶ cells/day, by about 1.0 μg/10⁶ cells/day, by about 10 μg/10⁶ cells/day, by about 100 μg/10⁶ cells/day, by about 10 μg/10⁶ cells/day, by about 100 μg/10⁶ cells/day, by about 1,000 μg/10⁶ cells/day, or by even about 10,000 μg/10⁶ cells/day, including values and ranges therebetween, compared to cells wherein the rate of IGF synthesis is not increased as described herein.

In some embodiments, provided herein is a method of increasing the proliferation rate of cells comprising increasing the expression of Insulin-like Growth Factor (IGF) protein by the cells, wherein the cells are of livestock, poultry, game or aquatic animal species. In some embodiments, the population doubling time of the cells is decreased by about by about 5%, by about 10%, by about 15%, by about 20%, by about 25%, by about 30%, by about 35%, by about 40%, by about 45%, by about 50%, by about 55%, by about 60%, by about 65%, by about 70%, by about 75%, by about 80%, by about 85%, by about 90%, by about 95%, or by more than 95%, including values and ranges therebetween, compared to cells wherein the expression of IGF is not increased.

In some embodiments, provided herein is a method of increasing protein production in the cells comprising increasing the expression of Insulin-like Growth Factor (IGF) protein by the cells, wherein the cells are of livestock, poultry, game or aquatic animal species. In some embodiments, the protein produced by the cells in culture is measured as total cell protein per cell nucleus. In some embodiments, the total cell protein per nucleus is increased by about 5%, by about 10%, by about 15%, by about 20%, by about 25%, by about 30%, by about 35%, by about 40%, by about 45%, by about 50%, by about 55%, by about 60%, by about 65%, by about 70%, by about 75%, by about 80%, by about 85%, by about 90%, by about 95%, by about 100%, by about 110%, by about 120%, by about 130%, by about 140%, by about 150%, by about 160%, by about 170%, by about 180%, by about 190%, by about 200%, by about 225%, by about 250%, by about 275%, by about 300%, by about 350%, by about 400%, by about 450%, by about 500%, by about 550%, by about 600%, by about 650%, by about 700%, by about 750%, by about 800%, by about 850%, by about 900%, by about 950%, by about 1,000%, by about 1,100%, by about 1,200%, by about 1,300%, by about 1,400%, by about 1,500%, by about 1,600%, by about, 1,700%, by about 1,800%, by about 1,900%, by about 2,000%, by about 2,100%, by about 2,200%, by about 2,300%, by about 2,400%, by about 2,500%, by more than 2,500%, including values and ranges therebetween, compared to the total cell protein production where the expression of IGF is not increased.

In some embodiments, the total cell protein per nucleus is increased by about 5 pg/nucleus; by about 10 pg/nucleus; by about 15 pg/nucleus; by about 20 pg/nucleus; by about 25 pg/nucleus; by about 30 pg/nucleus; by about 35 pg/nucleus; by about 40 pg/nucleus; by about 45 pg/nucleus, by about 50 pg/nucleus; by about 55 pg/nucleus, by about 60 pg/nucleus, by about 65 pg/nucleus, by about 70 pg/nucleus, by about 75 pg/nucleus, by about 80 pg/nucleus, by about 85 pg/nucleus, by about 90 pg/nucleus, by about 95 pg/nucleus, by about 100 pg/nucleus, by about 110 pg/nucleus, by about 120 pg/nucleus, by about 130 pg/nucleus, by about 140 pg/nucleus, by about by about 150 pg/nucleus, by about, by about 160 pg/nucleus, by about 170 pg/nucleus, by about 180 pg/nucleus, by about 190 pg/nucleus, by about 200 pg/nucleus, by about 225 pg/nucleus, by about 250 pg/nucleus, by about 275 pg/nucleus, by about 280 pg/nucleus, by about 290 pg/nucleus, by about 300 pg/nucleus, by about 350 pg/nucleus, by about 400 pg/nucleus, by about 450 pg/nucleus, by about 500 pg/nucleus, by about 550 pg/nucleus, by about 600 pg/nucleus, by about 650 pg/nucleus, by about 700 pg/nucleus, by about 750 pg/nucleus, by about 800 pg/nucleus, by about 850 pg/nucleus, by about 900 pg/nucleus, by about 950 pg/nucleus, by about 1000 pg/nucleus, by about 1,100 pg/nucleus, by about 1,200 pg/nucleus, by about 1,300 pg/nucleus, by about 1,400 pg/nucleus, by about 1,500 pg/nucleus, by about 1,600 pg/nucleus, by about 1,700 pg/nucleus, by about 1,800 pg/nucleus, by about 1,900 pg/nucleus, by about 2,000 pg/nucleus, by about 2,100 pg/nucleus, by about 2,200 pg/nucleus, by about 2,300 pg/nucleus, by about 2,400 pg/nucleus, by about 2,500 pg/nucleus, by more than 2,500 pg/nucleus, including values and ranges therebetween.

In some embodiments, provided herein is a method for increasing the rate of proliferation of cells in a cultivation infrastructure, comprising increasing the expression of Insulin-like Growth Factor (IGF) protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species. In some embodiments, increasing the expression of IGF comprises introducing a polynucleotide sequence encoding IGF into the cells. In some embodiments, the polynucleotide sequence encodes IGF1. In some embodiments, the polynucleotide sequence encodes IGF2. In some embodiments, the polynucleotide sequence comprises an IGF coding sequence from Tables 1A and 1B.

Albumin

Provided herein are cells that overexpress an albumin protein.

Provided herein is a method of increasing the production and secretion of albumin by cells comprising increasing the expression of an albumin protein in the cells. Also provided herein is a method of increasing the cell density of a culture comprising metazoan cells, comprising increasing the expression of albumin in the cells in combination with other modifications described herein and culturing the cells in a cultivation infrastructure. Also provided is an in vitro method for producing a cultured edible product comprising increasing the expression of albumin in the cells in combination with other modifications described herein.

In some embodiments, the cells are modified to overexpress the gene encoding albumin. In some embodiments, cells ectopically express the albumin gene. In some embodiments, the cells are genetically modified and carry stable integrations of one or more copies of the albumin gene. In some embodiments, the cells overexpress the gene encoding the albumin protein at levels sufficient to increase production and/or secretion of albumin into the cell culture medium.

Increase of albumin expression may be achieved using different approaches. In some embodiments, the expression is inducible. In some embodiments, the method comprises expressing nucleotides that encode the albumin gene. In some embodiments, the nucleotides are ectopically expressed from constructs that are introduced into the cells, for example expressed from a plasmid, or other expression vector. In some embodiments, the constructs are integrated into the cell's genome, and the expression is driven in that manner (e.g. homologous recombination, introduction mediated by CRISPR-based technology). In some embodiments, expression of the albumin gene involves electroporating a DNA, delivering a DNA complexed with a transfection vehicle, using a viral vector (e.g. retrovirus, lentivirus, adenovirus, adeno-associated virus, herpes simplex virus), and the like, or combinations thereof. In some embodiments, the expression is constitutive. In some embodiments, the expression is conditional, e.g. inducible, e.g. under the control of an inducible promoter, e.g. an inducible Tet construct. In some embodiments, the expression of albumin is constitutive, but the expression of additional genes of interest is inducible. In some embodiments, the expression of albumin is inducible, but the expression of additional genes of interest is constitutive.

The albumin gene can be from any animal, such as vertebrate and invertebrate animal species. In some embodiments, the albumin gene can be from any vertebrate animal species such as mammals, reptiles, birds, amphibians, and the like. In some embodiments, the albumin gene can be from any mammalian species, such as a human, murine, bovine, porcine, livestock, and the like.

In the methods described herein, a polynucleotide sequence encoding the albumin gene may encode any homolog of albumin, including any albumin paralogs, or an albumin protein translated from any splice variants of an albumin gene, or may comprise any mutations in the albumin gene sequence including, but not limited to nucleotide deletions, truncations, fusions, or substitutions. Mutations may be synthetic or naturally occurring. In some embodiments, methods described herein to overexpress albumin comprise introducing into the cells a polynucleotide sequence from Table 1B comprising an albumin gene.

In some embodiments, the cells are of a livestock, poultry, game or aquatic animal species. In an exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to stably overexpress albumin. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to transiently overexpress albumin. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to ectopically overexpress albumin.

In some embodiments, an increased expression of albumin using the methods described herein increases the concentration of albumin in the culture medium by at least 0.001%, 0.005%, 0.01%, at least 0.02%, at least 0.03%, at least 0.04%, at least 0.05%, at least 0.075%, at least 0.1%, at least 0.5%, at least 0.75%, at least 1%, at least 1.25%, at least 1.5%, at least 1.75%, at least 2%, at least 2.5%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100%, at least 110%, at least 120%, at least 130%, at least 140%, at least 150%, at least 160%, at least 170%, at least 180%, at least 190%, at least 200%, at least 225%, at least 250%, at least 275%, at least 300%, at least 325%, at least 350%, at least 375% at least 400%, at least, 425%, at least 450%, at least 475%, at least 500%, at least 550%, at least 600%, at least 650%, at least 700%, at least 750%, at least 800%, at least 850%, at least 900%, at least 950% at least 1,000%, at least 1,100%, at least 1,200%, at least 1,300%, at least 1,400%, at least 1,500%, at least 1,600%, at least 1,700%, at least 1,800%, at least 1,900%, at least 2,000%, at least 2,250%, at least 2,500%, at least 2,750%, at least 3,000%, at least 3,500%, at least 4,000%, at least 4,500%, at least 5,000%, at least 6,000%, at least 7,000%, at least 8,000%, at least 9,000%, or even by at least 10,000% including values and ranges therebetween, compared to cultures of cells in which the albumin expression is not increased as described herein.

In some embodiments, an increased expression of albumin using the methods described herein increases the concentration of albumin in the culture medium to at least 0.0001 mg/mL, to at least 0.0002 mg/mL, to at least 0.0004 mg/mL, to at least 0.0005 mg/mL, to at least 0.0006 mg/mL, to at least 0.0007 mg/mL, to at least 0.0008 mg/mL, to at least 0.0009 mg/mL, to at least 0.001 mg/mL, to at least 0.002 mg/mL, to at least 0.003 mg/mL, to at least 0.004 mg/mL, to at least 0.005 mg/mL, to at least 0.006 mg/mL, to at least 0.007 mg/mL, to at least 0.008 mg/mL, to at least 0.009 mg/mL, to at least 0.01 mg/mL, to at least 0.05 mg/mL, to at least 0.075 mg/mL, to at least 0.1 mg/mL, to at least 0.25 mg/mL, to at least 0.5 mg/mL, to at least 0.75 mg/mL, to at least 1 mg/mL, to at least 1.25 mg/mL, to at least 1.5 mg/mL, to at least 1.75 mg/mL, to at least 2 mg/mL, to at least 3 mg/mL, to at least 5 mg/mL, to at least 10 mg/mL, to at least 20 mg/mL, to at least 25 mg/mL, to at least 50 mg/mL, to at least 75 mg/mL, or even to at least 100 mg/mL, including values and ranges therebetween, compared to cultures of cells in which the albumin expression is not increased as described herein.

Methods to measure the increase in the concentration of albumin include commercial kits, such as the BCG Albumin Assay Kit (Sigma-Aldrich #MAK124), BCP Albumin Assay Kit (Sigma-Aldrich #MAK125), and antibody-based methods, such as immunoprecipitation, co-immunoprecipitation, Western blotting, Enzyme-linked immunosorbent assay (ELISA), and amino-acid based tagging, isolation, and separation (e.g., FLAG, GST, GFP, etc.).

In some embodiments, provided herein is a method of increasing the rate of proliferation of cells in a cultivation infrastructure, comprising increasing the expression of albumin in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species. In some embodiments, the population doubling time of the cells is decreased by about 10%, by about 15%, by about 20%, by about 25%, by about 30%, by about 35%, by about 40%, by about 45%, by about 50%, by about 55%, by about 60%, by about 65%, by about 70%, by about 75%, by about 80%, by about 85%, by about 90%, by about 95%, by more than 95%, including values and ranges therebetween, compared to cells in which the expression of albumin is not increased.

In one embodiment, provided herein is a method of decreasing cell death comprising increasing the expression of albumin in the cells. In some embodiments, the decrease in cell death provided is about 2.5%, about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, or about 100%, including values and ranges therebetween, compared to the methods wherein the expression of albumin is not increased.

In some embodiments, provided herein are cells that overexpress any combination of GS, IGF, and albumin. For example, in one embodiment, provided herein are cells that overexpress a GS protein and an IGF protein. In one embodiment, provided herein are cells that overexpress an albumin protein and a GS protein. In one embodiment, provided herein are cells that overexpress an albumin protein and an IGF protein. In one embodiment, provided herein are cells that overexpress an albumin protein, a GS protein, and an IGF protein.

TERT and CKI Proteins

Provided herein are cells whose renewal capacity is extended, for e.g., by overexpressing a TERT protein and/or by inhibiting the activity of CKI proteins. Exemplary methods to overexpress TERT and inhibit the activity of CKI proteins are disclosed in U.S. Provisional Application No. 62/278,869, filed on Jan. 14, 2016, and 62/361,867, filed on Jul. 13, 2016, and a PCT Application No. PCT/US2017/013782, filed on Jan. 17, 2017, all of which are incorporated herein by reference in their entirety.

In some embodiments, provided herein is a method for increasing the density of cells in a culture or an in vitro method for producing a cultured edible product comprising increasing the expression of a TERT protein in the cells in combination with increasing the expression of GS, IGF, albumin, or a combination thereof. In some embodiments, provided herein is a method for increasing the density of cells in a culture or an in vitro method for producing a cultured edible product comprising inhibiting the activity of CKI proteins in the cells in combination with increasing the expression of GS, IGF, albumin, or a combination thereof. In some embodiments, provided herein is a method for increasing the density of cells in a culture or an in vitro method for producing a cultured edible product comprising increasing the expression of a TERT protein in the cells, inhibiting the activity of CKI proteins in the cells, and increasing the expression of GS, IGF, albumin, or a combination thereof.

In some embodiments, the cells are modified to overexpress a polynucleotide sequence encoding TERT. In some embodiments, cells ectopically express the TERT polynucleotide. In some embodiments, the cells are genetically modified and carry stable integrations of one or more copies of the TERT polynucleotide.

Increased expression of TERT may be achieved using different approaches. In some embodiments, increased expression of TERT may be achieved by ectopically expressing TERT. In some embodiments, increased expression of TERT may be achieved by introducing targeted mutations in the TERT promoter. In some embodiments, increased expression of TERT may be achieved by activating endogenous TERT expression by an engineered transcriptional activator. In some embodiments, increased expression of TERT may be achieved by transiently transfecting TERT mRNA.

In some embodiments, the expression of TERT is inducible. In some embodiments, the method comprises expressing nucleotides that encode the TERT protein. In some embodiments, the nucleotides are ectopically expressed from constructs that are introduced into the cells, for example expressed from a plasmid, or other expression vector. In some embodiments, the constructs are integrated into the cell's genome, and the expression is driven in that manner (e.g. homologous recombination, introduction mediated by CRISPR-based technology). In some embodiments, the expression of the TERT gene involves electroporating a DNA, delivering a DNA complexed with a transfection vehicle, using a viral vector (e.g. retrovirus, lentivirus, adenovirus, adeno-associated virus, herpes simplex virus), and the like, or combinations thereof. In some embodiments, the expression is constitutive. In some embodiments, the expression is conditional, e.g. inducible, e.g. under the control of an inducible promoter, e.g. an inducible Tet construct. In some embodiments, the expression of TERT is constitutive, but the expression of additional genes of interest is inducible. In some embodiments, the expression of TERT is inducible, but the expression of additional genes of interest is constitutive.

The polynucleotide encoding TERT can be from of any organism. The TERT polynucleotide can be from bacteria, plants, fungi, and archaea. The TERT polynucleotide can be from any animal, such as vertebrate and invertebrate animal species. The TERT polynucleotide can be from any vertebrate animal species such as mammals, reptiles, birds, amphibians, and the like. The TERT polynucleotide can be from any mammalian species, such as a human, murine, bovine, porcine, and the like.

In some embodiments, the methods of inhibiting CKI proteins comprise introducing loss-of-function mutations, e.g., INDEL (insertion or deletion) mutations, into one or more genes encoding CKI proteins in the cells. This can be accomplished using any gene based technologies, for example, using CRISPR-Cas (Clustered Regularly Interspersed Short Palindromic Repeats) based technology or TALEN based technology. In an exemplary embodiment, the genes encoding CKI proteins are the genes encoding CKI proteins p15, p16, paralogs, orthologs, or genetic variants thereof. In an exemplary embodiment, the methods of inhibiting CKI proteins comprise introducing loss-of-function mutations in CDKN2B gene (p15) and/or in CDKN2A gene (p16).

In some embodiments, inhibiting the activity of CKI proteins comprises activating a CDK4 protein, paralogs, orthologs or genetic variants thereof.

In some embodiments, the methods of inhibiting the CKI function comprise introducing into the cells a vector expressing a polynucleotide that encodes a dominant negative mutant of one or more CKI proteins. In some embodiments, the polynucleotide is ectopically expressed from a construct that is introduced into the cells of the biomass, for example expressed from a plasmid, or other vector. In some embodiments, the construct is integrated into the cell's genome, and the expression is driven in that manner (e.g. introduction mediated by CRISPR-based technology). In some embodiments, the expression of the polynucleotide involves electroporating a DNA, delivering a DNA complexed with a transfection vehicle, using a viral vector (e.g. retrovirus, lentivirus, adenovirus, adeno-associated virus, herpes simplex virus), and the like, or combinations thereof. In some embodiments, the expression is constitutive. In some embodiments, the expression is conditional, e.g. inducible, e.g. under the control of an inducible promoter, e.g. an inducible Tet construct.

In some embodiments, the methods of inhibiting comprise delivering dominant negative mutants of one or more CKI proteins directly, e.g. purified proteins, synthetic proteins, or recombinantly expressed proteins, or combinations thereof, to the cells.

In some embodiments, the methods of inhibiting comprise transcriptional repression of the endogenous genes encoding one or more CKI proteins in the cells. This can be accomplished, for example, by using nucleic acid sequence-directed transcriptional repressors. For example, an endonuclease-defective Cas9, dCas9, can be combined with a guide RNA that targets the promoter region of the genes encoding one or more CKI proteins and reduces the transcriptional activation and concomitant gene expression.

In some embodiments, the cells are of a livestock, poultry, game or aquatic animal species. In an exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to stably overexpress GS, IGF, albumin, or any combination thereof. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to transiently overexpress GS, IGF, albumin, or any combination thereof. In another exemplary embodiment, the renewal capacity of the primary duck myoblasts is extended, and the myoblasts are engineered to ectopically overexpress GS, IGF, albumin, or any combination thereof.

In some embodiments, provided herein are cells that overexpress a GS protein and an IGF protein. The cells may optionally be modified to extend renewal capacity, and may comprise activated TERT and/or inactivated CKI protein, may comprise an antagonized HIPPO signaling pathway, e.g., activated YAP/TAZ, may be further differentiated, and the like.

In some embodiments, provided herein are cells that overexpress an albumin protein and a GS protein. The cells may optionally be modified to extend renewal capacity, and may comprise activated TERT and/or inactivated CKI protein, may comprise an antagonized HIPPO signaling pathway, e.g., activated YAP/TAZ, may be further differentiated, and the like.

In some embodiments, provided herein are cells that overexpress an albumin protein and an IGF protein. The cells may optionally be modified to extend renewal capacity, and may comprise activated TERT and/or inactivated CKI protein, may comprise an antagonized HIPPO signaling pathway, e.g., activated YAP/TAZ, may be further differentiated, and the like.

In some embodiments, provided herein are cells that overexpress an albumin protein, a GS protein, and an IGF protein. The cells may optionally be modified to extend renewal capacity, and may comprise activated TERT and/or inactivated CKI protein, may comprise an antagonized HIPPO signaling pathway, e.g., activated YAP/TAZ, may be further differentiated, and the like.

Tables 1A and 1B show exemplary sequences used for ectopic overexpression in some exemplary embodiments provided herein. The cells may optionally be modified to extend renewal capacity, and may comprise activated TERT and/or inactivated CKI protein, may comprise an antagonized HIPPO signaling, e.g., activated YAP/TAZ, may be further differentiated, and the like.

Table 1C shows exemplary amino acid sequences for GS, albumin, and IGF proteins that may be expressed in cells according to the methods described here.

TABLE 1A
				Eukaryotic	Prokaryotic
		NCBI		selection	selection
Gene	Species	#	Vendor	marker	marker	Tag	Backbone
Glutamine	mouse	NM_008131	Genscript	Neo	Amp	C terminal	pcDNA3.1+/
Synthetase			OMu19897D			DYKDDD	C-(K)DYK
(GS)						DK (SEQ	(SEQ ID
						ID NO: 57)	NO: 58)
						tags
IGF-1	human	NM_000618.2	Origene	Neo	Kan	Myc-DDK	pCMV6-
			RG212527				Entry
Albumin	human	NM_000477	Genscript	Neo	Amp	C terminal
			OHu18744			DYKDDD
						DK (SEQ
						ID NO: 57)
						tags
Albumin	Mouse	NM_009654	Genscript	Neo	Amp	C terminal
			OMu21640			DYKDDD
						DK (SEQ
						ID NO: 57)
						tags

