Post-mortem re-cloning of a transgenic red fluorescent protein dog

Recently, the world's first transgenic dogs were produced by somatic cell nuclear transfer. However, cellular senescence is a major limiting factor for producing more advanced transgenic dogs. To overcome this obstacle, we rejuvenated transgenic cells using a re-cloning technique. Fibroblasts f...

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Veröffentlicht in:Journal of veterinary science (Suwŏn-si, Korea) 2011, 12(4), , pp.405-407
Hauptverfasser: Hong, S.G., Seoul National University, Seoul, Republic of Korea, Koo, O.J., Seoul National University, Seoul, Republic of Korea, Oh, H.J., Seoul National University, Seoul, Republic of Korea, Park, J.E., Seoul National University, Seoul, Republic of Korea, Kim, M.J., Seoul National University, Seoul, Republic of Korea, Kim, G.A., Seoul National University, Seoul, Republic of Korea, Park, E.J., Seoul National University, Seoul, Republic of Korea, Jang, G., Seoul National University, Seoul, Republic of Korea, Lee, B.C., Seoul National University, Seoul, Republic of Korea
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Sprache:eng
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Zusammenfassung:Recently, the world's first transgenic dogs were produced by somatic cell nuclear transfer. However, cellular senescence is a major limiting factor for producing more advanced transgenic dogs. To overcome this obstacle, we rejuvenated transgenic cells using a re-cloning technique. Fibroblasts from post-mortem red fluorescent protein (RFP) dog were reconstructed with in vivo matured oocytes and transferred into 10 surrogate dogs. One puppy was produced and confirmed as a re-cloned dog. Although the puppy was lost during birth, we successfully established a rejuvenated fibroblast cell line from this animal. The cell line was found to stably express RFP and is ready for additional genetic modification.
ISSN:1229-845X
1976-555X
DOI:10.4142/jvs.2011.12.4.405