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http://dx.doi.org/10.5713/ajas.2009.80225

Production of Bovine Nuclear Transfer Embryos Using Fibroblasts Transfected with Single-Chain Human Follicle-Stimulating Hormone Gene  

Yoon, Ji Young (Department of Animal Sciences, Chungbuk National University)
Kwon, Mo Sun (Department of Physiology, Catholic University of Daegu School of Medicine)
Kang, Jee Hyun (Department of Physiology, Dankook University School of Medicine)
Ahn, Kwang Sung (Department of Physiology, Dankook University School of Medicine)
Kim, So Seob (Department of Biotechnology, Daegu University)
Kim, Nam-Hyung (Department of Animal Sciences, Chungbuk National University)
Kim, Jin-Hoi (Department of Animal Biotechnology, Konkuk University)
Kim, Teoan (Department of Physiology, Catholic University of Daegu School of Medicine)
Shim, Hosup (Department of Physiology, Dankook University School of Medicine)
Publication Information
Asian-Australasian Journal of Animal Sciences / v.22, no.2, 2009 , pp. 168-173 More about this Journal
Abstract
Human follicle-stimulating hormone (hFSH) is a pituitary glycoprotein that regulates follicular development and ovulation. Clinically, hFSH has been used to induce follicular growth in infertile women. The hormone is composed of heterodimers, including a common ${\alpha}$ subunit among the gonadotropin family and a hormone-specific ${\beta}$ subunit. Since assembly of the heterodimer is a rate-limiting step in the production of functional hFSH, transgenic clone cows carrying a single-chain hFSH transgene may efficiently produce functional hormone. Genes encoding the ${\alpha}$ and ${\beta}$ subunits of hFSH were linked using the C-terminal peptide sequence from the ${\beta}$ subunit of human chorionic gonadotropin. Bovine fetal fibroblasts were transfected with the gene construct, including the goat ${\beta}$-casein promoter and a single-chain hFSH coding sequence. Transfected fibroblasts were transferred into enucleated oocytes, and individual nuclear transfer (NT) embryos developed to the blastocyst stage were analyzed for the transgene by polymerase chain reaction. Seventy eight blastocysts (30.8%) were developed from 259 reconstructed embryos. Among these blastocysts, the hFSH gene was detected in 70.8% (34/48) of the embryos. Subsequent transfer of hFSH-transgenic clone embryos to 31 recipients results in 11 (35.5%) early pregnancies. However, all fetuses were lost before reaching day 180 of gestation. The results from this study demonstrated that bovine NT embryos carrying single-chain hFSH could be produced, and further extensive studies in which NT embryos are transferred to more recipients may give rise to single chain hFSH-transgenic cows for biomedical applications.
Keywords
Single-chain hFSH; Transgenic; Nuclear Transfer; Cow;
Citations & Related Records
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1 Baguisi, A., E. Behboodi, D. T. Melican, J. S. Pollock, M. M.Destrempes, C. Cammuso, J. L. Williams, S. D. Nims, C. A. Porter, P. Midura, M. J. Palacios, S. L. Ayres, R. S. Denniston, M. L. Hayes, C. A. Ziomek, H. M. Meade, R. A. Godke, W. G. Gavin, E. W. Overstrom and Y. Echelard. 1999. Production of goats by somatic cell nuclear transfer. Nat. Biotechnol. 17:456-461   DOI   ScienceOn
2 Farin, P. W., J. A. Piedrahita and C. E. Farin. 2006, Errors in development of fetuses and placentas from in vitro-produced bovine embryos, Theriogenol. 65:178-191   DOI   ScienceOn
3 Gordon, J. W., G. A. Scangos, D. J. Plotkin, J. A. Barbosa and F. H. Ruddle. 1980, Genetic transformation of mouse embryos by microinjection of purified DNA, Proc. Natl. Acad. Sci. USA.77:7380-7384   DOI   ScienceOn