TABLE 1B
Gene	Species	NCBI #	DNA Sequence
IGF1 +	bovine		ATGAAGTGGGTGACTTTTATTTCCCTTCTCTTTCTCT
porcine			TCAGCTCTGCTTATTCCTTCTTGAAGCAGGTGAAGA
albumin			TGCCCATCACATCCTCCTCGCATCTCTTCTATCTGG
signal			CCCTGTGCTTGCTCGCCTTCACCAGCTCTGCCACGG
peptide			CGGGACCCGAGACCCTCTGCGGGGCTGAGTTGGTG
			GATGCTCTCCAGTTCGTGTGCGGAGACAGGGGCTT
			TTATTTCAACAAGCCCACGGGGTATGGCTCGAGCA
			GTCGGAGGGCGCCCCAGACAGGAATCGTGGATGA
			GTGCTGCTTCCGGAGCTGTGATCTGAGGAGGCTGG
			AGATGTACTGCGCGCCTCTCAAGCCCGCCAAGTCG
			GCCCGCTCAGTCCGTGCCCAGCGCCACACCGACAT
			GCCCAAGGCTCAGAAGGAAGTACATTTGAAGAACA
			CAAGTAGAGGGAGTGCAGGAAACAAGAACTACAG
			AATGTAG (SEQ ID NO: 1)
IGF1 +	chicken		ATGAAGTGGGTGACTTTTATTTCCCTTCTCTTTCTCT
porcine			TCAGCTCTGCTTATTCCTTCTTGAAGGTGAAGATGC
albumin			ACACTGTGTCCTACATTCATTTCTTCTACCTTGGCC
signal			TGTGTTTGCTTACCTTAACCAGTTCTGCTGCTGCCG
peptide			GCCCAGAAACACTGTGTGGTGCTGAGCTGGTTGAT
			GCTCTTCAGTTCGTATGTGGAGACAGAGGCTTCTAC
			TTCAGTAAGCCTACAGGGTATGGATCCAGCAGTAG
			ACGCTTACACCACAAGGGAATAGTGGATGAATGCT
			GCTTCCAGAGTTGTGACCTGAGGAGGCTGGAGATG
			TACTGTGCTCCAATAAAGCCACCTAAATCTGCACG
			CTCTGTACGTGCTCAGCGCCACACTGATATGCCAA
			AAGCACAAAAGGAAGTGCATTTGAAGAATACAAG
			TAGAGGGAACACAGGAAACAGAAACTACAGAATG
			TAA (SEQ ID NO: 2)
IGF1 +	porcine		ATGAAGTGGGTGACTTTTATTTCCCTTCTCTTTCTCT
porcine			TCAGCTCTGCTTATTCCTTGGCCCTGTGCTTGCTCTC
albumin			CTTCACCAGCTCTGCCACGGCTGGACCTGAGACCC
signal			TCTGTGGGGCTGAGCTGGTGGACGCTCTTCAGTTCG
peptide			TGTGCGGAGACAGGGGCTTTTATTTCAACAAGCCC
			ACAGGGTACGGCTCCAGCAGTCGGAGGGCGCCACA
			GACGGGCATCGTGGATGAGTGCTGCTTCCGGAGCT
			GTGATCTGAGGAGGCTGGAGATGTACTGTGCACCC
			CTCAAGCCTGCCAAGTCGGCCCGCTCCGTCCGTGC
			CCAGCGCCACACGGACATGCCCAAGGCTCAGAAGG
			AAGTACATTTGAAGAACACAAGTAGAGGGAGTTCA
			GGAAACAAGAACTACAGAATGTAG (SEQ ID NO: 3)
Wild	chicken	NM_001004384	ATGGAAAAAATCAACAGTCTTTCAACACAATTAGT
Type			TAAGTGCTGCTTTTGTGATTTCTTGAAGGTGAAGAT
IGF1			GCACACTGTGTCCTACATTCATTTCTTCTACCTTGG
			CCTGTGTTTGCTTACCTTAACCAGTTCTGCTGCTGC
			CGGCCCAGAAACACTGTGTGGTGCTGAGCTGGTTG
			ATGCTCTTCAGTTCGTATGTGGAGACAGAGGCTTCT
			ACTTCAGTAAGCCTACAGGGTATGGATCCAGCAGT
			AGACGCTTACACCACAAGGGAATAGTGGATGAATG
			CTGCTTCCAGAGTTGTGACCTGAGGAGGCTGGAGA
			TGTACTGTGCTCCAATAAAGCCACCTAAATCTGCA
			CGCTCTGTACGTGCTCAGCGCCACACTGATATGCC
			AAAAGCACAAAAGGAAGTGCATTTGAAGAATACA
			AGTAGAGGGAACACAGGAAACAGAAACTACAGAA
			TGTAA (SEQ ID NO: 4)
Wild	bovine	NM_001077828	ATGGGAAAAATCAGCAGTCTTCCAACCCAATTATT
Type			TAAGTGCTGCTTTTGTGATTTCTTGAAGCAGGTGAA
IGF1			GATGCCCATCACATCCTCCTCGCATCTCTTCTATCT
			GGCCCTGTGCTTGCTCGCCTTCACCAGCTCTGCCAC
			GGCGGGACCCGAGACCCTCTGCGGGGCTGAGTTGG
			TGGATGCTCTCCAGTTCGTGTGCGGAGACAGGGGC
			TTTTATTTCAACAAGCCCACGGGGTATGGCTCGAG
			CAGTCGGAGGGCGCCCCAGACAGGAATCGTGGATG
			AGTGCTGCTTCCGGAGCTGTGATCTGAGGAGGCTG
			GAGATGTACTGCGCGCCTCTCAAGCCCGCCAAGTC
			GGCCCGCTCAGTCCGTGCCCAGCGCCACACCGACA
			TGCCCAAGGCTCAGAAGGAAGTACATTTGAAGAAC
			ACAAGTAGAGGGAGTGCAGGAAACAAGAACTACA
			GAATGTAG (SEQ ID NO: 5)
Wild	porcine	NM_214256	ATGCACATCACATCCTCTTCGCATCTCTTCTACTTG
Type			GCCCTGTGCTTGCTCTCCTTCACCAGCTCTGCCACG
IGF1			GCTGGACCTGAGACCCTCTGTGGGGCTGAGCTGGT
			GGACGCTCTTCAGTTCGTGTGCGGAGACAGGGGCT
			TTTATTTCAACAAGCCCACAGGGTACGGCTCCAGC
			AGTCGGAGGGCGCCACAGACGGGCATCGTGGATG
			AGTGCTGCTTCCGGAGCTGTGATCTGAGGAGGCTG
			GAGATGTACTGTGCACCCCTCAAGCCTGCCAAGTC
			GGCCCGCTCCGTCCGTGCCCAGCGCCACACGGACA
			TGCCCAAGGCTCAGAAGGAAGTACATTTGAAGAAC
			ACAAGTAGAGGGAGTTCAGGAAACAAGAACTACA
			GAATGTAG (SEQ ID NO: 6)
Albumin +	bovine		ATGAAGTGGGTGACTTTTATTTCCCTTCTCTTTCTCT
porcine			TCAGCTCTGCTTATTCCAGGGGTGTGTTTCGTCGAG
albumin			ATACACACAAGAGTGAGATTGCTCATCGGTTTAAA
signal			GATTTGGGAGAAGAACATTTTAAAGGCCTGGTACT
peptide			GATTGCCTTTTCTCAGTATCTCCAGCAGTGTCCATT
			TGATGAGCATGTAAAATTAGTGAACGAACTAACTG
			AGTTTGCAAAAACATGTGTTGCTGATGAGTCCCAT
			GCCGGCTGTGAGAAGTCACTTCACACTCTCTTTGGA
			GATGAATTGTGTAAAGTTGCATCCCTTCGTGAAAC
			CTATGGTGACATGGCTGACTGCTGTGAGAAACAAG
			AACCTGAGAGAAATGAATGCTTCTTGTCACACAAA
			GATGATAGCCCTGATCTACCTAAACTCAAACCTGA
			CCCCAATACTTTGTGTGACGAGTTTAAGGCCGATG
			AAAAGAAGTTTTGGGGAAAATACCTATACGAAATT
			GCTAGAAGACATCCCTACTTTTATGCACCAGAACT
			CCTTTACTATGCTAATAAATATAATGGAGTTTTTCA
			AGAATGCTGCCAAGCTGAAGATAAAGGTGCCTGCC
			TGCTACCAAAGATTGAAACTATGAGGGAAAAGGTA
			CTGACTTCATCTGCCAGACAGAGACTCAGGTGTGC
			CAGTATTCAAAAATTTGGAGAAAGAGCTTTAAAAG
			CATGGTCAGTAGCTCGCCTGAGCCAGAAATTTCCC
			AAGGCTGAGTTTGTAGAAGTTACCAAGCTAGTGAC
			AGATCTCACAAAAGTGCACAAGGAATGCTGCCATG
			GAGACCTACTTGAATGCGCAGATGACAGGGCGGAC
			CTTGCCAAGTACATATGTGATAATCAAGATACAAT
			CTCCAGTAAACTGAAGGAATGCTGTGATAAGCCTT
			TGTTGGAAAAATCCCACTGCATTGCTGAGGTAGAA
			AAAGATGCCATACCTGAAAACTTGCCCCCATTAAC
			TGCTGACTTTGCTGAAGATAAGGATGTATGCAAAA
			ACTATCAAGAAGCAAAGGATGCCTTCCTGGGCTCA
			TTTCTTTATGAATATTCAAGAAGGCATCCTGAATAT
			GCTGTCTCAGTGCTATTGAGACTTGCCAAGGAATA
			TGAAGCCACACTGGAGGAATGCTGTGCCAAAGATG
			ATCCACATGCATGCTATTCCACAGTGTTTGACAAAC
			TTAAGCATCTTGTGGATGAGCCTCAGAATTTAATTA
			AACAAAACTGTGACCAATTCGAAAAACTTGGAGAG
			TATGGATTCCAAAATGCGCTCATAGTTCGTTACACC
			AGGAAAGTACCCCAAGTGTCAACTCCAACTCTCGT
			GGAGGTTTCAAGAAGCCTAGGAAAAGTGGGTACTA
			GGTGTTGTACAAAACCGGAATCAGAAAGAATGCCC
			TGTACAGAAGACTATCTGAGCTTGATCCTGAACCG
			GTTGTGCGTGCTGCATGAGAAGACACCAGTGAGTG
			AAAAAGTCACCAAGTGCTGCACAGAGTCATTGGTG
			AACAGACGGCCATGTTTCTCTGCTCTGACACCTGAT
			GAAACATATGTACCCAAAGCCTTTGATGAGAAATT
			GTTCACCTTCCATGCAGATATATGCACACTTCCCGA
			TACTGAGAAACAAATCAAGAAACAAACTGCACTTG
			TTGAGCTGTTGAAACACAAGCCCAAGGCAACAGAG
			GAACAACTGAAAACCGTCATGGAGAATTTTGTGGC
			TTTTGTAGACAAGTGCTGCGCAGCTGATGACAAAG
			AAGCCTGCTTTGCTGTGGAGGGTCCAAAACTTGTT
			GTTTCAACTCAAACAGCCTTAGCCTAA (SEQ ID NO:
			7)
Albumin +	chicken		ATGAAGTGGGTGACTTTTATTTCCCTTCTCTTTCTCT
porcine			TCAGCTCTGCTTATTCCAGGAATCTGCAAAGATTTG
albumin			CTCGTGATGCAGAGCACAAGAGTGAAATTGCCCAT
signal			CGCTACAATGATTTGAAAGAAGAAACATTTAAGGC
peptide			AGTTGCCATGATCACATTTGCCCAGTATCTCCAGAG
			GTGCTCTTATGAAGGACTGTCTAAGCTTGTGAAGG
			ATGTTGTTGATCTGGCACAAAAATGTGTAGCCAAT
			GAAGATGCTCCTGAATGCTCAAAACCACTGCCTTC
			CATTATCCTGGATGAAATCTGCCAAGTGGAAAAGC
			TCCGTGACTCTTATGGTGCAATGGCCGACTGCTGTA
			GCAAAGCTGATCCTGAAAGAAATGAGTGTTTCCTG
			TCATTTAAAGTTTCCCAACCAGACTTCGTTCAGCCA
			TACCAAAGACCAGCTTCTGATGTGATATGCCAGGA
			ATACCAGGACAACAGAGTGTCATTTCTGGGACATT
			TCATCTATTCTGTTGCAAGAAGACACCCCTTCTTGT
			ATGCCCCTGCAATCCTTAGTTTTGCTGTTGATTTTG
			AACATGCACTTCAAAGCTGTTGCAAAGAGAGTGAT
			GTCGGTGCTTGCCTGGACACCAAGGAAATTGTTAT
			GAGAGAAAAAGCCAAGGGAGTAAGTGTGAAGCAG
			CAGTATTTTTGTGGAATCTTGAAGCAGTTCGGAGAT
			AGAGTTTTCCAAGCACGACAACTTATTTACCTAAG
			CCAAAAATACCCCAAGGCTCCATTCTCAGAGGTTT
			CTAAATTTGTACATGATTCTATCGGCGTCCACAAAG
			AGTGCTGTGAAGGGGACATGGTGGAGTGCATGGAT
			GACATGGCACGTATGATGAGCAATCTGTGCTCTCA
			ACAAGATGTTTTCTCAGGTAAAATCAAAGACTGCT
			GTGAGAAGCCTATTGTGGAACGAAGCCAGTGCATT
			ATGGAGGCAGAATTTGATGAGAAACCTGCAGATCT
			TCCTTCATTAGTTGAAAAGTACATAGAAGATAAGG
			AAGTGTGTAAAAGTTTTGAAGCAGGCCACGATGCA
			TTCATGGCAGAGTTCGTTTATGAATACTCACGAAG
			ACACCCTGAGTTCTCCATACAGCTTATTATGAGAAT
			TGCCAAAGGATATGAATCACTTCTGGAAAAGTGCT
			GCAAAACTGATAACCCTGCTGAGTGCTACGCAAAT
			GCTCAAGAGCAACTGAACCAACATATCAAAGAAAC
			TCAGGATGTTGTGAAGACAAACTGTGATCTTCTCC
			ATGACCATGGCGAGGCAGACTTCCTCAAGTCCATC
			CTGATCCGCTACACTAAGAAAATGCCTCAAGTACC
			AACTGATCTCCTGCTTGAAACTGGAAAGAAAATGA
			CAACTATTGGTACTAAGTGCTGCCAGCTTCCTGAA
			GACAGACGCATGGCTTGTTCTGAGGGTTATCTGAG
			CATTGTGATTCATGATACGTGCAGGAAACAGGAGA
			CCACACCTATAAATGACAACGTTTCACAATGCTGC
			AGCAGCTCCTATGCTAACAGAAGACCATGTTTCAC
			TGCTATGGGAGTAGATACCAAATATGTTCCTCCAC
			CATTTAATCCTGATATGTTCAGCTTTGATGAAAAAT
			TGTGCAGTGCTCCTGCTGAAGAACGAGAAGTAGGC
			CAGATGAAATTGCTAATCAACCTCATTAAACGCAA
			GCCCCAGATGACAGAAGAACAAATAAAGACAATT
			GCTGATGGTTTCACTGCCATGGTTGACAAGTGCTGC
			AAGCAGTCGGACATCAATACATGCTTTGGAGAAGA
			GGGTGCCAACCTAATAGTCCAAAGCAGAGCCACAT
			TAGGAATTGGTGCTTAA (SEQ ID NO: 8)
Wild	porcine	NM_001005208	ATGAAGTGGGTGACTTTTATTTCCCTTCTCTTTCTCT
Type			TCAGCTCTGCTTATTCCAGGGGTGTGTTTCGTCGAG
Albumin			ATACATACAAGAGTGAAATTGCTCATCGGTTTAAA
			GATTTGGGAGAACAATATTTCAAAGGCCTAGTGCT
			GATTGCCTTTTCTCAGCATCTCCAGCAATGCCCATA
			TGAAGAGCATGTGAAATTAGTGAGGGAAGTAACTG
			AGTTTGCAAAAACATGTGTTGCTGATGAGTCAGCT
			GAAAATTGTGACAAGTCAATTCACACTCTCTTTGG
			AGATAAATTATGTGCAATTCCATCCCTTCGTGAACA
			CTATGGTGACTTGGCTGACTGCTGTGAAAAAGAAG
			AGCCTGAGAGAAACGAATGCTTCCTCCAACACAAA
			AATGATAACCCCGACATCCCTAAATTGAAACCAGA
			CCCTGTTGCTTTATGCGCTGACTTCCAGGAAGATGA
			ACAGAAGTTTTGGGGAAAATACCTATATGAAATTG
			CCAGAAGACATCCCTATTTCTACGCCCCAGAACTC
			CTTTATTATGCCATTATATATAAAGATGTTTTTTCA
			GAATGCTGCCAAGCTGCTGATAAAGCTGCCTGCCT
			GTTACCAAAGATTGAGCATCTGAGAGAAAAAGTAC
			TGACTTCCGCCGCCAAACAGAGACTTAAGTGTGCC
			AGTATCCAAAAATTCGGAGAGAGAGCTTTCAAAGC
			ATGGTCATTAGCTCGCCTGAGCCAGAGATTTCCCA
			AGGCTGACTTTACAGAGATTTCCAAGATAGTGACA
			GATCTTGCAAAAGTCCACAAGGAATGCTGCCATGG
			TGACCTGCTTGAATGTGCAGATGACAGGGCGGATC
			TTGCCAAATATATATGTGAAAATCAAGACACAATC
			TCCACTAAACTGAAGGAATGCTGTGATAAGCCTCT
			GTTGGAAAAATCCCACTGCATTGCTGAGGCAAAAA
			GAGATGAATTGCCTGCAGACCTGAACCCATTAGAA
			CATGATTTTGTTGAAGATAAGGAAGTTTGTAAAAA
			CTATAAAGAAGCAAAGCATGTCTTCCTGGGCACGT
			TTTTGTATGAGTATTCAAGAAGGCACCCAGACTAC
			TCTGTCTCATTGCTGCTGAGAATTGCCAAGATATAT
			GAAGCCACACTGGAGGACTGCTGTGCCAAAGAGG
			ATCCTCCGGCATGCTATGCCACAGTGTTTGATAAAT
			TTCAGCCTCTTGTGGATGAGCCTAAGAATTTAATCA
			AACAAAACTGTGAACTTTTTGAAAAACTTGGAGAG
			TATGGATTCCAAAATGCGCTCATAGTTCGTTACACC
			AAGAAAGTACCCCAAGTGTCAACTCCAACTCTTGT
			GGAGGTCGCAAGAAAACTAGGACTAGTGGGCTCTA
			GGTGTTGTAAGCGTCCTGAAGAAGAAAGACTGTCC
			TGTGCTGAAGACTATCTGTCCCTGGTCCTGAACCGG
			TTGTGCGTGTTGCACGAGAAGACACCAGTGAGCGA
			AAAAGTTACCAAATGCTGCACAGAGTCCTTGGTGA
			ACAGACGGCCTTGCTTTTCTGCTCTGACACCAGACG
			AAACATACAAACCCAAAGAATTTGTTGAGGGAACC
			TTCACCTTCCATGCAGACCTATGCACACTTCCTGAG
			GATGAGAAACAAATCAAGAAGCAAACTGCACTCGT
			TGAGTTGTTGAAACACAAGCCTCATGCAACAGAGG
			AACAACTGAGAACTGTCCTGGGCAACTTTGCAGCC
			TTTGTACAAAAGTGCTGCGCCGCTCCTGACCATGA
			GGCCTGCTTTGCTGTGGAGGGTCCGAAATTTGTTAT
			TGAAATTCGAGGGATCTTAGCCTAA (SEQ ID NO: 9)
Wild	chicken	NM_205261	ATGAAGTGGGTAACATTAATTTCATTCATTTTCCTC
Type			TTCAGTTCAGCAACATCCAGGAATCTGCAAAGATT
Albumin			TGCTCGTGATGCAGAGCACAAGAGTGAAATTGCCC
			ATCGCTACAATGATTTGAAAGAAGAAACATTTAAG
			GCAGTTGCCATGATCACATTTGCCCAGTATCTCCAG
			AGGTGCTCTTATGAAGGACTGTCTAAGCTTGTGAA
			GGATGTTGTTGATCTGGCACAAAAATGTGTAGCCA
			ATGAAGATGCTCCTGAATGCTCAAAACCACTGCCT
			TCCATTATCCTGGATGAAATCTGCCAAGTGGAAAA
			GCTCCGTGACTCTTATGGTGCAATGGCCGACTGCTG
			TAGCAAAGCTGATCCTGAAAGAAATGAGTGTTTCC
			TGTCATTTAAAGTTTCCCAACCAGACTTCGTTCAGC
			CATACCAAAGACCAGCTTCTGATGTGATATGCCAG
			GAATACCAGGACAACAGAGTGTCATTTCTGGGACA
			TTTCATCTATTCTGTTGCAAGAAGACACCCCTTCTT
			GTATGCCCCTGCAATCCTTAGTTTTGCTGTTGATTT
			TGAACATGCACTTCAAAGCTGTTGCAAAGAGAGTG
			ATGTCGGTGCTTGCCTGGACACCAAGGAAATTGTT
			ATGAGAGAAAAAGCCAAGGGAGTAAGTGTGAAGC
			AGCAGTATTTTTGTGGAATCTTGAAGCAGTTCGGA
			GATAGAGTTTTCCAAGCACGACAACTTATTTACCTA
			AGCCAAAAATACCCCAAGGCTCCATTCTCAGAGGT
			TTCTAAATTTGTACATGATTCTATCGGCGTCCACAA
			AGAGTGCTGTGAAGGGGACATGGTGGAGTGCATGG
			ATGACATGGCACGTATGATGAGCAATCTGTGCTCT
			CAACAAGATGTTTTCTCAGGTAAAATCAAAGACTG
			CTGTGAGAAGCCTATTGTGGAACGAAGCCAGTGCA
			TTATGGAGGCAGAATTTGATGAGAAACCTGCAGAT
			CTTCCTTCATTAGTTGAAAAGTACATAGAAGATAA
			GGAAGTGTGTAAAAGTTTTGAAGCAGGCCACGATG
			CATTCATGGCAGAGTTCGTTTATGAATACTCACGA
			AGACACCCTGAGTTCTCCATACAGCTTATTATGAG
			AATTGCCAAAGGATATGAATCACTTCTGGAAAAGT
			GCTGCAAAACTGATAACCCTGCTGAGTGCTACGCA
			AATGCTCAAGAGCAACTGAACCAACATATCAAAGA
			AACTCAGGATGTTGTGAAGACAAACTGTGATCTTC
			TCCATGACCATGGCGAGGCAGACTTCCTCAAGTCC
			ATCCTGATCCGCTACACTAAGAAAATGCCTCAAGT
			ACCAACTGATCTCCTGCTTGAAACTGGAAAGAAAA
			TGACAACTATTGGTACTAAGTGCTGCCAGCTTCCTG
			AAGACAGACGCATGGCTTGTTCTGAGGGTTATCTG
			AGCATTGTGATTCATGATACGTGCAGGAAACAGGA
			GACCACACCTATAAATGACAACGTTTCACAATGCT
			GCAGCAGCTCCTATGCTAACAGAAGACCATGTTTC
			ACTGCTATGGGAGTAGATACCAAATATGTTCCTCC
			ACCATTTAATCCTGATATGTTCAGCTTTGATGAAAA
			ATTGTGCAGTGCTCCTGCTGAAGAACGAGAAGTAG
			GCCAGATGAAATTGCTAATCAACCTCATTAAACGC
			AAGCCCCAGATGACAGAAGAACAAATAAAGACAA
			TTGCTGATGGTTTCACTGCCATGGTTGACAAGTGCT
			GCAAGCAGTCGGACATCAATACATGCTTTGGAGAA
			GAGGGTGCCAACCTAATAGTCCAAAGCAGAGCCAC
			ATTAGGAATTGGTGCTTAA (SEQ ID NO: 10)
Wild	Bovine	NM_180992	ATGAAGTGGGTGACTTTTATTTCTCTTCTCCTTCTCT
Type			TCAGCTCTGCTTATTCCAGGGGTGTGTTTCGTCGAG
Albumin			ATACACACAAGAGTGAGATTGCTCATCGGTTTAAA
			GATTTGGGAGAAGAACATTTTAAAGGCCTGGTACT
			GATTGCCTTTTCTCAGTATCTCCAGCAGTGTCCATT
			TGATGAGCATGTAAAATTAGTGAACGAACTAACTG
			AGTTTGCAAAAACATGTGTTGCTGATGAGTCCCAT
			GCCGGCTGTGAGAAGTCACTTCACACTCTCTTTGGA
			GATGAATTGTGTAAAGTTGCATCCCTTCGTGAAAC
			CTATGGTGACATGGCTGACTGCTGTGAGAAACAAG
			AACCTGAGAGAAATGAATGCTTCTTGTCACACAAA
			GATGATAGCCCTGATCTACCTAAACTCAAACCTGA
			CCCCAATACTTTGTGTGACGAGTTTAAGGCCGATG
			AAAAGAAGTTTTGGGGAAAATACCTATACGAAATT
			GCTAGAAGACATCCCTACTTTTATGCACCAGAACT
			CCTTTACTATGCTAATAAATATAATGGAGTTTTTCA
			AGAATGCTGCCAAGCTGAAGATAAAGGTGCCTGCC
			TGCTACCAAAGATTGAAACTATGAGGGAAAAGGTA
			CTGACTTCATCTGCCAGACAGAGACTCAGGTGTGC
			CAGTATTCAAAAATTTGGAGAAAGAGCTTTAAAAG
			CATGGTCAGTAGCTCGCCTGAGCCAGAAATTTCCC
			AAGGCTGAGTTTGTAGAAGTTACCAAGCTAGTGAC
			AGATCTCACAAAAGTGCACAAGGAATGCTGCCATG
			GAGACCTACTTGAATGCGCAGATGACAGGGCGGAC
			CTTGCCAAGTACATATGTGATAATCAAGATACAAT
			CTCCAGTAAACTGAAGGAATGCTGTGATAAGCCTT
			TGTTGGAAAAATCCCACTGCATTGCTGAGGTAGAA
			AAAGATGCCATACCTGAAAACTTGCCCCCATTAAC
			TGCTGACTTTGCTGAAGATAAGGATGTATGCAAAA
			ACTATCAAGAAGCAAAGGATGCCTTCCTGGGCTCA
			TTTCTTTATGAATATTCAAGAAGGCATCCTGAATAT
			GCTGTCTCAGTGCTATTGAGACTTGCCAAGGAATA
			TGAAGCCACACTGGAGGAATGCTGTGCCAAAGATG
			ATCCACATGCATGCTATTCCACAGTGTTTGACAAAC
			TTAAGCATCTTGTGGATGAGCCTCAGAATTTAATTA
			AACAAAACTGTGACCAATTCGAAAAACTTGGAGAG
			TATGGATTCCAAAATGCGCTCATAGTTCGTTACACC
			AGGAAAGTACCCCAAGTGTCAACTCCAACTCTCGT
			GGAGGTTTCAAGAAGCCTAGGAAAAGTGGGTACTA
			GGTGTTGTACAAAACCGGAATCAGAAAGAATGCCC
			TGTACAGAAGACTATCTGAGCTTGATCCTGAACCG
			GTTGTGCGTGCTGCATGAGAAGACACCAGTGAGTG
			AAAAAGTCACCAAGTGCTGCACAGAGTCATTGGTG
			AACAGACGGCCATGTTTCTCTGCTCTGACACCTGAT
			GAAACATATGTACCCAAAGCCTTTGATGAGAAATT
			GTTCACCTTCCATGCAGATATATGCACACTTCCCGA
			TACTGAGAAACAAATCAAGAAACAAACTGCACTTG
			TTGAGCTGTTGAAACACAAGCCCAAGGCAACAGAG
			GAACAACTGAAAACCGTCATGGAGAATTTTGTGGC
			TTTTGTAGACAAGTGCTGCGCAGCTGATGACAAAG
			AAGCCTGCTTTGCTGTGGAGGGTCCAAAACTTGTT
			GTTTCAACTCAAACAGCCTTAGCCTAA (SEQ ID NO:
			11)
TERT	chicken	Modified	ATGGAGCGCGGGGCTCAGCCGGGAGTCGGTGTGCG
		NM_001031007.1	GCGGCTCCGCAATGTAGCGCGGGAGGAGCCCTTCG
		(substitution	CCGCGGTCCTGGGCGCGCTGCGGGGCTGCTACGCC
		made at	GAGGCCACGCCGCTGGAGGCCTTCGTCCGGCGGCT
		position 2667	GCAGGAGGGTGGCACCGGGGAGGTCGAGGTGCTG
		T to C)	CGAGGCGACGACGCTCAGTGCTACCGGACCTTCGT
			GTCGCAGTGCGTGGTGTGCGTCCCCCGCGGTGCTC
			GCGCCATCCCCCGGCCCATCTGCTTCCAGCAGTTAT
			CCAGTCAGAGCGAAGTCATCACAAGAATCGTTCAG
			AGGCTGTGTGAAAAGAAAAAGAAGAACATCCTTGC
			GTATGGATACTCCTTGCTGGATGAGAACAGTTGTC
			ACTTCAGAGTTTTGCCATCTTCGTGTATATACAGCT
			ATCTGTCCAATACTGTAACAGAAACGATTCGCATC
			AGTGGCCTCTGGGAGATACTGCTGAGTAGGATAGG
			GGACGACGTGATGATGTACCTGCTGGAGCACTGTG
			CACTCTTCATGCTGGTTCCCCCAAGTAACTGTTACC
			AGGTCTGCGGGCAACCAATTTATGAACTTATTTCGC
			GTAACGTAGGGCCATCCCCAGGGTTTGTTAGACGA
			CGGTACTCAAGGTTTAAACATAATAGCTTGCTTGA
			CTATGTGCGAAAAAGGCTTGTGTTTCACAGGCACT
			ATCTTTCCAAGTCGCAGTGGTGGAAGTGCAGGCCG
			AGACGTCGAGGTCGTGTCTCCAGCAGGAGAAAAAG
			AAGGAGCCATAGGATACAAAGCCTAAGGTCTGGTT
			ATCAGCCTTCTGCAAAAGTGAACTTTCAAGCAGGT
			AGGCAGATCAGCACAGTTACTGCACGTCTGGAAAA
			ACAGAGCTGCTCCAGTTTATGTTTGCCAGCTAGAG
			CACCATCTTTAAAAAGGAAGCGTGATGGAGAACAG
			GTTGAAATCACAGCTAAGAGAGTGAAAATAATGGA
			GAAAGAGATAGAGGAACAGGCTTGTAGTATCGTTC
			CTGATGTAAACCAAAGTAGCTCCCAGAGGCATGGA
			ACCTCCTGGCATGTAGCACCACGTGCTGTAGGTCTT
			ATTAAAGAACATTACATTTCTGAAAGAAGTAACAG
			TGAGATGTCTGGTCCTTCTGTAGTTCACAGATCTCA
			CCCTGGGAAGAGGCCTGTGGCAGACAAAAGCTCTT
			TTCCACAAGGAGTTCAGGGTAACAAACGCATAAAG
			ACCGGTGCAGAAAAACGAGCAGAATCCAATAGAA
			GGGGCATAGAGATGTATATAAACCCAATCCATAAA
			CCCAATAGAAGGGGCATAGAGAGGCGTATAAATCC
			AACCCACAAACCTGAGTTGAATTCTGTACAAACTG
			AACCAATGGAAGGTGCTTCTTCAGGGGACAGAAAG
			CAGGAAAATCCCCCAGCTCATTTGGCAAAGCAGTT
			ACCAAATACATTGTCGCGCTCTACAGTGTACTTTGA
			GAAGAAATTTCTTCTGTATTCCCGCAGTTACCAAGA
			ATATTTTCCTAAATCGTTCATACTGAGCCGCCTGCA
			GGGTTGTCAGGCAGGTGGAAGGCGGCTTATAGAAA
			CTATATTCTTAAGCCAAAACCCATTAAAGGAACAG
			CAGAACCAAAGCCTACCACAGCAAAAGTGGCGAA
			AGAAGAGGTTGCCCAAACGCTACTGGCAAATGAGA
			GAGATATTTCAGAAGCTGGTAAAGAACCATGAGAA
			GTGCCCTTATTTAGTTTTCTTGAGGAAAAATTGCCC
			TGTTTTGCTTTCTGAAGCATGTTTGAAAAAGACGGA
			GCTGACCTTGCAGGCGGCTCTGCCTGGGGAAGCAA
			AGGTTCACAAGCACACAGAACATGGGAAAGAGTC
			CACTGAGGGTACTGCACCGAACAGCTTCCTCGCTC
			CTCCCTCAGTGCTAGCATGTGGGCAGCCAGAGAGA
			GGGGAACAGCACCCTGCAGAGGGGAGTGATCCGCT
			CCTCAGGGAGCTGCTCAGGCAGCACAGCAGCCACT
			GGCAGGTGTATGGCTTTGTGAGGGAGTGCCTGGAG
			CGGGTGATCCCTGCTGAGCTGTGGGGTTCAAGCCA
			TAACAAATGCCGGTTCTTTAAAAACGTGAAAGCAT
			TCATTTCCATGGGGAAGTATGCTAAGCTTTCATTGC
			AGCAGCTGATGTGGAAGATGAGAGTGAATGACTGC
			GTATGGCTTCGTCTGGCCAAAGGTAATCACTCTGTT
			CCTGCCTATGAACATTGTTACCGTGAAGAAATTCTG
			GCAAAATTCCTATACTGGCTGATGGATTCCTATGTT
			ATCGAGTTGCTCAAATCATTTTTCTATATCACCGAG
			ACCATGTTCCAGAAAAACATGCTTTTCTACTACCGA
			AAGTTTATCTGGGGCAAGTTACAGAACATTGGAAT
			TAGAGACCATTTTGCCAAAGTACATCTACGTGCCTT
			GTCTTCAGAGGAGATGGAAGTGATCCGTCAAAAAA
			AGTATTTTCCTATTGCATCAAGGCTCCGGTTCATTC
			CTAAAATGAATGGTTTAAGACCCGTAGTAAGACTA
			AGCCGTGTTGTTGAAGGACAGAAACTCAGCAAGGA
			AAGCAGAGAAAAGAAGATACAGCGCTATAACACT
			CAGCTAAAAAATCTATTTAGTGTTTTAAACTATGAA
			CGAACTGTAAACACCAGTATCATTGGCTCCTCAGT
			ATTCGGGAGAGATGATATCTACAGGAAGTGGAAGG
			AGTTTGTTACAAAGGTTTTTGAATCAGGTGGTGAA
			ATGCCTCATTTCTACTTTGTAAAGGGTGATGTATCC
			AGAGCTTTTGATACCATTCCTCACAAGAAACTTGTG
			GAAGTGATATCACAGGTCTTGAAACCTGAGAGCCA
			AACTGTCTATGGAATAAGGTGGTATGCAGTGATTA
			TGATTACCCCAACTGGAAAAGCCAGGAAACTCTAT
			AAGAGACATGTTTCTACTTTCGAGGATTTTATTCCA
			GACATGAAGCAGTTTGTGTCCAAGCTTCAAGAGAG
			AACTTCATTACGAAATGCAATAGTAGTTGAACAGT
			GCTTAACTTTTAATGAGAACAGTTCCACCCTGTTTA
			CTTTCTTTCTTCAAATGTTACATAATAACATCCTGG
			AGATTGGGCACAGGTACTATATACAGTGCTCTGGA
			ATCCCACAGGGCTCCATTTTGTCAACCTTACTTTGC
			AGCTTATGCTACGGAGACATGGAAAACAAATTACT
			CTGTGGGATCCAGAAGGATGGAGTCCTAATACGTC
			TTATTGATGACTTTTTGCTGGTTACGCCACATTTAA
			TGCAGGCAAGAACTTTTCTAAGGACTATAGCAGCA
			GGTATTCCTGAGTATGGCTTTTTAATAAATGCCAAG
			AAGACTGTGGTGAATTTTCCTGTTGATGATATCCCG
			GGATGTTCCAAGTTCAAACATCTGCCAGATTGTCGT
			TTGATCTCATGGTGTGGTTTATTATTGGATGTGCAG
			ACACTTGAGGTTTATTGTGATTACTCCAGTTATGCC
			TTTACTTCTATCAGATCAAGTCTTTCCTTCAATTCA
			AGTAGAATAGCTGGGAAAAACATGAAATGCAAATT
			GACTGCAGTCCTCAAACTGAAATGCCATCCTTTACT
			TCTTGACTTAAAGATCAACAGCCTTCAGACAGTTCT
			AATTAACATCTACAAGATATTTTTACTTCAGGCTTA
			CAGGTTCCATGCCTGTGTTCTTCAGCTTCCATTCAA
			CCAGAAAGTTAGGAATAATCCTGATTTCTTCCTAA
			GGATCATCTCTGATACTGCTTCATGCTGCTATTTTA
			TCCTGAAAGCTAAAAATCCAGGAGTTTCTTTAGGT
			AGCAAAGATGCATCTGGCATGTTCCCTTTTGAGGC
			AGCAGAATGGCTGTGCTACCATGCCTTCATTGTCA
			AACTGTCCAACCACAAAGTTATTTACAAATGCTTA
			CTTAAGCCCCTTAAAGTCTATAAGATGCATCTGTTT
			GGGAAGATCCCAAGGGATACTATGGAACTGCTGAA
			GACGGTGACGGAACCATCGCTTTGTCAAGATTTCA
			AAACTATACTGGACTAA (SEQ ID NO: 12)
cMyoDER	chicken		ATGGACTTACTGGGCCCCATGGAAATGACGGAGGG
			CTCCCTCTGCTCCTTCACGGCCGCCGATGACTTCTA
			TGACGACCCGTGCTTCAACACGTCGGACATGCACT
			TCTTCGAGGACCTGGACCCCCGGCTGGTGCACGTG
			GGCGGGCTGCTGAAGCCCGAGGAGCACCCGCACCA
			CCACGGGCACCACCACGGGAACCCACACGAGGAG
			GAGCACGTGCGGGCGCCCAGTGGGCACCACCAGGC
			CGGCCGCTGCCTGCTGTGGGCGTGCAAGGCCTGCA
			AGAGGAAGACCACCAACGCTGACCGCCGCAAAGC
			CGCCACCATGAGGGAACGGCGGCGGCTCAGCAAG
			GTCAACGAGGCCTTCGAGACCCTCAAGCGCTGCAC
			TTCCACCAACCCCAACCAGCGCCTGCCCAAGGTGG
			AGATCCTGCGCAACGCCATCCGCTACATCGAGAGC
			CTGCAGGCCCTGCTGCGTGAGCAGGAGGGCGATTC
			TTCTACAGAGCTGCGAGCTCCAACCCTTTGGACAA
			GTCCACTGGTGGTTAAACATAACAAGAAGAACAGT
			CCGGCTCTGTCTCTGACAGCAGAACAGATGGTCAG
			TGCCTTGCTGGAAGCTGAGCCACCTATAGTTTATTC
			TGAATATGACCCCAATAGACCATTCAACGAAGCAT
			CTATGATGACCCTGTTGACCAACCTTGCAGACAGA
			GAATTAGTGCACATGATCAACTGGGCAAAGAGAGT
			TCCAGGATTTGTGGATTTAACACTCCATGATCAGGT
			CCATCTGCTGGAATGTGCCTGGTTAGAGATATTGAT
			GATCGGCTTAGTCTGGCGCTCCATGGAACACCCAG
			GAAAGCTTTTATTTGCACCTAATCTATTACTGGACA
			GGAATCAAGGGAAATGTGTAGAGGGCATGGTGGA
			AATCTTTGACATGCTACTGGCTACTGCTGCTCGGTT
			TCGGATGATGAACCTTCAAGGGGAGGAATTTGTGT
			GCCTTAAGTCCATCATCCTGCTCAATTCTGGTGTGT
			ACACTTTTCTTTCTAGCACCTTGAAATCTCTGGAAG
			AGAGGGACTATATCCACCGTGTTCTGGACAAAATC
			ACAGATACTCTGATACACCTAATGGCAAAGTCAGG
			TCTTTCTCTGCAGCAGCAACACCGGCGACTAGCTC
			AGCTCCTCCTTATCCTCTCTCACATCAGGCATATGA
			GCAACAAAGGAATGGAGCACCTGTACAATATGAA
			GTGTAAAAATGTAGTTCCGCTCTACGACCTCTTACT
			GGAGATGCTGGACGCTCACCGCCTACATGCACCGG
			CAGCCAGGAGTGCTGCACCAATGGAAGAGGAGAA
			CCGAAACCAACTGACAACCGCACCAGCTTCATCTC
			ATTCCCTGCAGTCCTTTTACATTAACAGCAAAGAA
			GAGGAGAGTATGCAGAATACAGCTATCGCCGATGC
			ATACTACCCAGTGCTGGAGCACTACAGCGGGGAGT
			CAGATGCCTCCAGCCCTCGCTCCAACTGCTCCGAC
			GGCATGATGGAGTACAGCGGGCCGCCCTGTAGCTC
			TCGCAGGAGAAACAGCTACGACAGCAGCTACTACA
			CGGAATCACCAAATGACCCAAAGCATGGGAAGAG
			TTCTGTTGTTTCCAGCCTCGACTGCCTCTCAAGCAT
			TGTGGAGAGGATTTCCACAGACAACTCCACATGTC
			CCATACTGCCTCCAGCTGAAGCTGTAGCTGAAGGG
			AGTCCCTGTTCCCCCCAGGAAGGAGCAAACCTGAG
			TGACAGTGGAGCCCAGATTCCTTCCCCCACCAACT
			GCACCCCTCTTCCCCAGGAAAGCAGCAGCAGCAGC
			AGCAGCAATCCAATCTACCAAGTGCTATAA (SEQ
			ID NO: 13)
IGF2	Cow	NM_174087.3	ATGGGGATCACAGCAGGAAAGTCGGTGCTGGTGCT
	[Bos		TCTTGCCTTCTTGGCCTTCGCCTCGTGCTGCTATGCT
	Taurus]		GCTTACCGCCCCAGCGAGACTCTGTGCGGCGGGGA
			GCTGGTGGACACCCTCCAGTTTGTCTGTGGGGACC
			GCGGCTTCTACTTCAGCCGACCATCCAGCCGCATA
			AACCGACGCAGCCGTGGCATCGTGGAAGAGTGTTG
			CTTCCGAAGCTGCGACCTGGCCCTGCTGGAGACTT
			ACTGTGCCACCCCCGCCAAGTCCGAGAGGGATGTG
			TCTGCCTCTACGACCGTGCTTCCGGACGACGTCACC
			GCATACCCCGTGGGCAAGTTCTTCCAATATGACAT
			CTGGAAGCAGTCCACCCAGCGCCTGCGCAGGGGCC
			TGCCCGCCTTCCTGCGAGCACGCCGGGGTCGCACG
			CTCGCCAAGGAGCTGGAGGCGCTCAGAGAGGCCA
			AGAGTCACCGTCCGCTGATCGCCCTGCCCACCCAG
			GACCCTGCCACCCACGGGGGCGCCTCTTCCAAGGC
			ATCCAGCGATTAG (SEQ ID NO: 15)
IGF1	Zebrafish	NM_131825.2	ATGTCTAGCGGTCATTTCTTCCAGGGGCATTGGTGT
	[Danio		GATGTCTTTAAGTGTACCATGCGCTGTCTCCCGAGT
	rerio]		ACCCACACCCTCTCACTGGTGCTGTGCGTCCTCGCG
			TTGACTCCCGCGACTCTGGAGGCGGGGCCGGAGAC
			GCTGTGCGGGGCGGAGCTTGTAGACACGCTGCAGT
			TTGTGTGTGGAGACAGGGGCTTTTATTTCAGCAAA
			CCGACAGGATATGGACCTAGTTCAAGAAGGTCACA
			CAACCGTGGCATCGTGGACGAATGCTGCTTTCAGA
			GCTGTGAGCTACGGCGCCTCGAGATGTATTGTGCG
			CCTGTGAAGACAGGCAAATCTCCACGATCTCTACG
			AGCACAACGACACACAGATATTCCCAGGACACCAA
			AGAAACCTATATCTGGGCATAGCCACTCTTCCTGTA
			AGGAGGTTCATCAGAAGAACTCGAGCCGAGGAAA
			CACAGGGGGCAGAAACTATCGCATGTAG (SEQ ID
			NO: 16)
serum	Rainbow	XM_021614654.1	ATGAGGAGACCCTGTATCCTGGCCATCCAGCCTGA
albumin	trout		CACGGAGTTCATGCCCCCAGAGCTGGATGCCAGCA
1	[Oncorhynchus		ACTTCCACATGGGCCCTGAGCTCTGCACCAAGGAC
	mykiss]		AGCAAGGAGCTGCTGCTCTCTGGGAAGAAACTACT
			GTATGGTGTGGTCAGACATAAGACCACCATCACTG
			AGGAGCAGCTGAAGTCCATCTCTACTAAATATCAC
			AGTATGAAGGAGAAGTGCTGTGCTGCTGAGGACCA
			AGCAGCATGCTTCACTGAGGAGGCACCCAAGCTGG
			TTGCTGAGAGTGCAGAGCTGGTCAAGGCTTAA
			(SEQ ID NO: 17)
GLUL	Tilapia	NM_001279668.1	ATGGCTACATCCGCCAGCGCCAGCTTGAGTAAAGC
	[Oreochromis		TGTCAAGCAGCAGTACATGGAGCTCCCTCAGGGGG
	niloticus]		ACAAAGTCCAGGCCATGTACATCTGGATCGACGGA
