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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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Autores principales: Hong, So Gun, Koo, Ok Jae, Oh, Hyun Ju, Park, Jung Eun, Kim, Minjung, Kim, Geon-A, Park, Eun Jung, Jang, Goo, Lee, Byeong-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232402/
https://www.ncbi.nlm.nih.gov/pubmed/22122908
http://dx.doi.org/10.4142/jvs.2011.12.4.405
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author Hong, So Gun
Koo, Ok Jae
Oh, Hyun Ju
Park, Jung Eun
Kim, Minjung
Kim, Geon-A
Park, Eun Jung
Jang, Goo
Lee, Byeong-Chun
author_facet Hong, So Gun
Koo, Ok Jae
Oh, Hyun Ju
Park, Jung Eun
Kim, Minjung
Kim, Geon-A
Park, Eun Jung
Jang, Goo
Lee, Byeong-Chun
author_sort Hong, So Gun
collection PubMed
description 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.
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spelling pubmed-32324022011-12-08 Post-mortem re-cloning of a transgenic red fluorescent protein dog Hong, So Gun Koo, Ok Jae Oh, Hyun Ju Park, Jung Eun Kim, Minjung Kim, Geon-A Park, Eun Jung Jang, Goo Lee, Byeong-Chun J Vet Sci Short Communication 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. The Korean Society of Veterinary Science 2011-12 2011-11-30 /pmc/articles/PMC3232402/ /pubmed/22122908 http://dx.doi.org/10.4142/jvs.2011.12.4.405 Text en Copyright © 2011 The Korean Society of Veterinary Science https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Hong, So Gun
Koo, Ok Jae
Oh, Hyun Ju
Park, Jung Eun
Kim, Minjung
Kim, Geon-A
Park, Eun Jung
Jang, Goo
Lee, Byeong-Chun
Post-mortem re-cloning of a transgenic red fluorescent protein dog
title Post-mortem re-cloning of a transgenic red fluorescent protein dog
title_full Post-mortem re-cloning of a transgenic red fluorescent protein dog
title_fullStr Post-mortem re-cloning of a transgenic red fluorescent protein dog
title_full_unstemmed Post-mortem re-cloning of a transgenic red fluorescent protein dog
title_short Post-mortem re-cloning of a transgenic red fluorescent protein dog
title_sort post-mortem re-cloning of a transgenic red fluorescent protein dog
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232402/
https://www.ncbi.nlm.nih.gov/pubmed/22122908
http://dx.doi.org/10.4142/jvs.2011.12.4.405
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