4 Jahner, D., K. Hasse, R. Mulligan and R. Jaenisch. 1985. Insertion of the bacterial gpt gene into the germ line of mice by retroviral infection. Proc. Natl. Acad. Sci. USA. 82:6927-6931   DOI   ScienceOn
5 Lee, H. J., S. Hwang and J. T. Yoon. 2007, Effects of bovine somatotropin (bST) administration combined with controlled internal drug release (CIDR) on embryo quality and pregnancy of Hanwoo (Korean native beef cattle) during commercial embryo transfer program, Asian-Aust. J. Anim. Sci. 20:194-199
6 Pierce, J. G. and T. F. Parsons. 1981, Glycoprotein hormones: Structure and function, Annu. Rev. Biochem. 50:465-495   DOI   ScienceOn
7 Rosenkrans, C. F. J., G. Q. Zeng, G. T. McNamara, P. K. Schoff and N. L. First. 1993. Development of bovine embryos in vitro as affected by energy substrates. Biol. Reprod. 49:459-462   DOI   ScienceOn
8 Ruddon, R. W., S. A. Sherman and E. Bedows. 1996, Protein folding in the endoplasmic reticulum: lessons from the human chorionic gonadotropin beta subunit, Protein. Sci. 5:1443-1452   DOI   ScienceOn
9 Sugahara, T., A. Sato, M. Kudo, D. Ben-Menahem, M. R. Pixley, A. J. Hsueh and I. Boime. 1996, Expression of biologically active fusion genes encoding the common alpha subunit and the follicle-stimulating hormone beta subunit. Role of a linker sequence, J. Biol. Chem. 271:10445-10448   DOI   ScienceOn
10 Lavitrano, M., A. Camaioni, V. M. Fazio, S. Dolci, M. G. Farace and C. Spadafora. 1989, Sperm cells as vectors for introducing foreign DNA into eggs: Genetic transformation of mice, Cell57:717-723   DOI   ScienceOn
11 Fares, F. A., N. Suaanuma, K. Nishimori K, P. S. LaPolt. A. J. W. Hsueh and I. Boime. 1992, Design of a long-acting follitropin agonist by fusing the C-terminal sequence of the chorionic gonadotropin 8 subunit to follitropin 8 subunit, Proc. Natl. Acad. Sci. USA. 89:4304-4308   DOI   ScienceOn
12 Cibelli, J. B., R. P. Lanza, K. H. Campbell and M. D. West. 2002b, Principles of cloning. Academic Press, San Diego, California
13 Hwang, S., E. J. Choi, S. You, Y. J. Choi, K. S. Min and J. T. Yoon. 2006, Development of bovine nuclear transfer embryos using life-span extended donor cells transfected with foreign gene, Asian-Aust. J. Anim. Sci. 19:1574-1579
14 Lai, L., K. W. Park, H. T. Cheong, B. Kuhholzer, M. Samuel, A. Bonk, G. S. Im, A. Rieke, B. N. Day, C. N. Murphy, D. B. Carter and R. S. Prather. 2002. Transgenic pig expressing the enhanced green fluorescent protein produced by nuclear transfer using colchicine-treated fibroblasts as donor cells. Mol. Reprod. Dev. 62:300-306   DOI   ScienceOn
15 Kanegae, Y., G. Lee, Y. Sato, M. Tanaka, M. Nakai, T. Sakaki, S. Sugano and I. Saito. 1995, Efficient gene activation in mammalian cells by using recombinant adenovirus expressing site-specific Cre recombinase, Nucleic Acid Res,23:3816-3821   DOI   ScienceOn
16 Cibelli, J. B., K. H. Campbell, G. E. Seidel, M. D. West and R. P. Lanza. 2002a, The health profile of cloned animals, Nat. Biotechnol. 20:13-14   DOI   ScienceOn
17 Thotakura, N. R. and D. L. Blithe. 1995, Glycoprotein hormones: Glycobiology of gonadotrophins, thyrotrophin and free alpha subunit, Glycobiol. 5:3-10   DOI   ScienceOn
18 Cibelli, J. B., S. L. Stice, P. J. Golueke, J. J. Kane, J. Jerry, C.Blackwell, L. F. Ponce de Leon and J. M. Robl. 1998, Cloned transgenic calves produced from nonquiescent fetal fibroblasts, Sci. 280:1256-1258   DOI   PUBMED   ScienceOn
19 Schnieke, A. E., A. J. Kind, W. A. Ritchie, K. Mycock, A. R. Scott, M. Ritchie, I. Wilmut, A. Colman and K. H. Campbell, 1997,Human factor IX transgenic sheep produced by transfer of nuclei from transfected fetal fibroblasts, Sci. 278:2130-2133   DOI   PUBMED   ScienceOn
20 Young, L. E., K. D. Sinclair and I. Wilmut. 1998, Large offspring syndrome in cattle and sheep, Rev. Reprod. 3:155-163   DOI   ScienceOn