			ACCGGAGAGGGGCTCCGATGCAAAACCAGGACGC
			TTGATTCTGAGCCCAAAAGCATCGAAGATCTTCCT
			GAATGGAACTTTGACGGATCCAGTACCTACCAGTC
			CGAAGGCTCCAACAGCGACATGTATCTGATCCCCT
			CAGCCATGTTCCGCGATCCATTCCGCAAAGACCCC
			AACAAGCTGGTGCTGTGTGAAGTCCTGAAGTACAA
			CCGTAAACCTACAGAAACCAACCTTCGGCTCACCT
			GTAAGAAAGTGATGGATATGGTGGCGGATCAGCAT
			CCTTGGTTTGGCATGGAGCAGGAGTACACCATCCT
			TGGAACGGACGGGCATCCATTTGGCTGGCCATCTA
			ATGGTTTCCCCGGACCACAGGGGCCGTACTACTGT
			GGTGTTGGAGCTGACAAAGCCTATGGCAGGGACGT
			AGTCGAGGCCCATTACAAAGCTTGTTTGTACGCTG
			GAGTCCAGATTTGTGGCACAAATGCTGAAGTAATG
			CCTGCTCAGTGGGAGTTCCAGGTCGGACCTTGCGA
			AGGCATTGACATGGGCGATCATTTGTGGGTAGCGC
			GCTTCATCCTGCACCGTGTCTGTGAGGATTTTGGCG
			TCGTCGCCTCATTTGATCCCAAGCCAATCCCTGGAA
			ACTGGAACGGTGCTGGCTGCCATACAAACTTCAGC
			ACGAAAGAGATGAGGGAAGACGGTGGATTGAAAG
			CTATTGAGGATTCCATTGAGAAGCTTGGAAAGAGG
			CACAGCTACCACATTCGTGCCTACGACCCCAAAGG
			GGGGCTCGACAACGCCCGCCGTCTCACTGGCCGCC
			ATGAAACCTCAAACATCAACGAATTCTCTGCTGGT
			GTGGCCAACCGTGGTGCCAGCATTCGCATTCCTCGT
			AATGTTGGTCAGGAGAAGAAAGGCTACTTCGAAGA
			CCGTCGCCCTTCAGCCAACTGTGACCCGTACAGTGT
			GACCGAGGCCCTGATCCGCACCTGTCTGCTGAACG
			AGGAAGGAGATGAACCCGCGGATTACTAA (SEQ ID
			NO: 18)
IGF2	Rainbow	NM_001124697.1	ATGGAAACCCAGAAAAGACACGAATACCACTCAGT
	trout		TTGTCACACCTGCCGGAGAACGGAAAACACAAGAA
	[Oncorhynchus		TGAAGGTCAAGATGATGTCTTCGTCAAATCGAGTG
	mykiss]		CTGGTCATTGCGCTGGCACTTACTCTGTACATTGTT
			GAAGTGGCTTCGGCAGAAACGCTATGTGGAGGAGA
			ACTGGTGGACGCGCTGCAGTTCGTCTGTGAAGATA
			GAGGATTCTATTTCAGTAGGCCAACCAGCAGGTCT
			AACAGCAGACGCTCCCAGAACCGTGGTATCGTGGA
			GGAGTGTTGTTTCCGTAGCTGTGACCTCAACCTGTT
			GGAGCAGTACTGTGCCAAACCTGCCAAGTCAGAGA
			GGGACGTGTCGGCCACCTCTCTACAGATCATTCCC
			ATGGTGCCCACAATCAAACAGGATGTCCCAAGAAA
			ACATGTGACTGTGAAGTATTCCAAATATGAGGCGT
			GGCAGAGGAAGGCTGCTCAGCGGCTCCGGAGGGG
			CGTCCCGGCCATCCTCAGGGCCCGGAAGTTCCGGA
			GGCAGGCGGTGAAGATCAAGGCCCAAGAGCAGGC
			GATGTTCCACCGGCCTCTGATCACCCTGCCCAGCA
			AGCTTCCCCCAGTCCTGCCCCCCACGGACAACTAC
			GTCAGCCACAATTGA (SEQ ID NO: 19)
IGF1	Tropical	XM_002936829.4	ATGGAAAAAAACAACAGTCTTTCAACACAATTATT
	clawed		TAAGTGCTACTTTTGTGATTTCTTAAAGCTGAAGAT
	frog		GCACAAAATGTCCTACATTCATCTGCTCTACCTGGC
	[Xenopus		TTTGTGTTTCCTGACTTTAACCCATTCAGCAGCTGC
	tropicalis]		TGGACCAGAGACCCTCTGTGGAGCCGAACTGGTAG
			ACACTCTTCAGTTTGTATGTGGAGACAGAGGCTTCT
			ATTTTAGCAAGCCAACAGGGTACGGATCCAGCAAT
			CGAAGATCGCATCACAGAGGAATAGTAGATGAGTG
			CTGTTTCCAAAGCTGTGATTTCAGAAGGCTGGAGA
			TGTACTGCGCTCCTGCCAAGCCAGCCAAATCAGCA
			CGTTCTGTACGTGCTCAACGTCACACTGACATGCCA
			AAAGCCCAGAAGGAAGTACACCTAAAGAATGCAA
			GTCGAGGAAACACAGGGAGTCGAGGATTCCGAAT
			GTAA (SEQ ID NO: 20)
GLUL	Tropical	XM_004914038.3	ATGGCAACCTCCGCCAGTGCTCAGTTGAGTAAGGC
	clawed		CATAAAGCAGATGTATCTGGAACTGCCACAGGGAG
	frog		ATAAGGTGCAGGCTATGTACATCTGGGTTGATGGG
	[Xenopus		ACCGGGGAGGGTCTTCGCTGCAAGACTCGCACTCT
	tropicalis]		GGACAGTGAACCCAAGACCATAGAAGATCTTCCTG
			AATGGAACTTCGATGGATCTAGCACATACCAATCC
			GAGGGTTCCAACAGTGACATGTACCTGATTCCAGT
			TGCAATGTTTAGAGACCCTTTTCGAAGGGACCCCA
			ACAAGCTGGTACTCTGCGAGGTGCTCAAATACAAC
			CGAAAAACAGCTGAAACAAACTTGCGTCATACATG
			TAACCAGATAATGGACATGATGGCCAATGAGCATC
			CATGGTTTGGCATGGAACAGGAATACACATTGCTG
			GGTATGGATGGACACCCTTTTGGCTGGCCTTCAAAT
			GGCTTCCCAGGACCACAAGGTCCCTATTACTGTGG
			AGTGGGTGCAGATAAGGCATATGGTCGGGATATTG
			TGGAGGCTCATTATCGGGCTTGCCTTTATGCTGGTG
			TGAAAATTGCAGGAACAAATGCAGAAGTTATGCCA
			GCACAGTGGGAGTTCCAAATTGGGCCATGTGAGGG
			AATAGAAATGGGAGATCACCTTTGGATTGCTCGAT
			TTATACTGCATAGAATTTGTGAGGATTTTGGGATCA
			TTGTTTCGTTTGACCCAAAGCCCATAACTGGAAACT
			GGAATGGAGCTGGATGTCACACCAATTTCAGCACA
			AAGTCAATGCGTGAAGAAGGAGGCCTTAAGGACAT
			AGAAGAATCCATTGAACGTCTAAGCAAACGTCATG
			ATTATCACATCAGAATGTATGACCCAAGGGGTGGT
			AAAGACAATGCCCGTCGTCTCACAGGTTTCCATGA
			GACCTCCAGCATCCATGAGTTCTCTGCAGGAGTGG
			CAAACCGTGGTGCCAGTATCCGCATTCCCCGCAGT
			GTAGGCCAGGAGAAGAAAGGCTATTTTGAAGATCG
			TCGTCCATCAGCCAACTGTGATCCCTATGCTGTGAC
			AGAAGCTATGATCAGAACCTGCCTACTGAATGAAA
			CTGGAGACGAACCTCTTGAATACAAGAACTAA
			(SEQ ID NO: 21)
ALB	Tropical	BC075287.1	ATGAACGCGTTGATGCGGCGTGCCTGCTGCGGGGC
	clawed		GCTATTCCCCCTCTCATTCCGACTGGCCGCGCTGAG
	frog		CCCTATGAAGGGAGCTAGTAACTTTAGCTGCGGTA
	[Xenopus		ACGTGTGCGCCTCTCCTGCCGGATGTTGGGCGCCA
	tropicalis]		CCAAGTGGACACGACACGGGGATAAAAGTGTACA
			ACAGCCTTACTAGGAGGAAGGATCCACTTATTCTG
			GCAGATCCGACAGTAGCGACATGGTATAGCTGTGG
			ACCTACAGTTTATGACCATGCACATCTTGGACATGC
			ATGTTCTTATGTTAGATTTGACATAATTCGAAGGAT
			TCTGCTCAAGGTTTTTGGGATTGATACAGTCGTGGT
			GATGGTAGTCACAGACATTGATGATAAGATAATCA
			AGAGAGCAAAGGAGCTCAATATATCTCCTGTGGCC
			TTAGCTCGTACTTACGAACAGGATTTTAAACAAGA
			CATGACTGCGTTGAAGGTCCTTCCACCAACAGTAT
			ACATGAGAGTTACTGAAAATATTCCACAGATCATA
			TCATTTATTGAACACATAATTGCCAATGGATATGCA
			TATGCTACCTCACAAGGAAATGTTTATTTTGATGTT
			CAGTCGATTGGAGAGCGATATGGGAAATTTAATGA
			TTCTTTCAGTGATACAGCCAGCGAATCAGCATCAC
			AAGATAAAAGGCATATCCGAGATTTTGCTTTGTGG
			AAAACATCCAAGCCTGAGGAGCCTTACTGGGCTTC
			TCCTTGGGGCAAGGGAAGACCTGGCTGGCACATAG
			AGTGTTCCACAATTGCAAGTTCTGTATTTGGCAAAC
			ATCTAGACATTCACACTGGTGGGATTGACCTTGCTT
			TCCCTCATCATGAAAATGAAATTGCTCAGTGTGAG
			GCATATCACCAGAGCACACAGTGGGGAAACTATTT
			CCTTCATACTGGACATTTACATTTGAAAGGGAATG
			AAGAAAAAATGTCAAAATCCCTGAGAAACTATCTG
			ACAGTTAAGGAGTTTTTAAAGTCCTTTTCCCCTGAC
			CAGTTTAGAATGTTTTGTCTGCGCTCAAAATATAAA
			TCAGCCGTGGAATACAGCAACGGGTCCATGCATGA
			TGCAGTAAATACCCTACACACCATCTCTTCGTTTGT
			CGATGATGCAAAAGCCTATATGAAAGGTCAGCTGA
			TTTGCCAACCAGTGCAGGAGGCTTTACTCTGGCAA
			AGGCTGAATGAAACAAAAGTAAATGTTAAGGCTGC
			GTTTTCAGATGACTTTGACACCCCACGAGCAGTTG
			ATGCAGTTATGGACCTCATTCACCATGGCAACAGA
			CAGCTTAAGGCTGTTTCCAAGGAGTCAAACTCTCC
			CAGGAGCTCTGTAGTTTATGGTGCCATGATCTCTTA
			CATTGAACAATTTCTGGAGATATTGGGAATTTCCTT
			GAGCCAAAACCAGGTCGCTGCAGAAGATAGACACT
			CGGCTGTTCTCTTTAATGTAGTAGAAGAAATGATC
			AGTTTTAGAAGTAAGGTGCGGAATTACGCCCTGGC
			TGCAGATGAATCACCAAATGCAATAGGACAAGAG
			GAAAAACAGCAATACAAGGAGAGGAGAAGGCAGT
			TGTTACTGGAAAGGGAACCACTCCTACAGGCTTGT
			GACATAATGCGCCAACATCTGGCTGTATATGGCAT
			AAATGTAAAGGATCGTGGAAATACATCAACATGGG
			AACTACTTGACCGCAAAGAAGAAACCTAG (SEQ ID
			NO: 22)
IGF2	Tropical	NM_001113672.1	ATGAGGCATCTCCTCCTCCTCTCTATCACCTTCCTG
	clawed		GTATACACGCTAGACTCTGCTAAAGCCTATGGAGC
	frog		AACGGAGACCCTGTGCGGTGGGGAGCTGGTGGACA
	[Xenopus		CCCTGCAGTTTGTTTGTGGAGACAGGGGCTTCTATT
	tropicalis]		TCAGCAGGAATAATGGCCGCTCCAACCGCAGGGCT
			AACAGGGGGATTGTGGAAGAATGTTGCTTCCGGAG
			CTGTGATTTGGAACTGTTGGAAACGTACTGCGCAA
			AGCCAGCTAAGAACGAGAGGGATGTCTCCACTGCA
			CCCTCCACAGCAATACCACCACTGAACAAGCAGGA
			CCTGTACCACAAACATCACCACACAAAGAGCTCCA
			AGTATGACATTTGGCAGAGGAAGTCTATCCATCGG
			CTGCGGAGAGGAGTCCCTGCCATTGTACGTGCTAG
			GCAGTATCGATTGCTAATGCAGCAGGCTGAAGAAT
			CAGAGCAGGCACTATCACATCGGCCCCTTACCACC
			TTACCCATAACGCGGCCTCTCCATCTGCAACAAAC
			CTCAGAACCTTCCCTCAATTGA (SEQ ID NO: 23)
GLUL	Chicken	NM_205493.1	ATGGCCACCTCGGCGAGCTCCCACCTGAGCAAAGC
	[Gallus		CATCAAGCACATGTACATGAAGCTGCCGCAGGGTG
	gallus]		AGAAGGTCCAAGCCATGTACATCTGGATCGACGGG
			ACTGGGGAGCACCTCCGCTGCAAAACCCGCACTCT
			GGACCACGAACCCAAGAGCCTGGAAGATCTCCCCG
			AGTGGAACTTTGATGGCTCCAGCACCTTCCAAGCC
			GAAGGCTCCAACAGCGACATGTACCTGCGACCTGC
			TGCCATGTTCCGGGACCCTTTTCGCAAGGATCCCAA
			CAAATTAGTTCTCTGTGAGGTCTTCAAATACAACCG
			CCAGTCTGCAGACACAAATCTTCGGCACACCTGTA
			GGCGGATTATGGATATGGTGTCCAACCAGCACCCC
			TGGTTTGGGATGGAGCAGGAGTACACCCTTCTGGG
			AACAGATGGTCATCCGTTTGGCTGGCCTTCCAATTG
			CTTCCCTGGACCCCAAGGTCCGTACTACTGCGGTGT
			AGGAGCTGACAAAGCCTATGGCAGAGACATTGTGG
			AGGCCCACTACCGAGCGTGCCTGTATGCTGGTGTG
			AAAATTGGAGGAACCAACGCAGAAGTGATGCCAG
			CCCAGTGGGAGTTCCAGGTGGGACCGTGCGAAGGG
			ATTGAGATGGGGGATCACCTCTGGATAGCACGTTT
			CATCCTCCACCGGGTGTGCGAAGACTTTGGTGTCAT
			TGTGTCCTTCGATCCCAAACCCATCCCTGGGAACTG
			GAACGGTGCTGGCTGTCACACCAACTTCAGCACCA
			AGAACATGAGGGAAGATGGAGGTCTCAAGCACAT
			CGAGGAGGCCATCGAGAAGCTGAGCAAGCGCCAC
			CAGTACCACATCCGTGCCTACGACCCCAAAGGAGG
			GCTGGACAACGCCCGGCGCCTGACGGGCTTCCACG
			AGACGTCCAGCATCCACGAGTTCTCCGCCGGCGTG
			GCCAACCGCGGCGCCAGCATCCGCATCCCACGCAA
			CGTGGGCCATGAGAAGAAAGGCTACTTCGAGGACC
			GCGGGCCTTCAGCCAACTGCGATCCCTACGCCGTG
			ACGGAGGCCCTGGTCCGTACGTGTCTCCTCAACGA
			AACCGGGGACGAGCCTTTTGAGTACAAGAACTAa
			(SEQ ID NO: 24)
IGF2	Chicken	NM_001030342	ATGTGTGCTGCCAGGCAGATACTGCTGCTACTGCT
	[Gallus		GGCCTTCCTGGCCTATGCGTTGGATTCAGCTGCGGC
	gallus]		GTATGGCACGGCGGAGACCCTCTGCGGTGGGGAGC
			TGGTGGACACACTGCAGTTCGTCTGTGGGGACAGG
			GGCTTCTACTTCAGTAGACCAGTGGGACGAAATAA
			CAGGAGGATCAACCGTGGCATTGTGGAGGAGTGCT
			GCTTTCGGAGCTGTGACCTGGCTCTGCTGGAAACCT
			ACTGTGCCAAGTCCGTCAAGTCAGAGCGTGACCTC
			TCCGCCACCTCCCTCGCGGGCCTCCCAGCCCTCAAC
			AAGGAGAGCTTCCAGAAGCCATCTCATGCCAAGTA
			CTCCAAGTACAACGTGTGGCAGAAGAAGAGCTCGC
			AGCGGCTGCAGCGGGAGGTGCCAGGCATCCTGCGT
			GCCCGTCGGTACCGGTGGCAGGCGGAGGGGCTGCA
			AGCAGCTGAGGAAGCCAGGGCGATGCATCGTCCCC
			TCATCTCCTTGCCCAGTCAGCGGCCCCCAGCGCCGC
			GGGCATCCCCTGAAGCGACCGGCCCCCAGGAATGA
			(SEQ ID NO: 25)
TERT	Cow	NM_001046242.1	ATGCCGCGCGCGCCCAGGTGCCGGGCCGTGCGCGC
	[Bos		CCTTCTGCGGGCCAGCTACCGGCAGGTGCTGCCCC
	taurus]		TGGCCGCCTTCGTACGGCGCCTGCGGCCCCAGGGC
			CACCGGCTTGTGCGGCGCGGGGACCCGGCGGCCTT
			CCGCGCGCTGGTGGCTCAGTGCTTGGTGTGCGTGC
			CCTGGGACGCGCAGCCGCCCCCTGCCGCCCCGTCC
			TTCCGCCAGGTGTCCTGCCTGAAGGAGCTGGTGGC
			CAGAGTCGTGCAGAGGCTCTGCGAGCGCGGCGCGA
			GGAACGTGCTGGCCTTCGGCTTCACGCTGCTGGCC
			GGGGCCCGCGGCGGGCCGCCCGTGGCCTTCACGAC
			CAGCGTACGCAGCTACCTGCCCAACACGGTAACCG
			ACACGCTGCGCGGCAGCGGCGCCTGGGGGCTGCTG
			CTGCACCGCGTGGGCGACGACGTGCTCACCCACCT
			GCTGTCGCGCTGCGCGCTCTACCTGCTGGTGCCCCC
			GACCTGCGCCTACCAGGTGTGTGGGCCGCCGCTCT
			ATGACCTCCGCGCCGCCGCCGCCGCCGCTCGTCGG
			CCCACGCGGCAAGTGGGCGGGACCCGGGCGGGCTT
			CGGACTCCCGCGCCCGGCCTCGTCGAACGGCGGCC
			ACGGGGAGGCCGAAGGACTCCTGGAGGCGCGGGC
			CCAGGGCGCGAGGCGGCGTCGCAGTAGCGCGCGG
			GGACGACTGCCTCCAGCCAAGAGGCCCAGGCGCGG
			CCTGGAGCCCGGGCGGGATCTCGAAGGGCAGGTGG
			CCCGCAGCCCGCCCCGCGTGGTGACACCTACCCGA
			GACGCTGCGGAAGCCAAGTCTCGGAAGGGCGACGT
			GCCCGGGCCCTGCCGCCTCTTCCCGGGCGGCGAGC
			GGGGTGTCGGCTCCGCGTCCTGGCGGCTGTCACCC
			TCGGAGGGCGAGCCGGGTGCCGGAGCTTGCGCTGA
			GACCAAGAGGTTCCTTTACTGCTCCGGCGGTGGCG
			AACAGCTGCGCCGCTCCTTCCTGCTCTGCTCCCTGC
			CTCCCAGCCTGGCCGGGGCGCGGACACTCGTGGAA
			ACCATCTTTCTGGACTCGAAGCCCGGGCCGCCAGG
			GGCTCCCCGCCGGCCGCGCCGCCTGCCCGCGCGCT
			ACTGGCAGATGCGGCCCCTGTTCCGGAAACTGCTT
			GGGAACCACGCGCGGAGCCCCTATGGCGCGCTGCT
			CAGGGCGCACTGCCCGCTGCCGGCCTCTGCGCCCC
			GGGCGGGGCCAGACCATCAGAAGTGCCCTGGTGTT
			GGGGGCTGCCCCTCTGAGAGGCCGGCCGCTGCCCC
			CGAGGGCGAGGCGAACTCAGGGCGCCTGGTCCAGC
			TGCTCCGCCAGCACAGCAGCCCCTGGCAGGTGTAC
			GGGCTCCTGCGGGCCTGTCTTCGCCGCCTGGTGCCC
			GCCGGCCTCTGGGGCTCCCGGCACAACGAGCGGCG
			CTTCCTGCGGAACGTGAAGAAGCTCCTCTCCCTGG
			GGAAGCACGGCAGGCTCTCGCAGCAGGAGCTCACG
			TGGAAGATGAAGGTGCAGGACTGCGCCTGGCTGCG
			CGCGAGCCCAGGGGCTCGCTGCGTGCCCGCCGCGG
			AGCACCGCCAGCGCGAGGCCGTCCTGGGTCGCTTC
			CTGCACTGGCTGATGGGCGCCTACGTGGTGGAGCT
			GCTCAGGAGCTTCTTCTACGTCACAGAGACCACGT
			TCCAGAAGAACCGGCTCTTCTTCTTCCGGAAGCGC
			ATCTGGAGCCAGCTGCAGCGCCTGGGCGTCAGACA
			ACACTTAGACCGTGTGCGGCTTCGAGAACTGTCAG
			AAGCAGAGGTCAGGCAGCACCAGGAGGCCAGGCC
			GGCTCTGCTGACATCCAGGCTCCGTTTCGTCCCCAA
			GCCCGGCGGGCTGCGGCCCATCGTGAACGTGGGCT
			GTGTTGAGGGCGCCCCGGCACCGCCCAGAGACAAG
			AAGGTGCAGCATCTCAGCTCACGGGTCAAGACGCT
			GTTCGCGGTGCTGAACTACGAGCGAGCTCGGCGGC
			CTGGCCTCCTGGGGGCCTCGGTGCTGGGCATGGAC
			GACATCCACAGGGCCTGGCGGGCCTTCGTGCTGCC
			CCTGAGGGCCCGGGGCCCAGCCCCCCCGCTCTACT
			TCGTCAAGGTGGACGTGGTGGGGGCCTACGATGCC
			CTCCCCCAGGATAAGCTGGCAGAGGTGATCGCTAA
			CGTGCTGCAGCCGCAGGAGAATACGTACTGCGTGC
			GCCACTGCGCCATGGTCCGGACTGCGCGCGGGCGC
			ATGCGCAAGTCCTTCAAGAGACACGTGTCCACCTT
			CTCGGACTTCCAGCCGTACCTGAGGCAGCTCGTGG
			AGCATCTGCAGGCGATGGGCTCCCTGAGGGACGCC
			GTGGTCATCGAGCAGAGCTGCTCCCTGAACGAGCC
			TGGCAGCAGCCTCTTCAACCTCTTCCTGCACCTGGT
			CCGCAGCCACGTCATCAGGATCGGGGGCAGGTCCT
			ACATCCAGTGTCAGGGGATCCCCCAGGGCTCCATC
			CTGTCCACCCTGCTCTGCAGCTTCTGCTATGGGGAC
			ATGGAGAACAAGCTCTTCCCTGGAGTCCAGCAGGA
			CGGGGTGCTTCTGCGCCTGGTGGACGACTTCCTGCT
			GGTCACCCCACACCTGACGCGGGCCAGAGACTTCC
			TCAGGACGCTGGTGCGCGGTGTGCCTGAGTATGGC
			TGCCAGGTGAACCTGCGGAAGACGGTGGTGAACTT
			CCCCGTGGAGCCCGGGGCCCTGGGCGGCGCGGCGC
			CCCTGCAGCTGCCGGCCCACTGCCTGTTCCCCTGGT
			GCGGCCTGCTGCTGGATACCCGCACCCTGGAGGTG
			CATGGCGACCACTCCAGTTATGCCCGGACGTCCAT
			CAGAGCGAGTCTCACCTTCACCCAGGGCTTCAAGC
			CCGGGAGGAACATGCGTCGCAAGCTGTTGGCGGTC
			TTGCAGCTCAAGTGCCATGGGCTCTTCCTGGACCTG
			CAGGTGAACAGTCTGCAGACGGTCTTCACAAACGT
			TTACAAGATATTCCTGCTGCAGGCCTACAGGTTCCA
			CGCCTGCGTGCTGCAGCTGCCCTTCAGCCAGCCGG
			TCAGGAGCAGCCCCGCGTTCTTTCTCCAGGTCATCG
			CCGACACCGCATCCCGCGGCTACGCCCTCCTGAAA
			GCCAGGAACGCAGGGGCGTCACTGGGGGCCAGGG
			GCGCCGCCGGCCTGTTCCCGTCTGAAGCTGCGCAG
			TGGCTGTGTCTCCACGCCTTCCTGCTCAAGCTGGCT
			CGCCACCGTGTCACCTACAGCCGCCTGCTGGGGGC
			CCTCCGGACAGCCCGAGCACGGCTGCACCGGCAGC
			TCCCGGGGCCCACACGGGCCGCCCTGGAGGCGGCG
			GCCGACCCCGCCCTGACCGCAGACTTCAAGACCAT
			CTTGGACTGA (SEQ ID NO: 39)
TERT	Porcine	NM_001244300.2	ATGCCGCGCGCGCCCCGGTGCCGGGCCGTGCGCTC
	[Sus		CCTGCTCCGGGACCGCTACAGGCAGGTGCTGCCGC
	scrofa]		TGGCCACCTTCGTGCGGCGCCTGGGCCCTGAGGGC
			CGGCGGCTTGTTCGGCGCGGGGACCCGGCGGCCTA
			CCGCGCGCTGGTGGCGCAGTGCCTGGTGTGCGTGC
			CCTGGGACGCGCAGCCGCCTCCTGCCTCCCCGTCCT
			TCCGCCAGGTGTCCTGCCTGAAGGAGCTGGTGGCC
			AGGGTCGTGCAGAGGCTCTGCGAGCGCGGCGCGAG
			GAACGTGCTGGCCTTTGGCTTCGCGCTGCTGGACG
			GGGCTCGCGGCGGGCCGCCCGTGGCCTTCACGACC
			AGCGTGCGCAGCTACCTGCCCAACACCGTGACCGA
			CACACTGCGCGGGAGCGGCGCGTGGGGGCTGCTGC
			TGCGCCGCGTGGGCGACGACGTGCTCACCCACCTG
			TTGGCGCGCTGCGCGCTGTACCTGCTGGTGCCCCCG
			AGTTGCGCCTACCAGGTGTGCGGGCCGCCACTCTA
			TGACCTCTACACCGCAGCGGAGGCTCGGCCCATGC
			GACACAAGGGCCAGACCCCGACTGGCCTCGGACTC
			ACGCGCCCCGTTTGCAATGGGGAAGCCGGGCGACC
			CCAGGAGCAGAGGGCGCAAGGTGTGAGGCGACGT
			CGGGGCAGAGCGGGGGGACATCCACTTCCAGCCAA
			GAGGCCCAGGCACGTCCCGGAGCCTGAACAGGGTC
			CCGAAGGGCAGGCGTCCCGGGCCCACCAGGGCAG
			GGCGCCTGGGCCGAGCGACAGCGACCCCCCCGTGA
			TGACACCTACCAGAGCCGCTGCGAAAGCCAAGTCT
			CGGGAGGGTGAGGCGCCCGGAACCCGGCACCTTTC
			CCCTCAAGCAGGCGGTGCGCGGGGTACCTGCCCCC
			CATCCTGGTGGCAGCCACACCTCCAGGGCAAGCCC
			AGTCCTCATGTGTGCGCTGCCGAGACCAAGCGCTT
			CCTCTACTGCTCGGGGAGCAAGGAAGGGCTGCGCC
			GCTCGTTCCTGCTCTGCTCCCTGCCGCCCAGCCTGG
			CGGGGGCCGGGAGGCTCGTGGAGGTCATCTTTCTG
			GCCTCAAAGCCCGGGCAGCCAGGGGCGCGCCGCGT
			GCCCGCACGCTACTGGCGGATGAGGCCCCTGTTCC
			GGGAGCTGCTTAAGAACCACGCGCGGTGCCCCTAC
			AAGGCGCTTCTCAGGGCGCACTGCCCGTTGCGGGC
			TGCGGCGACCCTCTCGGGGTCCGGCGGTCAGGTGT
			GCGACCACAAAGTGGGCCCCCTCGCTCCAGAGCGG
			CTGGCAGCGGCCGCCGAGGGGGACTCGGCCTCGAG
			GCGCCTAGTCCAGCTGCTCCGCCAGCACAGCAGCC
			CCTGGCAGGTGTACCGCCTCCTGCGGGCCTGTCTTC
			ACCGGCTGGTGCCCCCGGGCCTCTGGGGCTCCCCG
			CACAACAAGCGGCGCTTTCTGAAGAATGTGAAGAA
			GCTCGTCTCCCTGGGGAAGCACGCCAGGCTCTCGC
			TGCAGGAGCTGATGTGGAAGATGAAAGTGCAAGA
			CTGCATCTGGCTGCGCCGGAGCCCGGACGCTCGCC
			ATGTCCAGGCCGCCGAGCACCGTCTGAGAGAGGCC
			ATTCTGGCCAAGTTCCTGCGCTGGTTGATGGGCAC
			GTACGTGGTCGAGCTGCTCAGGTCGTTTTTTTATGT
			CACGGAGACCACGTTTCAGAAGAACCGGCTCTTCT
			TCTTCCGGAAGCGCATCTGGAGCCGGCTGCAGAGC
			GCAGGCATCAGGCAACACTTAGATCGTGTGCGGCT
			TCGAGAACTGTCGGAAGCAGAGATCAGGCGACGCC
			GGGAGGCCAGGCCCGCTGTACTGACCTCCAAGCTC
			CGCTTCGTCCCCAAACCCGACGGGCTGCGGCCCAT
			CGTGAACATGGCGAACGTCGTGCGAGCCAGGACAG
			GCCCCGGAGACAAGAAGGTCCGGCGTCTCACGGGG
			CAGGTCAAGACGCTGTTTGCTGTGCTGAACTACGA
			GCGGGCGCGGCGCCCGCGCCTCCTGGGGGCCTCCG
			TGCTGGGCGTGGGTGACATCCACAGGGCCTGGCGG
			GCCTTTGTGCTGCCCCTGCGGGCCCAGGACCCGGC
			CCCCCCGCTGTACTTTGTCAAGGTGGACGTGACGG
			GGGCCTACGACGCCCTCCCTCAGGACAGGCTGCTG
			GAGGTGGTCGCCAACGTGATCCGGCCCCACGAGAG
			CACGTACTGCGTGCGCCAGTGCGCCGTGCTCCGGA
			GGACCGCCCGCGGGCACGTGCGCAAGTCCTTCCAA
			ACCCACGTGTCCACCTTCGCAGACCTCCAGCCTTAC
			ATGAGACAGTTTGTGGCACACCTGCAGGCAACCGG
			CCCGCTGAGGGACGCCGTGGTCATCGAGCAGAGCT
			GCTCTCTGAACGAGGCCGGCAGCCGTCTCCTGGAG
			CTTTTCCTGAGCCTGCTGCGAAACCACGTCATCCGG
			ATCGGGGGCAGGTCCTACGTCCAGTGTCAGGGGAT
			CCCACAGGGCTCCATTCTGTCCACGCTGCTCTGCAG
			CCTGTGCTACGGGGACATGGAAAACAGACTCTTCC
			CCGGGATCCAGCGTGACGGGGTGCTCCTGCGCTTG
			GTGGACGACTTCCTGCTGGTGACCCCTCACCTGAC
			ACGAGCCAAAGCCTTTCTCAGGACCCTGGTCCGCG
			GCGTGCCCGAGTACGGCTGCCTGGCCAACTTGCGG
			AAGACGGCCGTGAACTTCCCTGTGGAGGACGGCGC
			CCGGGGCGGCCCGGCCCCACTGCAGCTGCCGGCAC
			ACTGCCTGTTCCCCTGGTGCGGGCTGCTGCTGGACA
			CCCGCACGCTGGAGGTGCACTGCGACTATGCCAGT
			TACGCCCGGACCTCGATCAGAGCGAGTCTCACCTT
			CAACCAGGGCTTCAAGCCCGGGAGGAACATGCGCC
			GCAAGCTCTTGGCGGTCTTGCGGCTAAAGTGCCAC
			GGGATCCTTCTGGACCTGCAGGTGAACAGTCTTCC
			GACGGTGCTCGCCAACGTTTACAAGATCTTCCTGCT
			GCAGGCCTACAGGTTCCACGCGTGTGTGCTGCAGC
			TGCCCTTCCGTCAGCCGCTTGCGAGGAACCCCTCAT
			TTTTCCTCCGGCTTGTCTCCGACACCGCGTCCTGCT
			GCTACTCGCTCCTGAAAGCCAGAAACGCAGGGATG
			TCCCTGGGAGCCAGGGGCGCCTCCGGCCCGTTTCC
			CTCTGAAGCCGCAGAGTGGCTCTGCCTCCACGCCTT
			CCTGCTCAAGCTGGTTCGTCACCGCGTTACCTACAG
			CTGTCTTCTGGGGCCGCTCCGGGCAGCCAGAGAGC
			GATTGTGCCAGCGGCTCCCTGGGGCCACACTGGCC
			GCCCTCGAGGCCGCCGCCGACCCAGCCCTGACTAC
			AGACTTCCGGACCATCCTGGACTGA (SEQ ID NO:
			40)
TERT	Zebrafish	NM_001083866.1	ATGTCTGGACAGTACTCGACAGATGGCGGATTTAG
	[Danio		GCCGGTTTTGGAGATTCTGCGCTCCTTATATCCGGT
	rerio]		CGTGCAGACTTTGGAGGAGTTCACCGACGGACTGC
			AATTCCCTGACGGCCGAAAGCCGGTTCTGCTGGAG
			GAAACAGACGGCGCGCGCTTTAAAAAGCTCCTCAG
			TGGACTTATTGTATGTGCGTACACGCCGCCGCAGCT
			GCGCGTCCCCGCCCAGCTCAGCACCCTGCCGGAGG
			TCTTGGCGTTCACTCTGAACCACATTAAACGTAAG
			AAACTGAGGAACGTCCTGGGCTTCGGTTATCAATG
			CAGCGACGTGACGACCAGTTCGGATCCCTTCCGTTT
			CCATGGCGACGTTTCGCAGACGGCTGCCTCCATCA
			GCACCAGCGAGGTCTGGAAGCGTATCAACCAGCGT
			CTGGGCACGGAGGTAACGCGGTACCTGCTGCAGGA
			CTGTGCCGTTTTCACCACCGTCCCGCCATCGTGTGT
			TCTGCAGGTGTGCGGAGAACCTGTTTACGACTTGCT
			GATGCCGCGCTCATGGTCTGGCTTTTTCCTCAGTAA
			CTCAGATAATGAACGAATCAGCGGCGCGATGCGGA
			AATTCCCTGCTGTCCAGAAGACAGTCGCAATTTCC
			AAAAAGAGAACAAGAGATAACGAAAAATATATTT
			CGGTAAAGCGGCGGAGGGTAAAGGAAACTGTGAA
			TAATAATAACGGAAATTACAGATCTCTGTGTTTTGC
			AATTTCTAAAAAGAGAGCGATAGATAATGAAGAA
			AATATTTCGTTAAAGCGACGGAGGATGGAGGAAAC
			TGACCAAGTAGCGAAAATACGTAATGAAAATCACG
			AATCTCAGAGTTTCGCAATTTCTAAAAAGAGAGCG
			AGAGATAATGAAGAAAATATTTCGTTAAAGCGACA
			AAGGATGGAGGAAATTGACCAAGTAGCGAAAATA
			CGTAACGAAAATCATGGATCTCAGAGTTGGAAACC
			AGCAGATCAGCGTCCTCCTCGACCCTCGCAATGTTC
			AATACGCGTTCTGAGCATGCTCTACAATGGGCGGG
			GCATGAAGAACTTCCTGCTCAACAGGAAGTTGAAA
			GGAGTGGGCGGGGCCAGGCGCATGCAAGGGGAGG
			ATCTTGTCCGCATGATTTTCCTCCAATCAGAATCCA
			ACGACAGCAAACCGAAAAAACTTCCCAAACGATTC
			TTCGCAATGGTGCCGCTATTCAGTCGGCTGTTGCGG
			CAGCACAGGAAGTGTCCGTATCGGCTGTTCCTGCA
			GAGGAAGTGTGCAGGAAATCCAGACGTGAAGGAT
			ATGGAGTCTCTGCTGAAGTCACACTCGTCTCCATAT
			AGAGTTTATCTGTTCGTCAGGGAGTGTCTGCGCCAT
			ATTATTCCCCACGAGCTCTGGGGCTGCCAGGAAAA
			CCAGCTCCACTTCCTGTCTAATGTAAAGAACTTCCT
			GCTTCTGGGGAAGTTTGAGCGCCTCACGCTGGTCC
			AGCTGATGTGGAGGATGAAGGTTCAGGCCTGCCAT
			TGGCTGGGGCCCAAGAAACGTCAGTGTGCGAGCGA
			GCACCGCTACCGTGAGTGGATGTTGGGTCAGTGTA
			TGGGCTGGATGTTGAGTGGTTTTGTGGTCGGTCTGG
			TCAGAGCTCAGTTCTACATCACGGAGAGTATGGGC
			CACAAACACACACTGCGCTTCTACAGGGGAGATGT
			CTGGAGCAGACTGCAGGACCAGGCCTTCAGGGCTC
			ATCTGTGTAAGGGCCAGTGGAGGCCCCTGTCTCCA
			TCCCAGGCGCTGAAGGTCCCCAATAGTGCAGTGAC
			ATCCCGCATCCGCTTTATTCCCAAAACCAGCAGCAT
			GAGGCCCATCACACGCCTCAGCGGCAGCAGAGACA
			CACTGCAGTATTTTCAGAGCTGTGTGCGTGTGCTGC
			AGAATGTGTTGAGTGTGTGTGTGCGTGAGGCCCCG
			GGGCCCATGGGCTCCACCGTCTGGGGTTGGCAGGA
			CATTCACAGACGCCTGCAAGACTTCAGCCCTCAGC
			AGAAGAGCTCGCCACGACCGCTCTACTTCGTCAAG
			GTGGATGTGAGCGGAGCGTATGACAGTCTCCCGCA
			CCTGAAGCTGGTGGAGGTGCTGAAGGAAGTGTTGG
			GTCCGTTTGCAGAGCAGAGCTTCTTCCTGCGTCAGT
			ACAGCAGTGTGTGGAGCGACCCGACCCGCGGCCTG
			CGCAAACGCTTCTGCACCAAAGCTGAGATGTCAGA
			GCCGCTCAACATGAAGGGGTTTGTTGTGGATGAAC
			AGGTCAGCGGGCGCCTGCATGACGCTATATTAGTG
			GAGCGGCACTCGTCTGAGGTCAGAGGTGGAGACGT
			CTTCCAGTTCTTCCAGAAGATGCTCTGCAGTTACGT
			CATCCATTACGACCAGCAGATGTTCCGGCAGGTGT
			GTGGGATCCCGCAGGGCTCTTCAGTGTCTTCTCTGC
			TGTGTAATCTGTGTTACGGACACATGGAGAAAGCC
			CTGCTGAAGGACATCGCTAAAGGAGGGTGTCTGAT
			GAGGCTGATTGATGATTTTTTGCTCATTACTCCTCA
			TCTGAGTAAAGCCACAGAGTTCCTGACCACTCTTCT
			GTCTGGAGTTCCAGATTACGGTTGCCAGATTAACC
			CTCAGAAGGTGGCGGTGAACTTCCCCGTGTGTGTG
			TCCTGGGTAAACTCGGGCGTCTCTGTGCTGCCGTCC
			AGCTGCCTGTTCCCCTGGTGCGGCTTGATGATACAC
			ACACACACGCTGGACGTCTATAAAGACTACTCACG
			GTATGACGGCCTATCACTGCGCTACAGCCTGACTCT
			TGGCTCCGCCCACTCTCCATCTACAGTCATGAAGA
			AGCTGCTGTCGGTGCTCAGCATCAAAAGCACGGAC
			ATCTTCTTAGACCTCAGGCTGAACTCTGTGGAGGCC
			GTTTACAGGAGTCTGTATAAGCTGATTCTGCTGCAG
			GCGCTCAGGTTTCATGCGTGCGTGAGGAGTCTGCC
			GTTGGGTCAGAGTGTGAACAGAAACCCGTCGTTCT
			TCCTGAAGATGATCTGGAGAATGACTCGAGTCACC
			AATAAACTCCTCACACACATTAACAAAGGTCTGCC
			TGTGTGTTCTGTGGACAGTGGTGGTGTTCTGCAGTC
			TGAGGCGGTTCAGCTTTTATTCTGTTTGGCCTTCGA
			GACGCTTTTCAGACGGTTTCGCTCGGTTTACCACTG
			CCTGATCCCTGCACTGCACAAACGGAAGCGTGCTC
			TTCAGCGTGAGCTCTGCGGGATCACTCTGGCTCGG
			GTCCGTCAAGCTTCCTCTCCCAGAATCCCCCTGGAT
			TTCAGCATGCGGGTGTAA (SEQ ID NO: 41)
TERT	Tilapia	XM_003458511.4	ATGACGCGGGCCCTTAAAAGGTCAAACATAGCTAA
	[Oreochromis		ATCCCAGTGTAAAGTAGCTAACCTCCGTCCAAGTG
	niloticus]		CTCCGAACACAGTCGGTATGTCTGCGACTGATATG
			TCCGGTGTGCTGGATATCCTTCGGTTACTGTACCGG
			CACACGCAGACACTGGAGGAGTTTTCGGACAGCAT
			CGTGTTCAGAGAAGGACAGAAAGCAGCTCTCATTG
			AGCAGACAGATACAAACCGATTCAAATCTTTCGTT
			AGGAGTGTTTTTGTGTGCTTTGACAAGGAGCTACA
			GCAGGTAGCGAGCTGTAAACAGATCTGCAGTCTGC
			CTGAACTACTGGCGTTTGTTCTCAACACTCTAAAAA
			GAAAAAGAAAAAGGAATGTCTTGGCACATGGCTAT
			AACTTTCAGACCCTGGCTCAGGAGGATCGGGATGC
			AGACTTCCTCAAATTCCAAGGCGACGTAACACAGA
			GTGCTGCCTACATCCACGGCAGTGACCTGTGGAAA
			AAAGTCACAATGCGTCTGGGCACAGACATCACGCA
			ATATCTTCTGGAGAGCTGCTCTGTGTTTGTGGCAGT
			TCCTCCTTCGTGTGTTTTCCAGGTGTGCGGCCCTCC
			AGTCTATGACAGGGTGTCCATGACCATGGCCTCGA
			GTGGGTTTTTTCTCCAGCCTGGAGTCAGGAAACAT
			AATCGTACCAAGATTGAGAGCTGTCGAGGGTCAGT
			GAGTTTGAAACAGAAACGCACAGTTGTGAATCCTG
			CTGCAAGCAAGAAGATGAAAAGAAGGAATAAAGG
			AGGGAAAAAAGGGAAAAGAAAACGGGAAACTGGT
			GAAGAGGAGGAGGTGGCGGTTTGTTCAAGAAAGA
			GGCGGCGAGTAGCGTCTATAGAACATCAACAGGCG
			ATCCAACCAGTTGGCTCTGAAAAGGAAGGACAGGT
			TGTGCCTGTGGAATCAGCACCGCCTGCAGCTTTCA
			AACAGCCTGTTGAAATGCCAACATTGGAGGGCGGT
			CCTAGTTGGAGATCAGGGATTTTCCCCCCTTTACCA
			CCCTCGCAATGTTTTATCCGCACCCTGGGATTCCTG
			TATGGGGGCAGGGGCATGCGTGGCTTTCTTCTTAA
			CAGGAGGAAGAAGACTGCTCATGGATCCAGAAGG
			CTTCAAGGACAAGATCTGGTAAGAATAGTCTTCTT
			CGAGGGACTAGCGTATTTGAATGGAGTAGAGAGGA
			AGCCTAAAAAACTCCCCCAGAGGTTCTTTGGCATG
			GTCCCCCTGTTTAGGCAGCTCTTACAACAACACAG
			GAGCTGTTCCTACACCAAAATACTACAGAGGTTAT
			GTCCATCAATAGAGGAGAGCAATGCAGGACAGGG
			AGAACTAAACTCACTCTTACCTCAGCACTGTGCAC
			CGCACAGGGTTTACCTGTTTGTCCGGGAATGCCTCT
			CTTCTGTGATCCCGCAAGAACTGTGGGGCTCTGATC
			AAAACCGGCTGCATTTCTTTGCCAGGGTCAGGACT
			TTCTTGCGAAGTGGCAAGTTTGAGAGGCTCTCACT
			GGCTGAACTGATGTGGAAGATAAAGGTGAATGACT
			GTGATTGGTTGAAGAGGAGTAAAACAGGCTGTTTT
			CCACCCAGCGAGCTTGCGTATCGGACACAGGTCCT
			GGGTCAGTTCTTGGCTTGGCTTCTGGATGGATATGT
			TACAGGCCTTGTGAGAGCCTGTTTCTATGCAACAG
			AGAGTATTGGGCAAAAAAACGCCATCAGGTTCTAC
			AGGCAGGAAGTCTGGGCCAAACTGCAAGACTTGGC
			CTTCAGAGGTCACCTTTCCAAAGGCCAGATGGAAG
			AGCTGACTCCAGCTCAGGTGGCATCCCTGCCCAAA
			GGCACCGTCATCTCCCGCCTTCGCTTTATTCCCAAG
			ACTGATGGCATGAGGCCCATCACACGAGTCATAGG
			AGCAGATGCCAAAACAAGGCTCTACCGAGGCCGTG
			TCAGGGACTTGCTGGATATGCTGCGGGCCTGTGTG
			CGTGCCACTCCATCACTGCTGGGGTCCACAGTGTG
			GGGGATGACTGACATCCACAAGGTTTTGTGCTCTTT
			GGCACCAGCGCAGAAGGAAAAACCACAACCCCTCT
			ATTTTGTTAAGGTGGACGTGAGTGGAGCCTATGAG
			AGTTTGCCGCATGACAAACTCATAGAGGTGATTGG
