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Letters to Nature
Nature 380, 64 - 66 (07 March 1996); doi:10.1038/380064a0

Sheep cloned by nuclear transfer from a cultured cell line

K. H. S. Campbell, J. McWhir, W. A. Ritchie & I. Wilmut

Roslin Institute (Edinburgh), Roslin, Midlothian EH25 9PS, UK

NUCLEAR transfer has been used in mammals as both a valuable tool in embryological studies1 and as a method for the multiplication of 'elite' embryos2–4. Offspring have only been reported when early embryos, or embryo-derived cells during primary culture, were used as nuclear donors5,6. Here we provide the first report, to our knowledge, of live mammalian offspring following nuclear transfer from an established cell line. Lambs were born after cells derived from sheep embryos, which had been cultured for 6 to 13 passages, were induced to quiesce by serum starvation before transfer of their nuclei into enucleated oocytes. Induction of quiescence in the donor cells may modify the donor chromatin structure to help nuclear reprogramming and allow development. This approach will provide the same powerful opportunities for analysis and modification of gene function in livestock species that are available in the mouse through the use of embryonic stem cells7.

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References
1. McGrath, J. & Solter, D. Science 220, 1300−1302 (1983). | PubMed | ISI | ChemPort |
2. Bondioli, K. R., Westhusin, M. E. & Looney, C. R. Therio 33, 165−174 (1990).
3. Prather, R. S. & First, N. L. Int. Rev. Cytol. 120, 169−190 (1990). | PubMed | ChemPort |
4. Chesne, P., Heyman, Y., Peynot, N. & Renard, J.-P. C.r. Acad. Sci. Paris Life Sci. 316, 487−491 (1993). | ChemPort |
5. Sims, M. & First, N. L. Proc. natn. Acad. Sci. U.S.A. 91, 6243−6147 (1994).
6. Collas, P. & Barnes, F. L. Molec. Repr. Dev. 38, 264−267 (1994). | ChemPort |
7. Hooper, M. L. Embryonal Stem Cells: Introducing Planned Changes into the Germline (ed. Evans, H. J.) (Harwood Academic, Switzerland, 1992).
8. Galli, C., Lazzari, G., Flechon, J. & Moor, R. M. Zygote 2, 385−389 (1994). | PubMed | ChemPort |
9. Campbell, K. H. S., Ritchie, W. A. & Wilmut, I. Biol. Reprod. 49, 933−942 (1993). | PubMed | ISI | ChemPort |
10. Campbell, K. H. S., Loi, P., Capai, P. & Wilmut, I. Biol. Reprod. 50, 1385−1393 (1994). | PubMed | ChemPort |
11. Szollosi, D., Czolowska, R., Szollosi, M. S. & Tarkowski, A. K. J. Cell Sci. 91, 603−613 (1988). | PubMed |
12. Whitten, W. K. & Biggers, J. D. J. Reprod. Fertil. 17, 399−401 (1968). | PubMed | ChemPort |
13. Breslaw, N. E. & Clayton, D. G. J. Am. Stat. Assoc. 88, 9−25 (1993).
14. Whitfield, J. F., Boynton, A. L., Rixon, R. H. & Youdale, T. Control of Animal Cell Proliferation Vol. 1 (eds Boynton, A. L. & Leffert, H. L.) 331−365 (Academic, London 1985).
15. Piedrahita, J. A., Anderson, G. B. & Bon Durrant, R. H. Therio 34, 879−901 (1990).
16. Gerfen, R. W. & Wheeler, M. B. Anim. Biotechnol. 6, 1−14 (1995).
17. Willadsen, S. M. Nature 320, 63−65 (1986). | Article | PubMed | ISI | ChemPort |
18. Buchanan, F. C., Galloway, S. M. & Crawford, A. M. Anim. Genet. 25, 60 (1994). | PubMed | ChemPort |



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