			CCAAGCCCTGTCACCTGTCCACGATGAACTCTTTAC
			CATCCGCCGCTATGCCAAGATCTGGGCGGACTCCC
			ACGAAGGCCTGAAAAAGGCCTTTGTCAGACAGGCA
			GATTTCCTGGAGGATAACATGGGATCCACCAACAT
			GAAGGGCTTTTTGACGTCACTGCAGAGAAAAGGCA
			AAGTTCATCACGCCATCCTGGTTGAGCAGCACTTTT
			GCTCAGATCTTCATGGCAGAGAGGCATTGCAGTTC
			TTTACCCAAATGCTAACTGGCAGTGTTGTTCAGTAT
			GGGAAAAAGACGTACCGTCAGTGCCGGGGGATTCC
			TCAGGGATCGGTTGTGTCTAGTCTGCTCTGCTGCCT
			TTGCTACGGCCACATGGAGAATCTCCTGTTTAAAG
			ATATTCCTGGACACAAAGGGTGTTTGATGAGACTG
			GTGGATGACTTCCTTCTGATCACACCAGACCAACA
			TGAAGCACAAGCTTTTCTCAAGATCTTGCTGGCCG
			GAGTGCCACAGTATGGTCTGGCGGTCAACCCGCAG
			AAGGTGGTTTTGAACTTTCAGGTATCGGGAAGCGT
			GGCCTCCTGTCCCGACATTCGCATCCTGCCCCCTCA
			CTGCCTCTTCCCCTGGTGTGGACTGCTGCTGGACAC
			CCACAAGCTGGACGTCTATAAAGACTATTCCAGCT
			ATGCTGGACTGTCTCTGCGCTACAGCCTTACTCTGG
			GTTCATCCCACTCTGCAGGACAGCAGATGAAAAGG
			AAACTAATGGCTATCCTCAGGCTCAAGTGTCATGC
			CCTGTTCTTCGACTTGAAGACTAATTCTCTTGAAGC
			GGTCTACAAGAACATCTACAAGCTGGTGCTGCTGC
			ATGCGTGCAGGTTTCATGTCTGTGCCCAAAGCTTGC
			CCTTTGGTCAGACCGTTTCCAAGAACCCCGTCTTCT
			TTCTGCAGTTGATATGGGAGATGGCCCAGTACTGC
			AACAAGCTCATCAGACGCAGCAACAAAGGACTGAT
			TTTAGGTGATAAGGCCCAGACGGGGATCGTGCAGT
			ACGAAGCAGTGGAGCTGCTTTTCTGTCTGTGCTTCT
			TGCTGGTGCTGTCACAACATCGTCTTCTCTATAAAG
			ATCTGCTCGCACACTTGCACAAGCGAAAGCGCAGT
			CTGGAGCGGCGTCTGGGGGACCTGAGGCTGGCCAG
			GGTGCGGCAGGCTGCTAGCCCCAGGACTCCAGTCG
			ACTTCTTGGCCATTCAGACATAA (SEQ ID NO: 42)
TERT	Rainbow	XM_021559758.1	ATGCCCAGTGGCGATATGACACGTGTGCTCGGCAT
	trout		ACTCGGCTCTCTGTATCGGCACGTCGAGACCCTGG
	[Oncorhynchus		AGGAGTTTGCAGACCATATTGTATTCAGAGAGGGA
	mykiss]		CAGAGAGCGGTGCTCATCGAACCGACAGATACAAC
			GCGCTTCATATCGTTTGTCCGGGGAGTGTTGGTCTG
			CACGGATAAAACCCTACAGGACGTCCCCAGCTGCA
			ATCAGATCAGCACCGTGCCTGAGCTGTTGGCGTTC
			GTGTTGAACAACATCAAGAGGAAAAAGAAAAGGA
			ATGTCCTGGCGCACGGTTACGGTTACACGTTCCAG
			GACCGCGACGCAGACCAGTTTAAGTTTCATGGCGA
			GATCACTCAGAGTGCCATGTACATCCACTGCAGCG
			ACTTATGGAAGAGGGCCTGCCAGCGCCTCGGCACG
			GACATCTCCAAGTACCTCCTGGAGAGCTGTTCTTTG
			TTCGTGACGGTGCCGCCGTCGTCCGCGTTCCAGGTG
			TGCGGCGTGCCTGTGTACGACCGCGTTTCCATGTCA
			ACGGGTATCTCTAGGTTCCACCTGGGATACAAACG
			GAATGGTACTACTAGGAACAGCAGAGGGAGAAGT
			AAGGAGGTCAGAAATGGGGGATGGGAATTTCAGG
			GTTCTGCTGGGAGAAATAGGAGAAAGGATGGAGG
			TAGAGACACTGGGAAAAGGAAGGGAGACGAGGTC
			AGTTTGGGAGGGAAGAGGAAGAGGGAGAGGGAGG
			AGGTGGAAGGAGATGTGTGTTTGCCTGGAAAAAGG
			AGATGCACTCAAAGAGAAGCTCCCACAGTCTCCAG
			TGGGACTAGCGATCGTAAGCACAGAACACTGGAAA
			CAAATGGGGTCAAGAGACCAGTGGAGGTCATTTCT
			CTCACCAAGGGACCCACACAGAGCCTACAGGTTTT
			CAATGGTTCTAGCAATGTGGAACAGGTGTCAGCAG
			AAATGGAACGTCTCAGGAAGCCAGTGGAGAAACT
			GGCTGGACCCGGAAGACCATTGGAGGCTGTGATGG
			TCACCATAGCACCCGCTGAGAGCTCTAAACAGGTC
			TCCAACGGCACAGGTAATATCGAGCAGATGTCAAT
			GAAAACAGGACATAGAAGGCCAGCGGCTGTAGTC
			CCAAGACCAGTAGAAGAACAGTCTGGACCTGTATC
			GGCCACCGTCCATGTAGAGGGGGGCCCTAGTTGGA
			GAACAGGGTCGTTCCCACCGCTTCCCCACTCCCAGT
			GTTTCATCCGCACCCTGGGCATGCTCTACGGAGGG
			CGGGGCATGCGCCGCTTCCTACTAAACAGGAAGAG
			GAAAAGTAGGGACGAGGGGCCCAGGCGTCTGCAG
			GGGCGAGACTTAGTGAGACTGGTCTTCTTTGAAGG
			CGTGGCCTATCTGAACGGAACAGAAAGGAAGCCTG
			AGAGACTTCCCAGAAGATTTTTCACCTTGGTGCCTC
			TGTTTTGTCAGTTGTTACGTCGACACAGGAGGTGTC
			CCTATTCTAAGATACTGCAGAGGGTTTGTCCAGCA
			GTGGGACAGGGGGATATGGCCTCCCTCCTGCCCCA
			GCACAGTGCACCTCACCGGGTGTACCTCTTTGTCAG
			AGAGTGCCTCAACGCGGTGGTCCCCTCGGAGTTCT
			GGGGGTCGGACCATAACCGATTCAAATTCCTGTCC
			GCAGTCAGGAACTTCCTGTCCATGGGCAAGTTTGA
			GAGGATGTCATTGGCTGAGCTGATGTGGAAGATGA
			AGGTGAATGACTGTGATTGGCTGAAGATCAGCAAG
			ACAGGCCGCTGCCCGCCCAGTGAGCTGTCGTATCG
			GACGCGGGTGCTAGGCCAGCTCCTGGCTTGGCTGC
			TGGATGGCTATGTGCTAGGCCTGGTGAGAGCTATG
			TTCTACGTCACAGAGAGCATGGGACAGAAGAACGC
			ACTGCGCTTCTACAGATACCAGGTCTGGGCCAAGC
			TGCAGGAGCTGGCTTTCAGTGGTCACCTCTCTAAA
			GGTCAGATGTCAGAGTTGACCCTGGCCCAGGTGAC
			GTCGCTCCCCAAAACCACTGTCCCCTCCCGCCTCCG
			CTTCATCCCCAAGACCGAAGGGATGAGACCCATCA
			CACGGGTCATAGGGGCTGACGCCAAAACAAGGTTG
			TTCCAGACCCGTGTGAAGGAGCTGTTAGATGTGCT
			AGGTGTCTGTGTACGGTCCTCTCCCTCTCTCCTGGG
			CTCTACAGTGTGGGGGTTGACCGACATCCACAGAG
			TCCTCTCTTCCATCACCCCTGCTCAGAAAGACAAAC
			CACAGCGGCTCTACTTTGTCAAGGTGGATGTGAGT
			GGGGCCTATGACAGTCTACCCCACACTCAGCTCTT
			GGAGGTGATTGGTCAGGTCCTGTCACATGTGCAGC
			AAGAGCTTTTCTCGGTGCGACGCTATGCCAAGGTG
			TGGGCCGACACCCACGAGGGCCTCAAGAAGACCTT
			TGTCAGACAGGCAGACTTCACGGAAGACACTGTGT
			CGTCCACCAACATGAAAGGCTTTGTGATGTCACTG
			CAGAGAGAGGGCAAAGTTCACGATGCCATACTGGT
			GGAGCAGCATTTCTCCACAGATATTCATGGCAAAG
			ACGTCTTGGAGTTCTTCACCCAGATGCTCTCTAGCT
			GTGTTGTCCAGTTTGGGAAGAAATCGTTCCGTCAGT
			GTCAGGGGATTCCTCAGGGTTCCGCGGTGTCGTCTC
			TGCTGTGCTGCCTCTGTTACGGCCACATGGAGAAC
			CTTCTGTTTCCTAACGTCAGTCGGCGAGGAGGGTGT
			CTGATGAGACTGGTTGACGATTTCCTCCTCATCACT
			CCTGACCTGAGCCAGGCACAGACCTTCCTCAAGAC
			CCTGATGGCGGGGGTACCACGGTACGGGTGTGTGG
			TGAACCCCCAGAAGGTGGCTGTTAACTTCCCTTTGG
			GTGAGTGGGGGTCCTGTCCTGCTGGGGTACGCCTG
			CTGCCTTTACACTGTCTGTTCCCCTGGTGTGGACTA
			TTGCTGAATACACACACCCTGGACGTCCACAACAA
			CTACGCCAGCTACGCTGGCCTATCCCTGCGCTACA
			GCCTGACGCTAGGCTCCGCCCACTGCGCGGGGCAG
			CAAATGAAGAGGAAGCTCATGTCCATCCTTAGATT
			CAAGTGCCACGCCCTCTTCCTGGACCTCAAAACCA
			ACTCCCTGGAGGCTGTCTATAGCAACGTCTACAAG
			TTAGTGTTGCTGCAGGCGTTCAGGTTCCATGCCTGT
			GCACAGAGTTTGCCGTTTGGTCAGAAAGTGGGCGG
			AAACCACTCGTACTTCCTCAATCTGATCTGGGACTT
			GGCGGAGTACACCAACCATCTAGTCAGACTCTGCA
			ACAAAGGTGTGTCTCTAGGCTGTAAGGCTTTAACA
			GGTAGCCTTCAGTATGAGGCAGTAGAACTGATATA
			CTGTCTGGCCTTCCTGTTGGTTCTGTCCCGTCATCG
			CCCCCTCTACTACCATCTCCTCGCTCCGCTACGCAC
			ACGTAAGAGGAAGCTGGAGGGGAAGCTGGAGGGT
			TTGAGATTGGCCCGAATCAGACAGGCTGCCACACC
			CAAAATGCCTGAAGACTTCAAGGCCATCCAGGCCT
			AG (SEQ ID NO: 43)
TERT	Tropical	XM_018094976.1	ATGACTCTGTGTACCGGAGGAGCTGAACTACTGAG
	clawed		CATTTTGCACAGCCTTTATGGCCAGGTCCTTGGGAT
	frog		TGTGGAATATATCGACTCACTGCATGTTCCCGGCG
	[Xenopus		GCATTAAGGTGCCTGTGCTGCGAGAGGGAGACCCG
	tropicalis]		GAGAAGTTCAAGTCATTTGTTGCGGAACTGATGCT
			GTGCATTCCAAGAGGAACAAAGTCGCTTCCGTCCC
			CTGTCTCCTTTCTTCAGCTATCAACTCAGAGAGAAG
			TAGTGGCGCGAGTAATTCAGCGGATTTGTGAAAAG
			AAAAGAAAAAATGTTCTTGCTTTTGGTTATGGCTTA
			GTTGATGAAAAAAGCTCTCTGAATATTCGATTGAC
			TCCAAATATTTGCAGTTATTTTCCTAATTCCACAAC
			AACAACAATCAGCACAAGTATTCTTTGGGAAACTC
			TGCTTACTAGAGTAGGTGATGATGTTATGATGTATT
			GGCTGGAACAATGCTCAGTTTTTGTATTTGTGCCAC
			CTAGTTGTTGTTATCAAATCAGTGGGCAGCCAATCT
			ACACTTTACCCTATGATAGTATGTGTTCATTTCGAT
			CTCAGTCATTTATGCATAGCAATGTTTTGTTGCAGT
			ACATTAAAAGAAATGCCTTTTTCTTGCGGAAAAAA
			TATCTGAAGCCAAAAAAGTGGTGGAAAACGGTGTT
			AAACAGCAAAGTAGAAAAACATTCAAAGACTTCTC
			AAATGCTAACATGGCAAAATAAAAAGTCCACATCA
			GCATTGCCTATTTGTAGTGAGTCATCTATGAAAGTT
			ACCACAAAAATACATTCCAAAAGGAAGATGTGTAC
			TACAGATATTTGTGACATTCCAACTAAGAAACGCA
			GAGTCAACTTGGACAAAGATGATAAAATGGACCAC
			GTTTCCTTTACGTCTGCATGTCTTTCTTCCTTCTCAA
			ATGTGTGCCCTGAAGCTAAAGTACAAGCAACGGAA
			TTTATTACCTCAAGATATGGAAAAAAAACAAAAAT
			TCAATGTCCAAAATCGACTTCATACTCAGTTGATGG
			TGAATTTAATGTAACTCTTCAAAATAATGCTAATAC
			GTTTATTACCAATGCTTCTGTCCCTACAATACAAAG
			CAAAACTTCATTTTCAAATATTTTTATTGAAATTGG
			AAGAACATTGTATTCAAGTATTAGTTTCAAGAAGG
			GCTTCTCTGAAAGTTTTATACTTAACAGTTTAGACT
			GTACCCCTTCTGGGAGCCAAAAATTAGTGGAAACC
			ATATTTCTAAACAACTTTTTAACTGAGCAAAATTTT
			GACCAGCCAAAACGGGATGAAAACTTTAGATCTAA
			ACTTCCCAAACGTTATTGGAGAATGAGAAAATATT
			TCCAAGAATTAATACAGAACCATAAGAATTTCCCT
			TATCTGGTATATTTGAATAAACACTGCCCTGTTAGG
			CCTTCAATGGCTTGTTCACACAAACTGGCGTTGCAG
			AAAAAGAATAAATGTAAAATGGATAAATCAATTTG
			TGACTTAAGTAATACCTCAGTTATGAAAAACAAAA
			TTGTAAATGATGAAAAGCCGCTAAAACATGTTACA
			GCCGAAGCAACTTTTTTACCTCTTCTTAAACAACAC
			AGCAGCAGTTGGCAAGTGTACATGTTTGTTAGAGA
			ATGTTTAAATAGTTTAGTGCCTGATTTCATATGGGG
			CTCCAGTCACAACAAGTGCCGTTTCCTTAGAAATGT
			AAAATCTTTTCTTTTTTTTTCTGGCAAATTTGGCAA
			GGTCTCTTTATTAGAGCTTATGTGGAAGATGAAAG
			TAGAAGACTGCTCTTGGATTCGTCTACGAAAAAGT
			GATCACTTTGTTCCTGCTTCAGAACACTTGCTACGA
			GAGAGAATCCTTGCCAAATTTATCTTTTGGCTAATG
			GACACCTATGTCATACAGTTGCTGAAATCATTTTTT
			TTTGTCACGGAAACCATGTTTCAGAAGAATAGACT
			TTTGTTCTACAGAAAAAGAATTTGGAAGAAACTTC
			AAAATTTAGGTCTAAGAAAACATCTAGAGAAGGTG
			AAATTGCGTCCATTGTCCTGCGATGAACTAGAAAA
			GATGCAACAATGGAAAAACATTCCACTGGTTTCCA
			GGCTCAGATTCATACCAAAAACAAATGGACTACGT
			CCAATATCTAGAGTATCCAGTACTTTGGGTAGCCA
			ACAAAGCAAAGAAAACCAAGAGAAGAAGATTCAA
			CATTTTACCTCTCGGGTTCGAAACCTTTTTAGTGTT
			CTTAACTATGAATGGAATAGAAATTGCAGCCTAAT
			TGGCTCATCTGTTTTTGGCATGGATGATATATACAA
			ACAGTGGAAAAAATTTGTGCTAGATTTTGAAAAAT
			CGAGAGCTGAAAAAGGCAAATTTTACTTTGTGAAG
			ACAGATGTTAAGGGAGCATATGATACCATTCCACA
			TTCAAAGCTCGATGAAGTGATCTTAAAAGTAATTA
			ATCCAAATGCAAATGAAGTATATTGCATACGACGT
			TATGCCTCAGTTTCAGTGGATTCAACTGGACGCATT
			ATAAAATCTTTCAAAAGACATGTATCTGCATTAGC
			AGATGTTCTTCCAAATATGAAACAGTTTGTTTCAAA
			TCAACAAGAAAAAAACTTGACACGTAACACAATTC
			TAGTGGAACAGAGCCTTTTATTGAATGAGAGCTCT
			GTCAAACTTCTTGCTGTTTTTCAACAAATGATCAGA
			TCCCATATTTTAAGAATAGAAGATCGATATTACAT
			GCAGTGCTGTGGAATACCACAGGGTTCAATGTTAT
			CTACAATCCTATGCAGTTTATGCTATGGAGACATG
			GAAAATAAACTGTTTGGCGGAATACAGCAAAATGG
			GGTACTAATGCGATTGATTGATGATTTTTTGTTTGT
			AACACCTCATCTTAACCAGGCAAAAACATTTTTAA
			GGACTCTGGCAGAAGGAATTCCCCAATATGGGTGC
			TCCATCAGCCCTCAAAAAACAGTGGTAAACTTTCC
			TGTTGATGACATCCCAGCATGCTCTGAGGTGGAAC
			AATTACCAGTTCACTGCTTGTTCCGGTGGTGTGGTC
			TTTTGCTGGACACTCAGACTTTGGATGTTTACTATG
			ATTATTCAAGCTATGCCTGTACCTCAATCCGATCAA
			GTATGACATTTTGTCACAGTTCTGCAGCAGGAAAA
			AACATGAAACAAAAACTTCTAAGAGTCCTTAAATT
			GAAGTGCCACAGTCTCTTTCTTGATTTACAGGTAAA
			CAGTTTAAGGACAGTTTTCATCAATACTTATAAGAT
			ATTCTTACTTCAAGCTTACAGATTCCATGCTTGTGT
			TGTTCAGCTTCCATTTGGCCAGCGTGTAATGAATAA
			TCCACCTTTTTTTCTTACTGTGATTTCTGATATGGCA
			CCTTGCTTTTACACTACTTTTAAGTCCAAAAACAAA
			GATGTCACACGTGGGTACAAGGATGTGAGCTGCCA
			GTTTAACTTTGAAGCAGTCCAGTGGCTCAGTTATCA
			AGCTTTTCTTACTAAGCTTCGCAATCACAAAATATT
			ATACAAATGTCTTATTGGGCCACTGCAGAACTGTA
			AAATGCAGTTATCTAGAAGACTTTCGCAGTATACT
			ATTGATCTTCTAAAAGCTGTCACAGATTCTTCCCTT
			CACAAAGACTTTTCATGTATAATGGATTAG (SEQ ID
			NO: 44)
TERT	Chicken	NM_001031007.1	ATGGAGCGCGGGGCTCAGCCGGGAGTCGGCGTGCG
	[Gallus		GCGGCTCCGCAATGTAGCGCGGGAGGAGCCCTTCG
	gallus]		CCGCGGTCCTGGGCGCGCTGCGGGGCTGCTACGCC
			GAGGCCACGCCGCTGGAGGCCTTCGTCCGGCGGCT
			GCAGGAGGGTGGCACCGGGGAGGTCGAGGTGCTG
			CGAGGCGACGACGCTCAGTGCTACCGGACCTTCGT
			GTCGCAGTGCGTGGTGTGCGTCCCCCGCGGTGCTC
			GCGCCATCCCCCGGCCCATCTGCTTCCAGCAGTTAT
			CCAGTCAGAGCGAAGTCATCACAAGAATCGTTCAG
			AGGCTGTGTGAAAAGAAAAAGAAGAACATCCTTGC
			GTATGGATACTCCTTGCTGGATGAGAACAGTTGTC
			ACTTCAGAGTTTTGCCATCTTCGTGTATATACAGCT
			ATCTGTCCAATACTGTAACAGAAACGATTCGCATC
			AGTGGCCTCTGGGAGATACTGCTGAGTAGGATAGG
			GGACGACGTGATGATGTACCTGCTGGAGCACTGTG
			CACTCTTCATGCTGGTTCCCCCAAGTAACTGTTACC
			AGGTCTGCGGGCAACCAATTTATGAACTTATTTCGC
			GTAACGTAGGGCCATCCCCAGGGTTTGTTAGACGA
			CGGTACTCAAGGTTTAAACATAATAGCTTGCTTGA
			CTATGTGCGAAAAAGGCTTGTGTTTCACAGGCACT
			ATCTTTCCAAGTCACAGTGGTGGAAGTGCAGGCCG
			AGACGTCGAGGTCGTGTCTCCAGCAGGAGAAAAAG
			AAGGAGCCATAGGATACAAAGCCTAAGGTCTGGTT
			ATCAGCCTTCTGCAAAAGTGAACTTTCAAGCAGGT
			AGGCAGATCAGCACTGTTACTGCACGTCTGGAAAA
			ACAGAGCTGCTCCAGTTTATGTTTGCCAGCTAGAG
			CACCATCTTTAAAAAGGAAGCGTGATGGAGAACAG
			GTTGAAATCACAGCTAAGAGAGTGAAAGTAATGGA
			GAAAGAGATAGAGGAACAGGCTTGTAGTATCGTTC
			CTGATGTAAACCAAAGTAGCTCCCAGAGGCATGGA
			ACCTCCTGGCATGTAGCACCACGTGCTGTAGGTCTT
			ATTAAAGAACATTACATTTCTGAAAGAAGTAACAG
			TGAGATGTCTGGTCCTTCTGTAGTTCGCAGATCTCA
			CCCTGGGAAGAGGCCTGTGGCAGACAAAAGCTCTT
			TTCCACAAGGAGTTCAGGGTAACAAACGCATAAAG
			ACCGGTGCAGAAAAACGAGCAGAATCCAATAGAA
			GGGGCATAGAGATGTATATAAACCCAATCCATAAA
			CCCAATAGAAGGGGCATAGAGAGGCGTATAAATCC
			AACCCACAAACCTGAGTTGAATTCTGTACAAACTG
			AACCAATGGAAGGTGCTTCTTCAGGGGACAGAAAG
			CAGGAAAATCCCCCAGCTCATTTGGCAAAGCAGTT
			ACCAAATACATTGTCGCGCTCTACAGTGTACTTTGA
			GAAGAAATTTCTTCTGTATTCCCGCAGTTACCAAGA
			ATATTTTCCTAAATCGTTCATACTGAGCCGCCTGCA
			GGGTTGTCAGGCAGGTGGAAGGCGGCTTATAGAAA
			CTATATTCTTAAGCCAAAACCCATTAAAGGAACAG
			CAGAACCAAAGCCTACCACAGCAAAAGTGGCGAA
			AGAAGAGGTTGCCCAAACGCTACTGGCAAATGAGA
			GAGATATTTCAGAAGCTGGTAAAGAACCATGAGAA
			GTGCCCTTATTTAGTTTTCTTGAGGAAAAATTGCCC
			TGTTTTGCTTTCTGAAGCATGTTTGAAAAAGACGGA
			GCTGACCTTGCAGGCGGCTCTGCCTGGGGAAGCAA
			AGGTTCACAAGCACACAGAACATGGGAAAGAGTC
			CACTGAGGGTACTGCACCGAACAGCTTCCTCGCTC
			CTCCCTCAGTGCTAGCGTGTGGGCAGCCAGAGAGA
			GGGGAACAGCACCCTGCAGAGGGGAGTGATCCGCT
			CCTCAGGGAGCTGCTCAGGCAGCACAGCAGCCACT
			GGCAGGTGTATGGCTTTGTGAGGGAGTGCCTGGAG
			CGGGTGATCCCTGCTGAGCTGTGGGGTTCAAGCCA
			TAACAAATGCCGGTTCTTTAAAAACGTGAAAGCAT
			TCATTTCCATGGGGAAGTATGCTAAGCTTTCATTGC
			AGCAGCTGATGTGGAAGATGAGAGTGAATGACTGC
			GTATGGCTTCGTCTGGCCAAAGGTAATCACTCTGTT
			CCTGCCTATGAACATTGTTACCGTGAAGAAATTCTG
			GCAAAATTCCTATACTGGCTGATGGATTCCTATGTT
			ATCGAGTTGCTCAAATCATTTTTCTATATCACCGAG
			ACCATGTTCCAGAAAAACATGCTTTTCTACTACCGA
			AAGTTTATCTGGGGCAAGTTACAGAACATTGGAAT
			TAGAGACCATTTTGCCAAAGTACATCTACGTGCCTT
			GTCTTCAGAGGAGATGGAAGTGATCCGTCAAAAAA
			AGTATTTTCCTATTGCATCAAGGCTCCGGTTCATTC
			CTAAAATGAATGGTTTAAGACCCGTAGTAAGACTA
			AGCCGTGTTGTTGAAGGACAGAAACTCAGCAAGGA
			AAGCAGAGAAAAGAAGATACAGCGCTATAACACT
			CAGCTAAAAAATCTATTTAGTGTTTTAAACTATGAA
			CGAACTGTAAACACCAGTATCATTGGCTCTTCAGT
			ATTCGGGAGAGATGATATCTACAGGAAGTGGAAGG
			AGTTTGTTACAAAGGTTTTTGAATCAGGTGGTGAA
			ATGCCTCATTTCTACTTTGTAAAGGGTGATGTATCC
			AGAGCTTTTGATACCATTCCTCACAAGAAACTTGTG
			GAAGTGATATCACAGGTCTTGAAACCTGAGAGCCA
			AACTGTCTATGGAATAAGGTGGTATGCAGTGATTA
			TGATTACCCCAACTGGAAAAGCCAGGAAACTCTAT
			AAGAGACATGTTTCTACTTTCGAGGATTTTATTCCA
			GACATGAAGCAGTTTGTGTCCAAGCTTCAAGAGAG
			AACTTCATTACGAAATGCAATAGTAGTTGAACAGT
			GCTTAACTTTTAATGAGAACAGTTCCACCCTGTTTA
			CTTTCTTTCTTCAAATGTTACATAATAACATCCTGG
			AGATTGGGCACAGGTACTATATACAGTGCTCTGGA
			ATCCCACAGGGCTCCATTTTGTCAACCTTACTTTGC
			AGCTTATGCTACGGAGACATGGAAAACAAATTACT
			CTGTGGGATCCAGAAGGATGGAGTCCTAATACGTC
			TTATTGATGACTTTTTGCTGGTTACGCCACATTTAA
			TGCAGGCAAGAACTTTTCTAAGGACTATAGCAGCA
			GGTATTCCTGAGTATGGCTTTTTAATAAATGCCAAG
			AAGACTGTGGTGAATTTTCCTGTTGATGATATCCCG
			GGATGTTCCAAGTTCAAACATCTGCCAGATTGTCGT
			TTGATCTCATGGTGTGGTTTATTATTGGATGTGCAG
			ACACTTGAGGTTTATTGTGATTACTCCAGTTATGCC
			TTTACTTCTATCAGATCAAGTCTTTCCTTCAATTCA
			AGTAGAATAGCTGGAAAAAACATGAAATGCAAATT
			GACTGCAGTCCTCAAACTGAAATGCCATCCTTTACT
			TCTTGACTTAAAGATCAACAGCCTTCAGACAGTTCT
			AATTAACATCTACAAGATATTTTTACTTCAGGCTTA
			CAGGTTCCATGCCTGTGTTCTTCAGCTTCCATTCAA
			CCAGAAAGTTAGGAATAATCCTGATTTCTTCCTAA
			GGATCATCTCTGATACTGCTTCATGCTGCTATTTTA
			TCCTGAAAGCTAAAAATCCAGGAGTTTCTTTAGGT
			AGCAAAGATGCATCTGGCATGTTCCCTTTTGAGGC
			AGCAGAATGGCTGTGCTACCATGCCTTCATTGTCA
			AACTGTCCAACCACAAAGTTATTTACAAATGCTTA
			CTTAAGCCCCTTAAAGTCTATAAGATGCATCTGTTT
			GGGAAGATCCCAAGGGATACTATGGAACTGCTGAA
			GACGGTGACGGAACCATCGCTTTGTCAAGATTTCA
			AAACTATACTGGACTAA (SEQ ID NO: 45)
TERT	Turkey	XM_019613879.1	ATGTCTGGGGCTCGGGGGCTCGTCTGGTGCGACGA
	[Meleagris		GCGAGCGTGGCTGTTATCCAGTCAGAGCGAAGTCA
	gallopavo]		TCACAAGAATCGTTCAGAGACTATGTGAAAAGAAA
			AAGAAGAACATCCTTGCGTATGGATACTCCTTGCT
			GGATGAAAACAGTTGTCACTTCAGGATTTTGCCAT
			CTTCGTGCATATACAGCTATCTGCCCAATACTGTAA
			CAGAAACGATTCGCATCAGTGGCCTCTGGGAGATA
			CTGCTGAGCAGGATAGGGGACGATGTGATGATGTA
			CCTGCTGGAGCACTGTGCACTCTTCATGCTGGTTCC
			CCCAAGTAACTGTTACCAGGTCTGCGGGCAACCAA
			TTTATGAACTTATTTCGCGTAACATAGGGCCGTCCC
			CAGGGTTCGTTAGACGACGATATTCAAGGTTTAAA
			CATAATAACTTGCTTAACTATGTGCGAAAAAGACT
			TGTGTTTCATAGGCACTATCTTTCCAAGTCACAGTG
			GTGGAAGTGCGGGCCGAGACGTCAAGGTCGTGTCT
			CCAGCAGAAGAAAAAGAAGGACCCATAGGATACA
			AAGCCCAAGGTCTGGTTACCAGTCTTCTGCAAAAG
			TGAACTTTCAAGCAGGCATGCGGATCAGCACAGTT
			ACTGCACATCTGGAAAAACAGAACTGCTCCAGTTT
			ATGTTTGCCAGCTAGAACACCATCTTTAAAAAGGA
			AGCGTGATGGAGAACAGGTTGAAACCACAGCTAA
			GAGAGTGAAAGTAATGGAGAGAGAGGAACAGGCT
			TGTAGTATCGTTCCTGATGTAAATCGAAGTAGCTCC
			CGGAGGCATGGAGTTTGGCATGTAGCACCACGTGC
			TGTAGGTCTTATTAAAGAACGTTACGTTTCTGAAAG
			AAGTTACAGTGAGATGTCTGGTCCTTCTGTAGTTCA
			CAGATCTCACCCTGGGAAGAGGCCTGTAGCAGACA
			AAAGCTCTTTTCCAAGAGGAGTTCAGGGTAACAAA
			CACATAAAGACCGGTGCAGAAAAACGAGCAGAAT
			CCAATAAAAGGGGCATAGAGATGTATATAAACCCA
			ATCTGTAAACCCAATAGAAGGGGTATAGAGAGGCA
			TATAAATCCAACCCATAAACCTGGGTTGAATTCTGT
			ACAAACTGAACCAATGGAAAGTGCTTCTTCGGGGG
			ACAGAAAGCAGGAAAATCCCCCAGCTCATTTGGCA
			AAGCAGTTACCAAATACATTCTTGCGCTCTGCAGT
			GTACTTTGAGAAGAAATTTCTTCTGTATTCCCGTAG
			TTACCAAGAATATTTTCCTAAATCGTTCATACTGAG
			CCGCCTGCAGGGTTGTCAGGCAGGTGGAAGGCAGC
			TTATAGAAACTATATTTTTAAGCCAAAACCCATTAA
			AGGAAAAGCAGAACCAAAGCCTAAAACAGCAAAA
			GTGGAGAAAGAAGAGGTTGCCCAAACGCTACTGGC
			AAATGAGAGAGATATTTCAGAAGCTGTTAAAAAAC
			CACGAGAAGTGCCCTTATTTAGTTTTCTTGAGAAAA
			AATTGCCCTGTTTTGCTTTCTGAAGCATGTTTGAAA
			AAAACGGAGCTGACCTTGCAGGCAGCTCTGCCTGG
			GGAAGCAAAGGTTCACAAGCACACAGAACATGGG
			GAAGAGACCACTGAGGGTACTGCACCGAACAGCTT
			CTACACTCCTCCCTCAATGCCATTGTGTGGGCAGAC
			AGAGAGAGAGGAGCAGCACCTTGCAGAGGGGAGT
			GATCCGCTCCTCAGGGAGCTGCTCAGGCAGCACAG
			CAGCCACTGGCAGGTGTATGGCTTTGTGAGGGAGT
			GCCTGGAGCGGGTGATTCCTGCCGAGCTGTGGGGT
			TCAAGCCATAACAAATGCCGGTTCTTTAAAAACGT
			GAAAGCATTCATTTCCATGGGGAAGTATGCTAAGC
			TTTCATTGCAGCAGCTGATGTGGAAGATGAGAGTG
			AATGACTGCGTATGGCTTCGTCTGGCCAAAGGTAA
			TCATTCTGTTCCTGCCTATGAACATTGTTACCGTGA
			AGAAATTTTGGCAAAATTCCTATACTGGCTGATGG
			ATTCCTATGTTATCGAGTTGCTCAAATCATTTTTCT
			ATATCACCGAGACCATGTTCCAGAAAAACATGCTT
			TTCTACTACCGAAAGTTTATCTGGGGCAAGTTACA
			GAACATTGGAATTAGAAACCATTTTGCCAAAGTAC
			ATCTACGTGCTTTATCTTCAGAGGAGATGGAAGTG
			ATCCATCAAAAAAAGTATTTTCCTATTGCATCAAG
			GCTCCGGTTCATTCCTAAAATCAATGGTTTAAGACC
			CGTAGTAAGACTAAGCCGTGTTGTTGAAGGACAGA
			AACTCAGCAAGGAAAGCAGAGAAAAGAAGATACA
			GCGCTATAACACTCAGCTAAAAAATCTATTTAGTG
			TGTTAAATTATGAACGAACTGTAAACACCAGTATC
			ATTGGCTCTTCAGTATTCGGGAGAGATGATATCTAC
			AGGAAGTGGAAGGAGTTTGTTACAAAGGTTTTTGA
			ATCAGGTGGTGAAATGCCTCATTTCTACTTTGTGAA
			GGGTGATGTGTCCAGAGCTTTTGATACTATTCCTCA
			CAAGAAACTTGTGGAAGTGATCTCACAGGTCTTGA
			AACCTGAGAGCCAAACTGTATATGGAATAAGGTGG
			TATGCTGTGATTATGATTACCCCAACTGGAAAAGC
			CAGGAAGCTCTATAAGAGACACGTTTCTACTTTTG
			AGGATTTTATTCCAGACATGAAGCAGTTTGTGTCCA
			AGCTTCAAGAGAGAACTTCATTACGAAATGCAATA
			GTAGTTGAACAGTGCTTAACTTTTAATGAGAACAG
			TTCCACCCTGTTTACTTTCTTTCTTCAAATGTTACAT
			AATAACATCCTGGAGATTGGGCACAGGTACTATAT
			ACAGTGCTCTGGAATCCCACAGGGCTCCATTTTGTC
			AACCTTACTTTGCAGCTTATGCTATGGAGACATGG
			AAAACAAATTACTTTGTGGAATCCAGAAGGATGGA
			ATCCTAATACGTCTTATTGATGACTTTTTGCTGGTT
			ACACCACATTTAATGCAGGCAAAAACTTTTCTAAG
			GACTATAGCAGCAGGTATTCCTGAGTATGGCTTTTT
			AATAAATGCCAAGAAGACAGTGGTGAATTTTCCTG
			TTGATGATATTCCGGGATGTTCTAAGTTCAAACAGC
			TGCCAGATTGTCGTTTGATCTCATGGTGCGGTTTAT
			TACTGGATATGCAGACACTTGAGGTTTATTGTGATT
			ACTCCAGTTATGCCTTTACTTCTATCAGATCAAGTC
			TTTCCTTCAATTCAAGTAGAATAGCTGGAAAAAAC
			ATGAAATGCAAATTGACTGCAGTCCTCAAACTGAA
			ATGCCATCCTTTATTTCTTGACTTAAAGATCAACAG
			CCTTAAAACAGTTTTAATTAACATCTACAAGATATT
			TTTACTTCAGGCTTACAGATTCCATGCCTGTGTTCT
			TCAGCTTCCATTCAACCAGAAAGTTAGGAATAATC
			CTTATTTCTTTGTAAGGATCATCTCTGATACTGCTT
			CATGCTGCTATTTTATCCTGAAAGCTAAAAATCCAG
			GGGTTTGTTTAGGTTGCAAAGATGCATCTGGCATGT
			TCCCTTTTGAGGCAGCAGAATGGCTCTGCTACCATG
			CTTTCATTGTCAAACTGTCCAACCACAAAGTTATTT
			ACAAATGCTTACTTAAGCCCCTTAAAGTCTATAAG
			ATGCATCTGTTTGGGAAGATACCAAGGGATACTAT
			GGTACTGCTGAAGACAGTGACGGAACCATCTCTTT
			GTCAAGATTTCAAAACTATACTGGACTAA (SEQ ID
			NO: 46)
TERT	Duck	XM_013104503.2	ATGCAGAGGCTGTGTGGGAAAAAGAAGAAGAACA
	[Anas		TCCTCACGTATGGATACTCCTTGCTGGATGAAAAC
	platyrhynchos]		AGTTCTCACTTCCAAATCATGCCGCTCTCAAACGTG
			TACAGCTACCTGCCCAACACCGCAACAGAAACCAT
			GCGTATCAGTGGCCTCTGGGAAACGCTGCTGAGCA
			GGATAGGGGATGACGTGATGATGTATTTATTGGAA
			CACTGTGCGATCTTTATGCTGGTTCCCCCTAGTAAC
			TGTTACCAAGTCTGTGGGCAACCAATTTATGAACTT
			ATTTCGCAAAATGTAGAATCAGCCCCAGCGTTTGTT
			AAACAACGGCTTTCAAAGCACAAACGTAGTAGCTT
			GCTTAAGTATACCCAGAAAAGGCTAACGTTTCACA
			GACAGTATCTTTCAAAGTCACGTCAGTCGAAACGC
			AGGCAAAGACTTGAAGCTAATGTCTCCAGCGTGAG
			AAATAAAACCAGCAATAATATACAAAGCCTAGGGT
			CCGCTGCTCTGGAAAAACAGAGTAGCTCCAATGCA
			GGTTTGTCAGCTACAGCACCGTCCTTAAAAAGGAA
			GCTTGCTAGGGAGCAACTGGAAGTCACGGCTAAGA
			GAGCAAGATTAGAAGAGAAAGAGAGGGAGGAACA
			GGCATGTAATACTGCTCCTAATGTAAACCAGAGCA
			TTCCCAAGAGGTATGGAACCGGCTGTGTAGCATCA
			CGTTCTGTAAGTCTGACTAAAGAAAAAAACATTTC
			TCAAAGAAGTAACAGTGATATGCCTCGTCCTTCTTT
			AGTTCACAATTCTCATCGCGGGAAGAAGTCTGTGG
			CAGACAAAAGCTCTTTCCTGCAAGGAGCTGAGAGT
			AACAGACATTTAAAGCCCAGCATTGAAATGCAAGC
			AGGATCCAGCAGGAAGGGAGTGGAGACACGCAGG
			CCTATACCTCGGTTGGATTGGGTACCAATCGAACC
			GGCGGAAAGTAGTTCTTCAGGACACAAAAAGCAG
			GAAGGTCCCCTAGCTCATCTGGCAGAGGAGGTACC
			AAATAGGGTTTTGCCATCTACAATATACATTGACA
			GGAAGTTTCTGTATTCTCGCAGATACTGGGGGGAG
			CGTTTCCCGAAATCCTTCCTATTGAATCGCCTGAAG
			GGTAGCCAGGCAGGTGTAAAGCGGCTAATAGAAA
			CGATATTCTTAAGCCAAAATCCGTTTGGGCAAAAG
			TGCAACCAAGGTCTGCCACAGAAAAAACGGAGAA
			AGAAGAAGCTTCCCAAACGCTTCTGGAGAATGAGA
			AGTATATTTCAACAACTCTTAAAGAATCATGGAAA
			GTTCCCTTACGTAGCTTTCTTGAGACAAAATTGCCC
			TCTTCGGATATCTGACACCATTTTGGGAAAAGCCA
			AGCTGCTCAGTCGGGCACCTTTGCCTGGGCAAGCA
			GAGGCTCGCAAGCAAGCAGAACAGCTTGGGAAGG
			AGCCTGCTGAGCGTGTGGCAAGCAGCAGATGTGAA
			TCTGGTCACACCAACGTGCCCAGCAGCGTACGCGC
			TCCTCTCGCAGCATCTGCGTGTGGGGAGCCGGGGG
			GTGAGGAGCAGATCCCTGCAGAGGCGTCTGATTCA
			GTCCTCAGGGAGCTTCTCAAGGAGCACTGCAGCCA
			CTTCCAGGTGTACCTCTTTGTGAGGGAGTGCGTGG
			AGAGGGTGATCCCCACCGAGCTCTGGGGTTCAAAC
			CATAACAAGCGCCGGTTCTTCAAGAACGTGAAAGC
			GTTCATTTCCATGGGGAAGTACGCTAAGCTTTCCTT
			GCAGGTGTTGATGTGGAAGATGAGAGTAAATGACT
			GCATGTGGCTTCGTCTGGCCAAAGGTAATCACTTTG
			TTCCTGCCTCTGAACACCTTTACCGTGAAGAAATTT
			TGGCTAAATTCCTATACTGGCTGATGGATACGTATG
			TTGTTCAGTTGCTCAGATCATTTTTCTATGTCACCG
			AGACCATGTTCCAGAAAAACATGCTCTTCTACTAC
			CGAAAGTGTATTTGGGGCAAGTTACAGGACATTGG
			AATTAGAAAGCATTTTTCCAAAGTGAAGCTACGTC
			CTTTAACTGCAGAGGAGATGGAAGCGATCCATCAA
			AAAAAATACCTTCCTATGGCGTCAAAGCTCCGTTTC
			ATTCCCAAAGTCACTGGACTAAGACCCATCGTCAG
			AATGAGCGGTGTTGTTGAAGCACAAACGTTGAGCA
			AGGAAAGCAGAGCAAAGAAGGCCGATGTGTCCAG
			GGCTTTTGATAGCATTCCTCACAATAAACTTGTGGA
			AGTGATTTCACAGGTCTTAAAACCCGAGAAAAAAA
			CTGTCTACTGCATACGGCGCTATGCAGTGGTTATGA
			TCACTGGAAGTGGAAAAACCAGGAAGTTATATAAG
			AGACATGTTTCTACTTTCAAGGATTTTATGCCAGAC
			ATGAAGCAGTTTGTGTCCCGGCTTCATGAGAGTAC
			CTCATTGCGAGATGCAATAATAGTTGAACAGAGCC
			TAACTTTCAATGAGACAAGTGCCAGTCTATTTAATT
			TTTTTCTTCAAATGCTAAATAATAACATCCTGGAAA
			TTGAGCGCAGTTACTACTTACAGTGCTCTGGAATTC
			CACAGGGCTCCCTTTTGTCAACCTTGCTTTGCAGCT
			TGTGCTATGGAGACATGGAAAACAAATTATTCAGT
			GGGGTACAGAAGGATGGAGTCCTGATCCGTCTCAT
			TGATGACTTTTTGCTGGTTACACCACATTTAATGCA
			TGCAAGAACTTTTCTAAGGACTCTAGCAATGGGCA
			TTCCTGAGTATGGCTTTTTGATAAACCCCAAAAAG
			ACAGTGGTGAATTTTTCTGCTGACGATATCCCAGA
			ATGTTCTGAATTTAAACAGCTGCCAAACTGTCGTTT
			GATCCCATGGTGTGGCTTATTATTGGATACACAGA
			CACTTGAGGTTTACTGCGATTACTCCAGCTATTCCT
			GTACTTCTATCAGATCAAGTCTTTCCTTCAATTCAA
			ACAGAACAGCTGGGAAAAACATGAAACACAAATT
			GCTTGCAGTCCTTAAACTGAAATGCCATGGCTTGTT
			TCTCGATTTACAGATCAATAGCCTTAAAACAGTTTT
			CATTAACGTCTACAAGATATTTTTACTTCAGGCTTA
			CAGGTTCCATGCCTGTGTTATTCAACTTCCATTCAA
			CCAGAAAGTTAGGAACAATCCTGATTTCTTCCTCA
			GAGTCATCGCTGAGAATGCATCGTGCTGCTATTCTA
			TGCTAAAAGCTAAAAATCCAGGGTTTACTTTAGGT
			AACAGAGGTGCATCTGGCATGTTTCCTTCTGAGGC
			AGCAGAGTGGCTCTGCTATCATGCCTTCACTGTCAA
			ACTGTCAAACCACAAAGTTGTTTACAAATGCTTGCT
			GAAGCCCCTGAAGTTCTGTATGATGCAGCTATTCC
			GGAAGATCCCAAAGGATACTAAGGCACTACTGAAG
			ACAGTGACAGAACCATCTATTTGTAAAGATTTCAA
			ATCTATCCTGGACTGA (SEQ ID NO: 47)

TABLE 1C
Gene	Species	NCBI #	Amino Acid Sequence
IGF2	Cow [Bos	NP_776512.2	MGITAGKSVLVLLAFLAFASCCYAAYRPSE
	Taurus]		TLCGGELVDTLQFVCGDRGFYFSRPSSRINR
			RSRGIVEECCFRSCDLALLETYCATPAKSER
			DVSASTTVLPDDVTAYPVGKFFQYDIWKQ
			STQRLRRGLPAFLRARRGRTLAKELEALRE
			AKSHRPLIALPTQDPATHGGASSKASSD
			(SEQ ID NO: 26)
IGF1	Zebrafish	NP_571900.1	MSSGHFFQGHWCDVFKCTMRCLPSTHTLS
	[Danio rerio]		LVLCVLALTPATLEAGPETLCGAELVDTLQ
			FVCGDRGFYFSKPTGYGPSSRRSHNRGIVD
			ECCFQSCELRRLEMYCAPVKTGKSPRSLRA
			QRHTDIPRTPKKPISGHSHSSCKEVHQKNSS
			RGNTGGRNYRM (SEQ ID NO: 27)
serum	Rainbow trout	XP_021470329.1	MRRPCILAIQPDTEFMPPELDASNFHMGPEL
albumin	[Oncorhynchus		CTKDSKELLLSGKKLLYGVVRHKTTITEEQ
1	mykiss]		LKSISTKYHSMKEKCCAAEDQAACFTEEAP
			KLVAESAELVKA (SEQ ID NO: 28)
GLUL	Tilapia	NP_001266597.1	MATSASASLSKAVKQQYMELPQGDKVQA
	[Oreochromis		MYIWIDGTGEGLRCKTRTLDSEPKSIEDLPE
	niloticus]		WNFDGSSTYQSEGSNSDMYLIPSAMFRDPF
			RKDPNKLVLCEVLKYNRKPTETNLRLTCK
			KVMDMVADQHPWFGMEQEYTILGTDGHP
			FGWPSNGFPGPQGPYYCGVGADKAYGRD
			VVEAHYKACLYAGVQICGTNAEVMPAQW
			EFQVGPCEGIDMGDHLWVARFILHRVCEDF
			GVVASFDPKPIPGNWNGAGCHTNFSTKEM
			REDGGLKAIEDSIEKLGKRHSYHIRAYDPK
			GGLDNARRLTGRHETSNINEFSAGVANRG
			ASIRIPRNVGQEKKGYFEDRRPSANCDPYS
			VTEALIRTCLLNEEGDEPADY (SEQ ID NO:
			29)
IGF2	Rainbow trout	NP_001118169.1	METQKRHEYHSVCHTCRRTENTRMKVKM
	[Oncorhynchus		MSSSNRVLVIALALTLYIVEVASAETLCGG
	mykiss]		ELVDALQFVCEDRGFYFSRPTSRSNSRRSQ
			NRGIVEECCFRSCDLNLLEQYCAKPAKSER
			DVSATSLQIIPMVPTIKQDVPRKHVTVKYS
			KYEAWQRKAAQRLRRGVPAILRARKFRRQ
			AVKIKAQEQAMFHRPLITLPSKLPPVLPPTD
			NYVSHN (SEQ ID NO: 30)
IGF1	Tropical	XP_002936875.1	MEKNNSLSTQLFKCYFCDFLKLKMHKMSY
	clawed frog		IHLLYLALCFLTLTHSAAAGPETLCGAELV
	[Xenopus		DTLQFVCGDRGFYFSKPTGYGSSNRRSHHR
	tropicalis]		GIVDECCFQSCDFRRLEMYCAPAKPAKSAR
			SVRAQRHTDMPKAQKEVHLKNASRGNTGS
			RGFRM (SEQ ID NO: 31)
GLUL	Tropical	XP_004914095.1	MATSASAQLSKAIKQMYLELPQGDKVQAM
	clawed frog		YIWVDGTGEGLRCKTRTLDSEPKTIEDLPE
	[Xenopus		WNFDGSSTYQSEGSNSDMYLIPVAMFRDPF
	tropicalis]		RRDPNKLVLCEVLKYNRKTAETNLRHTCN
			QIMDMMANEHPWFGMEQEYTLLGMDGHP
			FGWPSNGFPGPQGPYYCGVGADKAYGRDI
			VEAHYRACLYAGVKIAGTNAEVMPAQWE
			FQIGPCEGIEMGDHLWIARFILHRICEDFGII
			VSFDPKPITGNWNGAGCHTNFSTKSMREEG
			GLKDIEESIERLSKRHDYHIRMYDPRGGKD
			NARRLTGFHETSSIHEFSAGVANRGASIRIP
			RSVGQEKKGYFEDRRPSANCDPYAVTEAM
			IRTCLLNETGDEPLEYKN (SEQ ID NO: 32)
ALB	Tropical	AAH75287.1	MNALMRRACCGALFPLSFRLAALSPMKGA
	clawed frog		SNFSCGNVCASPAGCWAPPSGHDTGIKVY
	[Xenopus		NSLTRRKDPLILADPTVATWYSCGPTVYDH
	tropicalis]		AHLGHACSYVRFDIIRRILLKVFGIDTVVVM
			VVTDIDDKIIKRAKELNISPVALARTYEQDF
			KQDMTALKVLPPTVYMRVTENIPQIISFIEHI
			IANGYAYATSQGNVYFDVQSIGERYGKFN
			DSFSDTASESASQDKRHIRDFALWKTSKPE
			EPYWASPWGKGRPGWHIECSTIASSVFGKH
			LDIHTGGIDLAFPHHENEIAQCEAYHQSTQ
			WGNYFLHTGHLHLKGNEEKMSKSLRNYLT
			VKEFLKSFSPDQFRMFCLRSKYKSAVEYSN
			GSMHDAVNTLHTISSFVDDAKAYMKGQLI
			CQPVQEALLWQRLNETKVNVKAAFSDDFD
			TPRAVDAVMDLIHHGNRQLKAVSKESNSP
			RSSVVYGAMISYIEQFLEILGISLSQNQVAA
			EDRHSAVLFNVVEEMISFRSKVRNYALAA
			DESPNAIGQEEKQQYKERRRQLLLEREPLL
			QACDIMRQHLAVYGINVKDRGNTSTWELL
			DRKEET (SEQ ID NO: 33)
IGF2	Tropical	NP_001107144.1	MRHLLLLSITFLVYTLDSAKAYGATETLCG
	clawed frog		GELVDTLQFVCGDRGFYFSRNNGRSNRRA
	[Xenopus		NRGIVEECCFRSCDLELLETYCAKPAKNER
	tropicalis]		DVSTAPSTAIPPLNKQDLYHKHHHTKSSKY
			DIWQRKSIHRLRRGVPAIVRARQYRLLMQQ
			AEESEQALSHRPLTTLPITRPLHLQQTSEPSL
			N (SEQ ID NO: 34)
GLUL	Chicken	NP_990824.1	MATSASSHLSKAIKHMYMKLPQGEKVQA
	[Gallus gallus]		MYIWIDGTGEHLRCKTRTLDHEPKSLEDLP
			EWNFDGSSTFQAEGSNSDMYLRPAAMFRD
			PFRKDPNKLVLCEVFKYNRQSADTNLRHT
			CRRIMDMVSNQHPWFGMEQEYTLLGTDG
			HPFGWPSNCFPGPQGPYYCGVGADKAYGR
			DIVEAHYRACLYAGVKIGGTNAEVMPAQW
			EFQVGPCEGIEMGDHLWIARFILHRVCEDF
			GVIVSFDPKPIPGNWNGAGCHTNFSTKNMR
			EDGGLKHIEEAIEKLSKRHQYHIRAYDPKG
			GLDNARRLTGFHETSSIHEFSAGVANRGASI
			RIPRNVGHEKKGYFEDRGPSANCDPYAVTE
			ALVRTCLLNETGDEPFEYKN (SEQ ID NO:
			35)
ALB	Chicken	NP_990592.2	MKWVTLISFIFLFSSATSRNLQRFARDAEHK
	[Gallus gallus]		SEIAHRYNDLKEETFKAVAMITFAQYLQRC
			SYEGLSKLVKDVVDLAQKCVANEDAPECS
			KPLPSIILDEICQVEKLRDSYGAMADCCSKA
			DPERNECFLSFKVSQPDFVQPYQRPASDVIC
			QEYQDNRVSFLGHFIYSVARRHPFLYAPAIL
			SFAVDFEHALQSCCKESDVGACLDTKEIVM
			REKAKGVSVKQQYFCGILKQFGDRVFQAR
			QLIYLSQKYPKAPFSEVSKFVHDSIGVHKEC
			CEGDMVECMDDMARMMSNLCSQQDVFSG
			KIKDCCEKPIVERSQCIMEAEFDEKPADLPS
			LVEKYIEDKEVCKSFEAGHDAFMAEFVYE
			YSRRHPEFSIQLIMRIAKGYESLLEKCCKTD
			NPAECYANAQEQLNQHIKETQDVVKTNCD
			LLHDHGEADFLKSILIRYTKKMPQVPTDLL
			LETGKKMTTIGTKCCQLPEDRRMACSEGY
			LSIVIHDTCRKQETTPINDNVSQCCSSSYAN
			RRPCFTAMGVDTKYVPPPFNPDMFSFDEKL
			CSAPAEEREVGQMKLLINLIKRKPQMTEEQ
			IKTIADGFTAMVDKCCKQSDINTCFGEEGA
			NLIVQSRATLGIGA (SEQ ID NO: 36)
IGF1	Chicken	NP_001004384.1	MEKINSLSTQLVKCCFCDFLKVKMHTVSYI
	[Gallus gallus]		HFFYLGLCLLTLTSSAAAGPETLCGAELVD
			ALQFVCGDRGFYFSKPTGYGSSSRRLHHKG
			IVDECCFQSCDLRRLEMYCAPIKPPKSARSV
			RAQRHTDMPKAQKEVHLKNTSRGNTGNR
			NYRM (SEQ ID NO: 37)
IGF2	Chicken	NP_001025513	MCAARQILLLLLAFLAYALDSAAAYGTAE
	[Gallus gallus]		TLCGGELVDTLQFVCGDRGFYFSRPVGRN
			NRRINRGIVEECCFRSCDLALLETYCAKSV
			KSERDLSATSLAGLPALNKESFQKPSHAKY
			SKYNVWQKKSSQRLQREVPGILRARRYRW
			QAEGLQAAEEARAMHRPLISLPSQRPPAPR
			ASPEATGPQE (SEQ ID NO: 38)

Provided herein are expression vectors comprising any one of the sequences selected from Tables 1A and 1B, and cells comprising any one of such expression vectors, for example a cell is from a livestock, poultry, game, or aquatic species.

Exemplary Methods and Compositions

Provided herein are methods of increasing the efficiency of maintaining cells in culture.

In some embodiments, provided herein is a method of decreasing the concentration of ammonia in the culture medium of cells comprising increasing the expression of glutamine synthetase (GS) protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of ammonia in the culture medium is decreased by at least 2.5%.

In some embodiments, provided herein is a method of increasing the production of glutamine in cells comprising increasing the expression of glutamine synthetase (GS) protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of glutamine in the cells is increased by at least 2.5%.

In some embodiments, provided herein is a method of increasing the concentration of Insulin-like growth factor (IGF) in the medium of cells in culture comprising increasing the expression of IGF protein secreted by the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of IGF in the ambient medium, or within the cell, is increased by at least 2.5%.

In some embodiments, provided herein is a method of increasing the concentration of albumin in the medium of cells in culture comprising increasing the expression of albumin in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of albumin in the ambient medium, or within the cell, is increased by increased by at least 2.5%.

In some embodiments, provided herein are methods for increasing the cell density of a culture comprising metazoan cells comprising introducing any combination of the following cellular modifications: increased expression of GS, increased expression of IGF, increased expression of albumin, increased expression of telomerase reverse transcriptase (TERT), loss-of-function mutations in cyclin-dependent kinase inhibitor (CKI) proteins, increased expression of YAP, increased expression of TAZ, increased expression of myogenic transcription factors.

In some embodiments, provided herein is a method for increasing the cell density of a culture comprising metazoan cells, the method comprising (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), and albumin; and (b) culturing the cells in a cultivation infrastructure.

In some embodiments, provided herein is a method for increasing the cell density of a culture comprising metazoan cells, the method comprising (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or combinations (GS+IGF; GS+albumin; IGF+albumin; GS+IGF+albumin) thereof; and (b) culturing the cells in a cultivation infrastructure.

In some embodiments, provided herein is a method for increasing the cell density of a culture comprising metazoan cells, the method comprising (a) introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or combinations (GS+IGF; GS+albumin; IGF+albumin; GS+IGF+albumin) thereof; (b) introducing into the cells a polynucleotide sequence encoding a telomerase reverse transcriptase (TERT); and (c) culturing the cells expressing GS, IGF, albumin or combinations thereof and TERT in a cultivation infrastructure.

As provided herein, the density of cells in a culture or cultivation infrastructure is determined by calculating the cell number per unit volume of the cultivation infrastructure, by determining the biomass per unit volume of the cultivation infrastructure, by determining the biomass DNA content per unit volume of the cultivation infrastructure, by determining the biomass RNA content per unit volume of the cultivation infrastructure, by determining the biomass protein content per unit volume of the cultivation infrastructure, or by visual, electronic, metabolic, spectroscopic, or microscopic, measurement of the biomass density.

In some embodiments, an increase in the cell density of a culture using the methods described herein is about 1.025 fold, 1.05 fold, 1.10-fold, 1.15-fold, 1.20-fold, 1.25-fold, 1.30 fold, 1.35-fold, 1.40-fold, 1.45-fold, 1.5-fold, 2-fold, 2.5-fold, 3-fold, 3.5-fold, 4-fold, 4.5-fold, 5-fold, 7.5-fold, 10-fold, 15-fold, 20-fold, 25-fold, 30-fold, 40-fold, or even about 50-fold, 75-fold, 100-fold, 150-fold, or is even about 200-fold, compared to the density of a culture comprising cells that do not include one or more cellular modifications described herein.

In some embodiments, an increase in the density of cells in a culture using the methods described herein is at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100%, at least 150%, at least 200%, at least 250%, at least 300%, at least 350%, at least 400%, at least 450%, at least 500%, at least 550%, at least 600%, at least 650%, at least 700%, at least 750%, at least 800%, at least 850%, at least 900%, at least 950%, at least 1000%, compared to the cell density of a culture comprising cells that do not include one or more cellular modifications described herein.

In some embodiments, using the methods described herein, there is an increased yield of cellular biomass harvestable per unit volume of the cultivation infrastructure. In some embodiments, the increase is at least about 1.0-fold, 1.25-fold, 1.5-fold, 2-fold, 2.5-fold, 3-fold, 3.5-fold, 4-fold, 4.5-fold, 5-fold, 7.5-fold, 10-fold, 15-fold, 20-fold, 25-fold, 30-fold, 40-fold, or even about 50-fold, 75-fold, 100-fold, 150-fold, or is even about 200-fold compared to the yield of cellular biomass harvestable per unit volume of the cultivation infrastructure in the absence of one or more cellular modifications described herein.

In some embodiments, methods described herein increase the density of cells in a culture by increasing the rate of proliferation of cells in the culture. In some embodiments, the increase in the rate of cell proliferation is at least 2.5%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100%, at least 150%, at least 200%, at least 250%, at least 300%, at least 350%, at least 400%, at least 450%, at least 500%, at least 550%, at least 600%, at least 650%, at least 700%, at least 750%, at least 800%, at least 850%, at least 900%, at least 950%, or at least 1000%, including values and ranges therebetween, compared to the rate of proliferation of cells that do not include one or more cellular modifications described herein. In some embodiments, the increase in the rate of cell proliferation is about 25-1000%, about 25-750%, about 25-500%, about 50-1000%, about 50-750%, about 50-500%, about 100-1000%, about 100-750%, or about 100-500%, including values and ranges therebetween, compared to the rate of proliferation of cells that do not include one or more cellular modifications described herein.

In some embodiments, methods described herein increase the cell density of a culture by decreasing cell death within the cellular biomass. In some embodiments, the decrease in cell death is at least 2.5%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100%, including values and ranges therebetween, compared to the rate of cell death in cells that do not include one or more cellular modifications described herein. In some embodiments, a decrease in the rate of cell death within the cellular biomass is about 2.5-10%, about 2.5-75%, about 2.5-50%, about 5.0-100%, about 5.0-75%, about 5.0-50%, about 10-100%, about 10-75%, or about 10-50%, including values and ranges therebetween, compared to the rate of cell death in cells that do not include one or more cellular modifications described herein.

In some embodiments, using the methods described herein, the density of cells in a culture may reach about 10⁵ cells/mL, about 10⁶ cells/mL, about 10⁷ cells/mL, about 10⁸ cells/mL, about 10⁹ cells/mL, or about 10¹⁰ cells/mL (cells in the cellular biomass/mL of cultivation infrastructure), including values and ranges therebetween.

In some embodiments, using the methods described herein, the density of cells in a culture may reach about 1 g/L, 5 g/L, 10 g/L, 25 g/L, 50 g/L, 75 g/L, 100 g/L, 150 g/L, 200 g/L, 250 g/L, 300 g/L, 350 g/L, 400 g/L, 450 g/L, 500 g/L, 550 g/L, 600 g/L, 650 g/L, 700 g/L, 750 g/L, 800 g/L, 850 g/L, 900 g/L, or 1000 g/L (g of cellular biomass/L of cultivation infrastructure), including values and ranges therebetween. In some embodiments, the density of cells in a culture may range from about 1 g/L to about 5 g/L, about 1 g/L to about 750 g/L, about 1 g/L to about 500 g/L, about 1 g/L to about 250 g/L, about 1 g/L to about 100 g/L, about 1 g/L to about 50 g/L, about 5 g/L to about 1000 g/L, about 5 g/L to about 750 g/L, about 5 g/L to about 500 g/L, about 5 g/L to about 250 g/L, about 5 g/L to about 100 g/L, about 5 g/L to about 50 g/L, about 25 g/L to about 1000 g/L, about 25 g/L to about 750 g/L, about 25 g/L to about 500 g/L, about 25 g/L to about 300 g/L, about 25 g/L to about 250 g/L, about 25 g/L to about 100 g/L, about 50 g/L to about 1000 g/L, about 50 g/L to about 750 g/L, about 50 g/L to about 500 g/L, about 50 g/L to about 300 g/L, about 50 g/L to about 250 g/L, about 100 g/L to 1000 g/L, about 100 g/L to about 750 g/L, about 100 g/L to about 500 g/L, about 200 g/L to about 1000 g/L, about 200 g/L to about 750 g/L, about 200 g/L to about 500 g/L, about 300 g/L to about 1000 g/L, about 300 g/L to about 800 g/L, about 400 g/L to about 1000 g/L, or about 500 g/L to about 1000 g/L including values and ranges therebetween.

In some embodiments, provided herein is an in vitro method for producing a cultured edible product (e.g. cultured poultry, cultured livestock, cultured game, cultured fish), the method comprising: (a) introducing one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or combinations (GS+IGF; GS+albumin; IGF+albumin; GS+IGF+albumin) thereof into myogenic metazoan cells; (b) optionally introducing a polynucleotide sequence encoding a telomerase reverse transcriptase (TERT) into the myogenic metazoan cells; (c) inducing myogenic differentiation of the cells, wherein the differentiated cells form myocytes and multinucleated myotubes; and (d) culturing the myocytes and myotubes to generate skeletal muscle fibers, thereby producing a cultured edible product. In one embodiment, myogenic cells are natively myogenic. In another embodiment, myogenic cells are not natively myogenic and are modified to become myogenic cells by expressing one or more myogenic transcription factors.

In some embodiments, provided herein is an in vitro method for producing a cultured edible product, the method comprising: (a) overexpressing GS, IGF, albumin, or a combination thereof in a self-renewing cell line, wherein the cell line is a myogenic transcription factor-modified cell line, and wherein the cell line is of a livestock, poultry, game or aquatic animal species; (b) inducing myogenic differentiation of the cell line, wherein the differentiated cell line forms myocytes and multinucleated myotubes; and (c) culturing the myocytes and myotubes to generate skeletal muscle fibers, thereby producing a cultured edible product. In some embodiments, provided herein is cultured edible product produced by the in vitro methods.

In the methods for producing a cultured edible product provided herein, myogenic differentiation can be induced in a variety of ways. In some embodiments, cellular biomass with increased cell density can be differentiated into a phenotype of interest by contacting the cells with a differentiation agent. For example, if the phenotype of interest for the expanded cellular biomass is skeletal muscle and the cellular biomass comprises non-myogenic cells (e.g., non-myogenic stem cells or fibroblasts), the expanded cellular biomass can be contacted with a differentiation agent that would induce the skeletal muscle phenotype into the cells of the biomass. Exemplary differentiation agents that may induce skeletal muscle phenotype include myogenic transcription factors such as MYOD1, MYOG, MYF5, MYF6, PAX3, PAX7, paralogs, orthologs, and genetic variants thereof. A PCT publication, WO/2015/066377, discloses exemplary methods for differentiating cells into a skeletal muscle phenotype and is incorporated by reference herein in its entirety. Accordingly, in some embodiments, the expanded cellular biomass may be differentiated into the skeletal muscle phenotype using the methods described in WO/2015/066377.

In some embodiments, cells of the expanded biomass can be differentiated into a phenotype of interest without a differentiation agent. For example, if the phenotype of interest for the expanded biomass is a skeletal muscle and the cellular biomass comprises cells of the skeletal muscle lineage, then these cells may differentiate into the skeletal muscle phenotype on their own without a need for an external differentiation agent. However, in some embodiments, an external differentiation agent such as one or more myogenic transcription factors can be used to differentiate cells of the skeletal muscle lineage into the skeletal muscle phenotype.

Induction of myogenic differentiation in cells overexpressing any one of the cellular modifications described herein would result in the formation of differentiated myocytes and multinucleated myotubes. These myocytes and myotubes are cultured to generate skeletal muscle fibers thereby producing a cultured edible biomass or a cultured edible product.

The cultured edible biomass/product can be processed as a raw, uncooked edible product (cultured meat) or as a cooked edible product or as a cooked/uncooked food ingredient. In some embodiments, processing comprises withdrawal of the culture medium that supports the viability, survival, growth, expansion and differentiation of the cellular biomass. Withdrawal may comprise physical removal of the culture medium or altering the composition of the culture medium, for example, by addition of components that would reduce or prevent further expansion and/or differentiation of the biomass or by depletion of components that support expansion and/or differentiation of the biomass.

In some embodiments, processing comprises exposing the cultured edible biomass to sub-physiological temperatures that would not support the expansion and/or differentiation of the biomass. Sub-physiological temperatures include a temperature of about 15° C. (about 59° F.) or lower, about 10° C. (about 50° F.) or lower, about 0° C. to about 15° C. (about 32° F. to about 59° F.), about 0° C. to −15° C. (about 32° F. to about 5° F.), about −15° C. to about 15° C. (about 5° F. to about 59° F.), about 0° C. to −213° C. (about 32° F. to about −350° F.), about −30° C. to about −100° C. (about −22° F. to about −148° F.), about −50° C. to about −90° C. (about −58° F. to about −130° F.), or about −170° C. to about −190° C. (about −274° F. to about −310° F.). For example, in one embodiment, the expanded and/or differentiated biomass can be cooled to a temperature of about 2° C. to about 8° C. (about 35° F. to about 46.5° F.). In another embodiment, the expanded and/or differentiated biomass can be frozen, for example, by cooling to a temperature of about 32° F. or lower, e.g. about 32° F. to about 0° F., about 32° F. to about −10° F., about 32° F. to about −20° F., about 32° F. to about −30° F., about 32° F. to about −40° F., about 32° F. to about −50° F., about 32° F. to about −60° F., about 32° F. to about −70° F., about 32° F. to about −80° F., and the like. In some embodiments, the expanded and/or differentiated biomass can be exposed to sub-physiological temperatures as low as about −300° F. to about −350° F., such as the liquid nitrogen temperature of about −321° F.

In some embodiments, processing comprises exposing the biomass to superphysological temperatures that would not support the viability, survival, expansion and/or differentiation of the biomass. In one embodiment, exposing the biomass to superphysiological temperatures comprises fully or partially cooking the biomass, for example, by heating the biomass to a temperature of about 100° F. to about 600° F., about 100° F. to about 550° F., about 100° F. to about 500° F., about 100° F. to about 450° F., about 100° F. to about 400° F., about 100° F. to about 350° F., about 100° F. to about 300° F., about 100° F. to about 250° F., about 100° F. to about 200° F. or about 100° F. to about 150° F.

In some embodiments, provided herein is an edible metazoan biomass product (cultured edible product) comprising cells having any combination of the following cellular modifications: increased expression of GS, increased expression of IGF, increased expression of albumin, increased expression of telomerase reverse transcriptase (TERT), loss-of-function mutations in cyclin-dependent kinase inhibitor (CKI) proteins, increased expression of YAP, increased expression of TAZ, increased expression of myogenic transcription factors.

Cultivation Infrastructure

As referred to herein, a cultivation infrastructure refers to the environment in which metazoan cells are cultured, i.e. the environment in which the cellular biomass is cultivated.

A cultivation infrastructure may be a tube, a cylinder, a flask, a petri-dish, a multi-well plate, a dish, a vat, an incubator, a bioreactor, an industrial fermenter and the like. A cultivation infrastructure may be a culture medium in which metazoan cells are cultured.

A cultivation infrastructure can be of any scale, and support any volume of cellular biomass and culturing reagents. In some embodiments, the cultivation infrastructure ranges from about 10 μL to about 100,000 L. In exemplary embodiments, the cultivation infrastructure is about 10 μL, about 100 μL, about 1 mL, about 10 mL, about 100 mL, about 1 L, about 10 L, about 100 L, about 1000 L, about 10,000 L, or even about 100,000 L.

In some embodiments, the cultivation infrastructure comprises a substrate. A cultivation infrastructure may comprise a permeable substrate (e.g. permeable to physiological solutions) or an impermeable substrate (e.g. impermeable to physiological solutions).

In some embodiments, the cultivation infrastructure comprises a primary substrate, which can be a flat, concave, or convex substrate. In some embodiments, the cultivation infrastructure further comprises a secondary substrate, either introduced, or autologous, to direct cellular growth between the substrates, e.g. to direct attachment, proliferation and hypertrophy of cells on a plane perpendicular to the primary substrate.

In some embodiments, the cultivation infrastructure comprises a hydrogel, a liquid cell culture media, or soft agar.

In some embodiments, the cultivation infrastructure does not comprise a substrate to which cells can adhere. In some embodiments, the cultivation infrastructure comprises a suspension culture, e.g. supporting the growth of a self-adhering biomass, or single-cell suspension in a liquid medium.

In some embodiments, the cultivation infrastructure comprises adherent cells (i.e. those cells that adhere to a substrate). In some embodiments, the cultivation infrastructure comprises non-adherent cells (i.e. those cells that do not adhere to a substrate). In some embodiments, the cultivation infrastructure comprises both adherent and non-adherent cells.

Kits and Articles of Manufacture

The present application also provides kits for engineering cells of interest to increase production of glutamine, increase production of IGF, increase production of albumin, and/or decrease the production of ammonia.

In some embodiments, the kits comprise a GS DNA construct, an IGF construct, and/or an albumin construct for transfection. The kits optionally may further comprise tools for immortalization or extending cell self-renewal capacity, activating YAP/TAZ pathways, and myogenic differentiation.

The present application also provides articles of manufacture comprising any one of the compositions or kits described herein.

It is to be understood that the terminology employed herein is used for the purpose of describing particular embodiments only and is not intended to be limiting since the scope of the present invention will be limited only by the appended claims and equivalents thereof. The following examples are for illustrative purposes. These are intended to show certain aspects and embodiments of the present invention but are not intended to limit the invention in any manner.

EXAMPLES

Example 1: The Effects of Ectopic Expression of Glutamine Synthetase (GS) in Primary Duck Fibroblasts and Myoblasts

This example describes the effects of ectopic expression of GS on ammonia concentration in ambient media from primary duck fibroblast and myoblast cultures.

Methods

Measurement of Ammonia Concentration

Following the manufacturer's instructions (Sigma-Aldrich #AA0100), the absolute ammonia concentration (in μg/mL) was determined for each time point and treatment group (in biological triplicate). Results were reported as the mean of the treatment group bounded by the 95% confidence interval. Measurements of the ammonia detection assay were performed on a spectrophotometer (Spectramax 250). All statistical analyses and visualizations were performed in Microsoft Excel 2010.

Primary Duck Fibroblast and Myoblast Cultures

A peptide-coated (peptides mimicking extracellular matrix) T-150 flask was prepared for cell seeding by adding 10 mL of an aqueous peptide solution to the T-150 flask and incubated for at least 1 hour at 37° C. The aqueous peptide solution was aspirated from the T-150 flask and the flask washed with PBS. 25 mL of culture medium specific to the targeted cell type was added to the flask and the flask incubated and equilibrated at 37° C. in 5% atmospheric CO₂.

Under aseptic conditions the targeted tissue was excised with dissection instruments. Tissue sections were minced into approximately 2 mm×2 mm sections. 150 mg tissue sections were weighed and then transferred to a sterile 50 mL centrifuge tube containing 8 mL of enzymatic cell dissociation solution consisting of 0.17% trypsin and 0.085% collagenase in Hanks Balanced Salt Solution pH 7.4. The centrifuge tube was closed tightly and incubated on ice. Following overnight incubation, the tube was then incubated at 37° C. for 15 minutes. The enzymatic tissue digest was triturated with a sterile 5 mL serological pipet for 1 minute. The cell suspension was passed through a sterile 70 μm strainer into a sterile 50 mL centrifuge tube. 20 mL of cold basal medium was flowed through the strainer. The strainer was discarded and the tube capped. The centrifuge tube was centrifuged at 300×g for 5 minutes. The supernatant was aspirated, and the cell pellet was resuspended in culture medium before transfer to the T-150 flask prepared for seeding. The flask was incubated at 37° C. in 5% atmospheric CO₂. The cells were checked daily for growth and contamination. Culture medium was changed every two to three days. After the cultures reached a confluence of 70% to 90%, the cells were dissociated and either cryopreserved or passaged using standard cell culture technique.

Transfection

The primary duck fibroblast and myoblast cultures were routinely sub-cultured under 5% atmospheric CO₂ at 37° C. (i.e. incubation conditions) until 80% confluent on gelatin-coated dishes. Cells were dissociated to single cells and counted to determine the number of cells. In a gelatin-coated 12-well tissue culture plate, 5×10⁴ cells were seeded into each well. Growth culture medium was added to each well to a total final volume of 1 ml per well. The cells were incubated overnight at 37° C.

Cells were washed with PBS and transfection media added. 1 μg of plasmid DNA containing the murine GS coding sequence (pcDNA3.1+/C−(K)DYK (SEQ ID NO: 58), Genscript OMu19897D, Table 1A) driven by a CMV promoter was complexed using the Lipofectamine 3000 system (Thermo Fisher Scientific #L3000001). The complexed DNA was added dropwise to each well in biological triplicate. Vehicle control cells received an equivalent treatment absent the DNA. The cells were shaken gently and incubated for 48 hours; the media was then changed to proliferation media supplemented with 10% FBS and either the combination of 434 μg/mL (2 mM) L-alanyl-L-glutamine and 584 μg/mL (4 mM) L-glutamine or no supplemented glutamine (0 mM glutamine, “glutamine absent”). The cells were then returned to incubation conditions.

Conditioned Media Collection

Cells were washed with PBS, and 1 mL of either glutamine-supplemented or glutamine-absent proliferation medium was added to each well. Cells were then returned to incubation.

200 μL media samples were collected from each well and stored in sterile tubes at −80° C. In a gelatin-coated 12-well plate, proliferation medium was incubated in wells devoid of cells (i.e. acellular) in parallel experimental wells containing cells as a background control for ammonia accumulation.

Following each 24-hour period through day seven, 200 μL samples of media were collected from each well stored at −80° C. 200 μL of fresh medium were then added to each of the wells to a total volume of 1 mL. Following sample collection, the plates were then returned to incubation conditions.

Results

As demonstrated in FIG. 1, concentration of ammonia in media spontaneously increased in the absence of cells over the course of seven days. The rate at which ammonia increased differed between the three media conditions shown in the figure. Initial concentration of ammonia was largely dependent on whether or not the media had been supplemented with glutamine.

FIG. 2A-D shows that fibroblasts transfected with expression vectors coding for glutamine synthetase exhibited morphology similar to vehicle-only control transfected fibroblasts. Transfected fibroblasts remained viable and stable as evidenced by their continued adherence to substrate following a seven day incubation. FIG. 2A shows fibroblasts transfected with vehicle-only and grown in media with supplemented glutamine; FIG. 2B shows fibroblasts transfected with mouse GS and grown in media with supplemented glutamine; FIG. 2C shows fibroblasts transfected with vehicle-only and grown in media without supplemented glutamine; and FIG. 2D shows fibroblasts transfected with mouse GS and grown in media without supplemented glutamine.

As demonstrated in FIG. 3, following a one day incubation post transfection, fibroblasts expressing GS and grown in a culture medium supplemented with glutamine showed a smaller increase in extracellular ammonia than cells transfected with vehicle-only and grown in a culture medium supplemented with glutamine compared to a culture medium supplemented with glutamine in which no cells were grown. Within glutamine treatment groups, two-way ANOVA revealed a statistically significant difference (p<0.001) between ammonia concentration over time, dependent upon GS transfection and dependent on which day the measurement was made. The glutamine-supplemented culture medium in which no cells were grown showed an increase in ammonia concentration of 0.072 μg/mL/day, and the culture medium not supplemented with glutamine in which no cells were grown showed an increase in ammonia concentration of 0.51 μg/mL/day. It was observed on Day 3 that fibroblasts grown without supplemental ammonia and transfected with GS exhibited a statistically lower ammonia concentration compared to fibroblasts transfected with vehicle-only. Seven days following transfection, there was a significant difference (p<0.001, two-way ANOVA) in the amount of ammonia in glutamine absent growth media between cells transfected with GS and cells transfected with vehicle-only. Error bars in FIG. 3 indicate 95% confidence intervals. One asterisk indicates p<0.05; two asterisks indicate p<0.01.

FIG. 4 and Table 2 show normalized data from FIG. 3 to present a percent increase in ammonia relative to the extracellular ammonia concentration. After seven days in media without supplemented glutamine, fibroblasts transfected with GS showed a smaller increase in ammonia than cells transfected with vehicle-only.

TABLE 2
Percent Increase of Ammonia Relative to
Media-Only Ammonia Concentration

		+Glutamine	−Glutamine
		Media	Media
	Glutamine	43%	35%
	Synthetase
	Vehicle	43%	148%

As shown in FIG. 5, myoblasts transfected with expression vectors coding for GS exhibited morphology similar to vehicle treated myoblasts. Transfected cells remain viable and capable of normal differentiation as evidenced by spontaneous myotube formation. FIG. 5A shows myoblasts transfected with vehicle and grown in media with supplemented glutamine; FIG. 5B shows myoblasts transfected with a mouse GS gene and grown in a medium with supplemented glutamine; FIG. 5C shows myoblasts transfected with vehicle-only and grown in media without supplemented glutamine; and FIG. 5D shows myoblasts transfected with a mouse GS gene and grown in a medium without supplemented glutamine.

As demonstrated in FIG. 6, following a one-day incubation post transfection, myoblasts expressing GS and grown in media not supplemented with glutamine show less increase in ammonia in the media than myoblasts transfected with vehicle and grown in media not supplemented with glutamine compared to acellular control medium supplemented with glutamine. Additionally, following a one-day incubation post transfection, myoblasts expressing GS and grown in media supplemented with glutamine show less increase in ammonia in the media than myoblasts transfected with vehicle and grown in a medium supplemented with glutamine compared to a medium supplemented with glutamine in which no cells were grown. Glutamine-supplemented medium in which no cells were grown showed an increase in ammonia concentration of 0.34 μg/mL/day, and medium in which no cells were grown and not supplemented with glutamine increased by 0.51 μg/mL/day. It was observed on Day 3 that myoblasts grown without supplemental ammonia and transfected with GS exhibited a statistically lower ammonia concentration compared to fibroblasts transfected with vehicle. Seven days following transfection, there is a significant difference in the amount of ammonia in growth media between myoblasts transfected with GS and myoblasts transfected with vehicle. Two-way ANOVA revealed a statistically significant difference (p<0.001) between ammonia concentrations over time, dependent upon the presence or absence of glutamine, revealing that the effect of GS was statistically significant (p<0.001) only when glutamine was absent. Error bars in FIG. 6 indicate 95% confidence intervals. One asterisk indicates p<0.05; two asterisks indicate p<0.01. FIG. 7 and Table 3 normalize the data from FIG. 6 to show a percent increase in ammonia relative to the medium-only (medium without cells−control) concentration of ammonia. After seven days in media with or without supplemented glutamine, myoblasts transfected with GS show a smaller increase in ammonia than myoblasts transfected with vehicle.

TABLE 3
Percent Increase of Ammonia Relative to Media-
Only Ammonia Concentration

		+Glutamine	−Glutamine
		Media	Media
	Glutamine	40%	1%
	Synthetase
	Vehicle	67%	111%

FIG. 8 and Table 4 demonstrate that myoblast cultures show a reduction in ammonia in glutamine supplemented medium and an even larger percentage decrease in medium not supplemented with glutamine. Fibroblast cultures do not show a decrease in ammonia in glutamine supplemented media, but do exhibit a decrease in ammonia in media without supplemented glutamine.

TABLE 4
Percent Ammonia Remaining in
Media from +GS Cells Relative to
Media from −GS cells

		+Glutamine	−Glutamine
		Media	Media
	Myoblast	60%	1%
	Fibroblast	100%	24%

In both fibroblasts and myoblasts, transfection of GS resulted in statistically significant reduction of observed ammonia concentration compared to background ammonia generation (p<0.001, two-way ANOVA). In both cell types, there was a significant difference between ammonia concentrations in groups that were supplemented with glutamine compared to those that were not supplemented with glutamine (P<0.001). There was a statistically significant difference in cells transfected with GS compared to those transfected with vehicle alone when media was not supplemented with glutamine (p<0.001). The presence or absence of glutamine in cell culture media exhibits a significantly different effect between treatment groups (p<0.01, two-way ANOVA). Regression analysis reveals that the presence or absence of glutamine accounts for 72-98% of the variance of the data (p<0.001). Covariance analysis reveals strong positive interactions between systems where glutamine is present (4-12 fold greater than without glutamine), and a moderate interaction when cells are transfected with a GS gene or vehicle-only control, regardless of whether glutamine is present or not.

Based on data presented in FIG. 3, FIG. 9 illustrates cells transfected with a GS gene demonstrate a 6.8-fold delay in the time to achieve wild-type, primary cell ammonia concentration (in this instance, 14 μg/mL was observed on average and is indicated by horizontal dashed line). When controlled for the absence of supplemented glutamine, transfection of a GS gene accounts for 31% of this delay. Solid lines depict experimental data while dotted lines are extrapolated values based on a linear fit of the experimental data.

Example 2: The Effects of Ectopic Expression of IGF-1 and Albumin Expression in Primary Duck Fibroblasts and Myoblasts

This example describes the effects of ectopic expression of IGF-1 and albumin expression on the concentration of IGF-1 and albumin in media in primary duck fibroblasts and myoblasts.

Primary duck myoblast and fibroblast cells were isolated and cultured as described in Example 1. Cells were washed with PBS and transfection medium was added. 1 pg of plasmid DNA comprising a human serum albumin gene (Genscript OHu18744, Table 1A), a murine serum albumin gene (Genscript OMu21640, Table 1A) or human insulin-like growth factor 1 (IGF-1) (Origene RG212527, Table 1A) gene coding sequence fused to a nucleotide coding sequence encoding a FLAG-tag peptide (DYKDDDDK (SEQ ID NO: 57)) driven by a CMV promoter was complexed using the Lipofectamine 3000 system as a transfection vehicle (Thermo Fisher Scientific #L3000001). For transfection, the complexed DNA was added dropwise to each well in biological triplicate. Vehicle-only control cells received an equivalent treatment absent the DNA. The cell cultures were shaken gently and incubated for 48 hours; the transfection medium was then changed to growth medium and the cells were returned to incubation. Conditioned medium was collected as described in Example 1.

FIG. 10A-D show that fibroblasts transfected with a IGF-1 or albumin gene show morphology similar to cells transfected with vehicle-only (FIG. 10A Fibroblasts transfected with vehicle-only; FIG. 10B Fibroblasts transfected with a human IGF-1 gene; FIG. 10C Fibroblasts transfected with a mouse albumin gene; FIG. 10D Fibroblasts transfected with a human albumin gene).

FIG. 11A-D show that myoblasts transfected with an IGF-1 or albumin gene show morphology similar to cells transfected with vehicle-only (FIG. 11A Myoblasts transfected with vehicle-only; FIG. 11B Myoblasts transfected with a human IGF-1 gene; FIG. 11C Myoblasts transfected with a mouse albumin gene; FIG. 11D Myoblasts transfected with a human albumin gene).

Indirect ELISA detection assays were used to measure the secretion of IGF-1 into the ambient medium by the cells. Ambient culture media samples were thawed and maintained on ice until use. Total protein concentration in media samples was determined by absorbance measurement on a spectrophotometer (Spectramax 250) using a BCA serial dilution method (Thermo Fisher Scientific #22325). Using untreated black walled, black-bottomed polystyrene 96-well plates, 1 μg of total protein from each treatment was adsorbed to the plate using 1× coating buffer (Abcam #ab210899). Following coating, the wells were washed and blocked using a 5% solution of non-fat dry milk (NFDM) in 1×PBS. Primary antibody (murine anti-DDK monoclonal, Origene #OTI4C5) was incubated at 1:5000 dilution in 5% NFDM/PBS at 4° C. for 18 hours. Wells were washed with PBS for three cycles of shaking for five minutes per cycle. Secondary antibody (goat anti-mouse-HRP conjugate, Sigma AP130P) was applied at a 1:10000 dilution in 5% NFDM/PBS for 1.5 hours at 22° C. A second PBS wash/shake cycle was applied to remove excess secondary antibody. QuantaRed kit detection was applied as per manufacturer's instructions (Thermo Fisher Scientific #15159). Fluorescence emission values were obtained by a fluorometer (Tecan Infinite F200). Data was analyzed and visualized using Microsoft Excel 2010. Transfection with a plasmid encoding an IGF-1 protein resulted in a statistically significant 53% increase in secretion of IGF-1 into the ambient medium (FIG. 12) compared to vehicle-only transfected cells (p<0.001, one-way ANOVA) as measured by ELISA.

Example 3: Edible Metazoan Biomass Manufacturing Methods

The manufacturing of an edible metazoan biomass, in one exemplary protocol, can comprise three steps:

Step 1 is expanding cell populations overexpressing containing a GS gene, an IGF gene, an albumin gene, or a combination thereof in a cell line capable of self-renewal, wherein the cell line is a myogenic transcription factor-modified cell line, and wherein the cell line is of from a livestock, poultry, game or an aquatic animal species. Selected cell populations overexpressing targeted genes are seeded onto a substrate consisting of peptide-coated tissue-culture treated plastic, in a standard growth medium at a density of 7.5×10³ cells/cm² and cultured at 37° C. under 5% CO₂ atmospheric conditions. As cultures approach 80% confluence, cells are enzymatically dissociated and the expanded quantity of cells are seeded at 7.5×10³ cells/cm². This process is repeated until the total number of cells harvested following dissociation exceeds 1.0×10⁸ cells.

Step 2 is cryopreserving and storing the expanded cell populations in a cryopreserved cell bank. Cells harvested in quantities equal to or exceeding 1.0×10⁸ following expansion of selected cells are pelleted by centrifugation for 5 minutes at 300×g. The cell pellet is suspended in a standard cryopreservation medium at 2.5×10⁶ cells/mL and aliquoted at 1.0 mL per cryovial. Cryovials are cooled to −80° C. at −1° C./minute using an insulated container and transferred to a dewar containing liquid nitrogen for long-term storage. As cells stocks are depleted from this bank, remaining vials of cells are expanded and cryopreserved to replenish the cryopreserved cell bank inventory.

Step 3 is seeding and cultivating cells from a master cell bank in an ex vivo milieu: In accordance with the cultivation scale desired, one or more vials from the master cell bank is rapidly thawed to room temperature. The cryopreservation medium is removed from the cells by a 5 minute, 300×g centrifugation step. Cells are suspended in standard growth medium and seeded onto a gelatin-coated cultivation substrate in standard growth medium as before, except that, on the final passage prior to harvest, the cells are permitted to proliferate to 100% confluence on the cell culture substrate. The growth medium is next exchanged for differentiation medium specific to the myogenic transcription factor-modified cell line, and the cultures are permitted to differentiate for up to 6 days inducing myogenic differentiation of the cell line, wherein the differentiated cell line forms myocytes and multinucleated myotubes; and the myocytes and myotubes are cultured to generate skeletal muscle fibers.

The cultivation scale for proliferative biomass is outlined according to Table 5, where the predicted average cell mass is 2.0×10⁻⁹ grams, and the predicted average cell doubling time is 24 hours (h).

TABLE 5
Biomass Production Scale Cultivation Estimates During Cell Proliferation.
Masses are shown in grams. 1 vial is equivalent to 2.5 × 106 cells.

# hours	1 vial	2 vials	3 vials	4 vials	5 vials	6 vials	7 vials	8 vials	9 vials	10 vials

0 h	0.005	0.01	0.015	0.02	0.025	0.03	0.035	0.04	0.045	0.05
24 h	0.01	0.02	0.03	0.04	0.05	0.06	0.07	0.08	0.09	0.1
48 h	0.02	0.04	0.06	0.08	0.1	0.12	0.14	0.16	0.18	0.2
72 h	0.04	0.08	0.12	0.16	0.2	0.24	0.28	0.32	0.36	0.4
96 h	0.08	0.16	0.24	0.32	0.4	0.48	0.56	0.64	0.72	0.8
120 h	0.16	0.32	0.48	0.64	0.8	0.96	1.12	1.28	1.44	1.6
144 h	0.32	0.64	0.96	1.28	1.6	1.92	2.24	2.56	2.88	3.2
168 h	0.64	1.28	1.92	2.56	3.2	3.84	4.48	5.12	5.76	6.4
192 h	1.28	2.56	3.84	5.12	6.4	7.68	8.96	10.24	11.52	12.8
216 h	2.56	5.12	7.68	10.24	12.8	15.36	17.92	20.48	23.04	25.6
240 h	5.12	10.24	15.36	20.48	25.6	30.72	35.84	40.96	46.08	51.2
264 h	10.24	20.48	30.72	40.96	51.2	61.44	71.68	81.92	92.16	102.4
288 h	20.48	40.96	61.44	81.92	102.4	122.88	143.36	163.84	184.32	204.8
312 h	40.96	81.92	122.88	163.84	204.8	245.76	286.72	327.68	368.64	409.6
336 h	81.92	163.84	245.76	327.68	409.6	491.52	573.44	655.36	737.28	819.2

Step 4 is harvesting cultivated cell biomass for dietary consumption. After the cells have proliferated to confluence, the culture medium is removed, and the adherent cell cultures are rinsed with phosphate buffered saline. Next, the confluent biomass of adherent cells mechanically dissociated from the substrate by means of a scraping device. The dissociated biomass is collected into centrifuge tubes, pelleted at 400×g for 5 minutes to remove excess liquid, and processed for food product preparation. Harvested yield of differentiated cell biomass are estimated by multiplying the projected biomass of the proliferative culture by four to account for biomass accumulation during cell differentiation.

NUMBERED EMBODIMENTS

• 1. A method for increasing the cell density of a culture comprising metazoan cells, the method comprising:
  • a. introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), and albumin; and
  • b. culturing the cells in a cultivation infrastructure.
• 2. A method for increasing the cell density of a culture comprising metazoan cells, the method comprising:
  • a. introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof; and
  • b. culturing the cells in a cultivation infrastructure.
• 3. A method for increasing the cell density of a culture comprising metazoan cells, the method comprising:
  • a. introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof;
  • b. introducing into the cells a polynucleotide sequence encoding a telomerase reverse transcriptase (TERT); and
  • c. culturing the cells in a cultivation infrastructure.
• 4. The method of any one of embodiments 1-3, wherein the cells comprise a loss-of-function mutation in one or more genes encoding cyclin-dependent kinase inhibitor (CKI) proteins.
• 5. The method of embodiment 1 or 2, comprising introducing into the cells a polynucleotide sequence encoding a telomerase reverse transcriptase (TERT).
• 6. The method of embodiment 4, wherein the CKI proteins are p15, p16, paralogs, orthologs, or genetic variants thereof
• 7. The method of any one of embodiments 1-6, wherein the cells are from a self-renewing cell line.
• 8. The method of embodiment 7, wherein the self-renewing cell line is selected from the group consisting of an embryonic stem cell line, induced pluripotent stem cell line, extraembryonic cell line, and somatic cell line.
• 9. The method of any one of embodiments 1-8, wherein the cells are modified with a myogenic transcription factor.
• 10. The method of embodiment 9, wherein the myogenic transcription factor is MYOD1, MYOG, MYF5, MYF6, PAX3, PAX7, paralogs, orthologs, or genetic variants thereof
• 11. The method of any one of embodiments 1-10, wherein:
  • a. the concentration of glutamine in the culture medium is increased to at least 0.001 mM, to at least 0.0025 mM, to at least 0.005 mM, to at least 0.0075 mM, to at least 0.01 mM, to at least 0.025 mM, to at least 0.05 mM, to at least 0.075 mM, to at least 0.1 mM, to at least 0.25 mM, to at least 0.50 mM, to at least 0.75 mM, to at least 1.0 mM, to at least 1.5 mM, to at least 2.0 mM, to at least 3.0 mM, to at least 5.0 mM, to at least 10 mM, or to at least 20 mM;
  • b. the concentration of IGF in the culture medium is increased to at least 0.00001 ng/mL, to at least 0.000025 ng/mL, to at least 0.000075 ng/mL, to at least 0.0005 ng/mL, to at least 0.001 ng/mL, to at least 0.0025 ng/mL, to at least 0.005 ng/mL, to at least 0.0075 ng/mL, to at least 0.01 ng/mL, to at least 0.025 ng/mL, to at least 0.05 ng/mL, to at least 0.1 ng/mL, to at least 0.25 ng/mL, to at least 0.5 ng/mL, to at least 1 ng/mL, to at least 2.5 ng/mL, to at least 5 ng/mL, to at least 7.5 ng/mL, to at least 10 ng/mL, to at least 25 ng/mL, to at least 50 ng/mL, to at least 75 ng/mL, to at least 125 ng/mL, to at least 250 ng/mL, to at least 500 ng/mL, to at least 750 ng/mL, to at least 1,000 ng/mL, to at least 1,500 ng/mL, to at least 2,000 ng/mL, to at least 2,500 ng/mL, to at least 3,000 ng/mL, to at least 3,500 ng/mL, to at least 4,000 ng/mL, to at least 4,500 ng/mL, to at least 5,000 ng/mL to at least 6,000 ng/mL, to at least 7,000 ng/mL, to at least 8,000 ng/mL, to at least 9,000 ng/mL, or even by at least 10,000 ng/mL; and/or
  • c. the concentration of albumin in the culture medium is increased to at least 0.0001 mg/mL, to at least 0.0002 mg/mL, to at least 0.0004 mg/mL, to at least 0.0005 mg/mL, to at least 0.0006 mg/mL, to at least 0.0007 mg/mL, to at least 0.0008 mg/mL, to at least 0.0009 mg/mL, to at least 0.001 mg/mL, to at least 0.002 mg/mL, to at least 0.003 mg/mL, to at least 0.004 mg/mL, to at least 0.005 mg/mL, to at least 0.006 mg/mL, to at least 0.007 mg/mL, to at least 0.008 mg/mL, to at least 0.009 mg/mL, to at least 0.01 mg/mL, to at least 0.05 mg/mL, to at least 0.075 mg/mL, to at least 0.1 mg/mL, to at least 0.25 mg/mL, to at least 0.5 mg/mL, to at least 0.75 mg/mL, to at least 1 mg/mL, to at least mg/mL, to at least 1.5 mg/mL, to at least 1.5 mg/mL, to at least 1.75 mg/mL, to at least 2 mg/mL, to at least 3 mg/mL, to at least 5 mg/mL, to at least 10 mg/mL, to at least 20 mg/mL, to at least 25 mg/mL, to at least 50 mg/mL, to at least 75 mg/mL, or to at least 100 mg/mL,
  • compared to cultures of cells in which the expression of GS, IGF, albumin or a combination thereof is not increased.
• 12. The method of any one of embodiments 1-11, comprising inhibiting the HIPPO signaling pathway.
• 13. The method of embodiment 12, wherein inhibiting the HIPPO signaling pathway comprises activating Yes-Associated Protein 1 (YAP1), Transcriptional co-Activator with PDZ-binding motif (TAZ), or a combination thereof in the cells.
• 14. The method of any one of embodiments 1-13, wherein the cells are the cells of livestock, poultry, game or aquatic animal species.
• 15. The method of any one of embodiments 1-14, wherein the cells are of a chicken, duck, or turkey.
• 16. The method of any one of embodiments 1-14, wherein the cells are of a fish.
• 17. The method of any one of embodiments 1-14, wherein the cells are of a livestock species.
• 18. The method of embodiment 17, wherein the livestock species is porcine or bovine.
• 19. The method of any one of embodiments 1-14, wherein the cells are from any animal species intended for human or non-human dietary consumption.
• 20. The method of any one of embodiments 1-6, wherein the cells are myogenic cells.
• 21. The method of embodiment 20, wherein the myogenic cells are myoblasts, myocytes, satellite cells, side population cells, muscle derived stem cells, mesenchymal stem cells, myogenic pericytes, or mesoangioblasts.
• 22. The method of any one of embodiments 1-6, wherein the cells are non-myogenic cells.
• 23. The method of any one of embodiments 1-6, wherein the cells are non-myogenic cells modified to express one or more myogenic transcription factors.
• 24. The method of embodiment 23, wherein the myogenic transcription factor is MYOD1, MYOG, MYF5, MYF6, PAX3, PAX7, paralogs, orthologs, or genetic variants thereof
• 25. The method of any one of embodiments 1-24, wherein the polynucleotide sequence encoding GS comprises a GS gene sequence from Tables 1A and 1B.
• 26. The method of any one of embodiments 1-24, wherein the polynucleotide sequence encoding IGF comprises an IGF gene sequence from Tables 1A and 1B.
• 27. The method of any one of embodiments 1-24, wherein the polynucleotide sequence encoding albumin comprises an albumin gene sequence from Tables 1A and 1B.
• 28. An in vitro method for producing a cultured edible product, the method comprising:
  • a. introducing one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combinations thereof into myogenic cells;
  • b. optionally introducing a polynucleotide sequence encoding a telomerase reverse transcriptase (TERT) into the cells;
  • c. inducing myogenic differentiation of the cells expressing GS, IGF, albumin or combinations thereof and optionally TERT, wherein the differentiated cells form myocytes and multinucleated myotubes;
  • d. culturing the myocytes and myotubes to generate skeletal muscle fibers, thereby producing a cultured edible product.
• 29. The method of embodiment 28, wherein the myogenic cells are natively myogenic.
• 30. The method of embodiment 28, wherein the myogenic cells are not natively myogenic and are modified to express one or more myogenic transcription factors.
• 31. The method of embodiment 28 or 29, wherein the myogenic cells are myoblasts, myocytes, satellite cells, side population cells, muscle derived stem cells, mesenchymal stem cells, myogenic pericytes, or mesoangioblasts.
• 32. The method of embodiment 30, wherein the myogenic transcription factor is MYOD1, MYOG, MYF5, MYF6, PAX3, PAX7, paralogs, orthologs, or genetic variants thereof
• 33. The method of any one of embodiments 28-32, wherein the step of inducing myogenic differentiation comprises activating the expression of one or more myogenic transcription factors.
• 34. The method of any one of embodiments 28-33, comprising inhibiting the HIPPO signaling pathway.
• 35. The method of embodiment 34, wherein inhibiting the HIPPO signaling pathway comprises activating Yes-Associated Protein 1 (YAP1) and/or Transcriptional co-Activator with PDZ-binding motif (TAZ) in the cells.
• 36. The method of any one of embodiments 28-35, wherein the cells comprise a loss-of-function mutation in one or more genes encoding cyclin-dependent kinase inhibitor (CKI) proteins.
• 37. The method of embodiment 36, wherein the CKI proteins are p15, p16, paralogs, orthologs, or genetic variants thereof
• 38. The method of embodiment 30, wherein the myogenic cells are from an embryonic stem cell line, induced pluripotent stem cell line, extraembryonic cell line, or a somatic cell line, modified to express one or more myogenic transcription factors.
• 39. The method of any one of embodiments 28-38, wherein:
  • a. the concentration of glutamine in the culture medium is increased to at least 0.001 mM, to at least 0.0025 mM, to at least 0.005 mM, to at least 0.0075 mM, to at least 0.01 mM, to at least 0.025 mM, to at least 0.05 mM, to at least 0.075 mM, to at least 0.1 mM, to at least 0.25 mM, to at least 0.50 mM, to at least 0.75 mM, to at least 1.0 mM, to at least 1.5 mM, to at least 2.0 mM, to at least 3.0 mM, to at least 5.0 mM, to at least 10 mM, or to at least 20 mM;
  • b. the concentration of IGF in the culture medium is increased to at least 0.00001 ng/mL, to at least 0.000025 ng/mL, to at least 0.000075 ng/mL, to at least 0.0005 ng/mL, to at least 0.001 ng/mL, to at least 0.0025 ng/mL, to at least 0.005 ng/mL, to at least 0.0075 ng/mL, to at least 0.01 ng/mL, to at least 0.025 ng/mL, to at least 0.05 ng/mL, to at least 0.1 ng/mL, to at least 0.25 ng/mL, to at least 0.5 ng/mL, to at least 1 ng/mL, to at least 2.5 ng/mL, to at least 5 ng/mL, to at least 7.5 ng/mL, to at least 10 ng/mL, to at least 25 ng/mL, to at least 50 ng/mL, to at least 75 ng/mL, to at least 125 ng/mL, to at least 250 ng/mL, to at least 500 ng/mL, to at least 750 ng/mL, to at least 1,000 ng/mL, to at least 1,500 ng/mL, to at least 2,000 ng/mL, to at least 2,500 ng/mL, to at least 3,000 ng/mL, to at least 3,500 ng/mL, to at least 4,000 ng/mL, to at least 4,500 ng/mL, to at least 5,000 ng/mL to at least 6,000 ng/mL, to at least 7,000 ng/mL, to at least 8,000 ng/mL, to at least 9,000 ng/mL, or even by at least 10,000 ng/mL; and/or
  • c. the concentration of albumin in the culture medium is increased to at least 0.0001 mg/mL, to at least 0.0002 mg/mL, to at least 0.0004 mg/mL, to at least 0.0005 mg/mL, to at least 0.0006 mg/mL, to at least 0.0007 mg/mL, to at least 0.0008 mg/mL, to at least 0.0009 mg/mL, to at least 0.001 mg/mL, to at least 0.002 mg/mL, to at least 0.003 mg/mL, to at least 0.004 mg/mL, to at least 0.005 mg/mL, to at least 0.006 mg/mL, to at least 0.007 mg/mL, to at least 0.008 mg/mL, to at least 0.009 mg/mL, to at least 0.01 mg/mL, to at least 0.05 mg/mL, to at least 0.075 mg/mL, to at least 0.1 mg/mL, to at least 0.25 mg/mL, to at least 0.5 mg/mL, to at least 0.75 mg/mL, to at least 1 mg/mL, to at least mg/mL, to at least 1.5 mg/mL, to at least 1.5 mg/mL, to at least 1.75 mg/mL, to at least 2 mg/mL, to at least 3 mg/mL, to at least 5 mg/mL, to at least 10 mg/mL, to at least 20 mg/mL, to at least 25 mg/mL, to at least 50 mg/mL, to at least 75 mg/mL, or to at least 100 mg/mL,
  • compared to cultures of cells in which the expression of GS, IGF, albumin or a combination thereof is not increased.
• 40. The method of any one of embodiments 28-39, wherein the cells are from livestock, poultry, game or aquatic animal species.
• 41. The method of any one of embodiments 28-40, wherein the cells are from a chicken, duck, or turkey.
• 42. The method of any one of embodiments 28-40, wherein the cells are from a fish.
• 43. The method of any one of embodiments 28-40, wherein the cells are from a livestock species.
• 44. The method of embodiment 43, wherein the livestock species is porcine or bovine.
• 45. The method of any one of embodiments 28-44, wherein the cells are from any animal species intended for human or non-human dietary consumption.
• 46. The method of any one of embodiments 28-45, wherein the polynucleotide sequence encoding GS comprises a GS coding sequence from Tables 1A and 1B.
• 47. The method of any one of embodiments 28-45, wherein the polynucleotide sequence encoding IGF comprises an IGF coding sequence from Tables 1A and 1B.
• 48. The method of any one of embodiments 28-45, wherein the polynucleotide sequence encoding albumin comprises an albumin coding sequence from Tables 1A and 1B.
• 49. The method of any one of embodiments 1-48, wherein the cells express the GS protein at levels sufficient to decrease the ammonia production, increase the production of glutamine, or any combination thereof
• 50. A method of decreasing the concentration of ammonia and/or ammonium hydroxide in the medium of cells in culture comprising increasing the expression of a glutamine synthetase (GS) protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of ammonia (i.e. ammonium hydroxide) in the medium is decreased by at least 2.5%.
• 51. A method of increasing the production of glutamine in cells comprising increasing the expression of a glutamine synthetase (GS) protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of glutamine in the cells is increased by at least 2.5%.
• 52. The method of any one of embodiments 50-51, wherein the cells are modified to overexpress a gene encoding the GS protein.
• 53. The method of any one of embodiments 50-52, wherein the cells overexpress the gene encoding the GS protein at levels sufficient to decrease the ammonia production, increase the production of glutamine, or any combination thereof
• 54. A method of increasing the concentration of Insulin-like growth factor (IGF) in the medium of cells in culture comprising increasing the expression of an IGF protein in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of the IGF protein in the medium is increased by at least 2.5% or is increased to at least 0.001 ng/mL.
• 55. The method of embodiment 54, wherein the cells are modified to overexpress a gene encoding the IGF protein.
• 56. The method of any one of embodiments 54-55, wherein the cells overexpress the gene encoding the IGF protein at levels sufficient to increase the concentration of IGF in the medium.
• 57. The method of any one of embodiments 54-56, wherein the IGF protein is an IGF-1 protein.
• 58. The method of any one of embodiments 54-56, wherein the IGF protein is an IGF-2 protein.
• 59. A method of increasing the concentration of albumin in the medium of cells in culture comprising increasing the expression of albumin in the cells, wherein the cells are of livestock, poultry, game or aquatic animal species, and wherein the concentration of albumin in the medium is increased at least 2.5% or is increased to at least 0.1 μg/mL.
• 60. The method of embodiment 59, wherein the cells are modified to overexpress a gene encoding the albumin protein.
• 61. The method of any one of embodiments 59-60, wherein the cells overexpress the gene encoding the albumin protein at levels sufficient to increase the concentration of albumin in the medium.
• 62. The method of any one of embodiments 50-61, wherein the cells are a self-renewing cell line.
• 63. The method of embodiment 62, wherein the self-renewing cell line is selected from the group consisting of an embryonic stem cell line, induced pluripotent stem cell line, extraembryonic cell lines, and somatic cell lines.
• 64. The method of any one of embodiments 50-63, wherein the cell line is a myogenic transcription factor-modified cell line.
• 65. The method of embodiment 64, wherein the myogenic transcription factor is MYOD1, MYOG, MYF5, MYF6, PAX3, PAX7, paralogs, orthologs, or genetic variants thereof
• 66. The method of any one of embodiments 50-65, wherein the renewal capacity of the cells is extended.
• 67. The method of any one of embodiments 50-65, further comprising activating Telomerase reverse transcriptase (TERT) in the cells.
• 68. The method of any one of embodiments 50-67, wherein the cells comprise a loss-of-function mutation in one or more genes encoding cyclin-dependent kinase inhibitor (CKI) proteins.
• 69. The method of embodiment 68, wherein the CKI proteins are p15, p16, paralogs, orthologs, or genetic variants thereof
• 70. The method of any one of embodiments 50-67, comprising inhibiting the HIPPO signaling pathway in the cells.
• 71. The method of embodiment 70, wherein inhibiting the HIPPO signaling pathway comprises activating Yes-Associated Protein 1 (YAP1), Transcriptional co-Activator with PDZ-binding motif (TAZ), or a combination thereof in the cells.
• 72. The method of any one of embodiments 50-71, wherein the cell line is of a game species.
• 73. The method of any one of embodiments 50-71, wherein the cell line is of a poultry species.
• 74. The method of embodiment 73, wherein the poultry species is a duck.
• 75. The method of any one of embodiments 50-71, wherein the cell line is of an aquatic species.
• 76. The method of any one of embodiments 50-71, wherein the cell line is of a livestock species.
• 77. The method of embodiment 76, wherein the livestock species is porcine or bovine.
• 78. The method of any one of embodiments 50-71, wherein the cell line is from any animal species intended for human or non-human dietary consumption.
• 79. An in vitro method for producing a cultured edible product, the method comprising:
  • a. overexpressing a GS, IGF, albumin protein, or a combination thereof in a self-renewing cell line, wherein the cell line is a myogenic transcription factor-modified cell line, and wherein the cell line is of a livestock, poultry, game or aquatic animal species;
  • b. inducing myogenic differentiation of the cell line, wherein the differentiated cell line forms myocytes and multinucleated myotubes; and
  • c. culturing the myocytes and myotubes to generate skeletal muscle fibers, thereby producing a cultured edible product.
• 80. The method of embodiment 79, wherein the cell line is modified to overexpress a gene encoding the GS protein.
• 81. The method of embodiment 80, wherein the cell line is engineered to overexpress the gene encoding the GS protein at levels sufficient to decrease the ammonia production, increase the production of glutamine, or any combination thereof
• 82. The method of embodiment 79, wherein the cell line is modified to overexpress a gene encoding the IGF protein.
• 83. The method of embodiment 82, wherein the cells overexpress the gene encoding the IGF protein at levels sufficient to increase the production of IGF by the cells.
• 84. The method of any one of embodiments 79-83, wherein the IGF protein is an IGF-1 protein.
• 85. The method of any one of embodiments 79-83, wherein the IGF protein is an IGF-2 protein
• 86. The method of embodiment 79, wherein the cell line is modified to overexpress a gene encoding the albumin protein.
• 87. The method of embodiment 86, wherein the cells overexpress the gene encoding the albumin protein at levels sufficient to increase the concentration of albumin in cells.
• 88. The method of any one of embodiments 79-87, wherein the self-renewing cell line is selected from the group consisting of embryonic stem cells, induced pluripotent stem cells, extraembryonic cell lines, and somatic cell lines.
• 89. The method of any one of embodiments 79-88, wherein the myogenic transcription factor is the MYOD1, MYOG, MYF5, MYF6, PAX3, PAX7, paralogs, orthologs, or genetic variants thereof.
• 90. The method of any one of embodiments 79-89, wherein the renewal capacity of the cells is extended.
• 91. The method of any one of embodiments 79-89, further comprising activating Telomerase reverse transcriptase (TERT) in the cells.
• 92. The method of any one of embodiments 79-91, wherein the cells comprise a loss-of-function mutation in one or more genes encoding cyclin-dependent kinase inhibitor (CKI) proteins.
• 93. The method of embodiment 92, wherein the CKI proteins are p15, p16, paralogs, orthologs, or genetic variants thereof
• 94. The method of any one of embodiment 79-93, comprising inhibiting the HIPPO signaling pathway in the cells.
• 95. The method of embodiment 94, wherein the inhibition of the HIPPO signaling pathway comprises activating Yes-Associated Protein 1 (YAP1) and/or Transcriptional co-Activator with PDZ-binding motif (TAZ) in the cells.
• 96. The method of any one of embodiments 79-95, wherein the cell line is of a game species.
• 97. The method of any one of embodiments 79-95, wherein the cell line is of a poultry species.
• 98. The method of embodiment 97, wherein the poultry species is a duck.
• 99. The method of any one of embodiment 79-95, wherein the cell line is of an aquatic species.
• 100. The method of any one of embodiments 79-95, wherein the cell line is of a livestock species.
• 101. The method of embodiment 100, wherein the livestock species is porcine or bovine.
• 102. The method of any one of embodiments 79-95, wherein the cell line is from any animal species intended for human or non-human dietary consumption.
• 103. A cultured edible product produced by the in vitro method of any one of embodiments 28-49 and 79-102.
• 104. A cultured edible product comprising cells having increased expression of GS, increased expression of IGF, increased expression of albumin, and/or increased expression of TERT.
• 105. A construct comprising any one of the sequences selected from Table 1B.
• 106. An expression vector comprising any one of the sequences selected from Table 1B.
• 107. A cell comprising the expression vector of embodiment 106.
• 108. The cell of embodiment 107, wherein the cell is from a livestock, poultry, game, or aquatic species.
• 109. A method for increasing the secretion of glutamine by cells into a culture medium, the method comprising increasing the expression of a glutamine synthetase (GS) protein in the cells, wherein the cells are from livestock, poultry, game or aquatic animal species, and wherein the concentration of glutamine secreted into the culture medium is increased by at least 2.5%.
• 110. The method of embodiment 109, wherein the cells are modified to overexpress a gene encoding the GS protein.
• 111. The method of embodiment 109 or 110, comprising introducing into the cells a polynucleotide comprising a GS coding sequence from Table 1B.
• 112. The method of any one of embodiments 109-111, wherein the secretion of glutamine by cells into the culture medium is increased by at least 2.5% compared to cells in which the expression of GS is not increased.
• 113. A method for increasing the rate of proliferation of cells in a cultivation infrastructure, comprising:
  • a. introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof; and
  • b. culturing the cells in a cultivation infrastructure,
  • wherein the cells are from livestock, poultry, game or aquatic animal species.
• 114. The method of embodiment 113, wherein the polynucleotide sequence encoding GS comprises a GS coding sequence from Tables 1A and 1B.
• 115. The method of embodiment 113, wherein the polynucleotide sequence encoding IGF comprises an IGF coding sequence from Tables 1A and 1B.
• 116. The method of embodiment 113, wherein the polynucleotide sequence encoding albumin comprises an albumin coding sequence from Tables 1A and 1B.
• 117. The method of any one of embodiments 113-116, wherein the rate of proliferation of cells is increased by at least 5% compared to cells in which the expression of GS, IGF, albumin, or a combination thereof is not increased.
• 118. A method for decreasing death of cells in a cultivation infrastructure, comprising:
  • a. introducing into the cells one or more polynucleotide sequences encoding glutamine synthetase (GS), insulin-like growth factor (IGF), albumin or a combination thereof; and
  • b. culturing the cells in a cultivation infrastructure, wherein the cells are from livestock, poultry, game or aquatic animal species.
• 119. The method of embodiment 118, wherein the polynucleotide sequence encoding GS comprises a GS coding sequence from Tables 1A and 1B.
• 120. The method of embodiment 118, wherein the polynucleotide sequence encoding IGF comprises an IGF coding sequence from Tables 1A and 1B.
• 121. The method of embodiment 118, wherein the polynucleotide sequence encoding albumin comprises an albumin coding sequence from Tables 1A and 1B.
• 122. The method of any one of embodiment 118-121, wherein the cell death is decreased by at least 10% compared to cells in which the expression of GS, IGF, albumin, or a combination thereof is not increased.
• 123. A method for increasing protein production in cells in a cultivation infrastructure, comprising:
  • a. introducing into the cells a polynucleotide sequence encoding insulin-like growth factor (IGF); and
  • b. culturing the cells in a cultivation infrastructure, wherein the cells are from livestock, poultry, game or aquatic animal species.
• 124. The method of embodiment 123, wherein the polynucleotide sequence encoding IGF comprises an IGF coding sequence from Tables 1A and 1B.
• 125. The method of embodiment 123 or 124, wherein the IGF is IGF-1 or IGF-2.
• 126. The method of any one of embodiment 123-125, wherein the protein production measured as total cell protein per cell nucleus is increased by at least 5% compared to cells in which the expression of IGF is not increased.
• 127. The method of any one of embodiments 3, 28, 67, and 91, wherein the polynucleotide encoding TERT comprises a TERT coding sequence from Table 1B.