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Journal of Veterinary Science ; : 405-407, 2011.
Artigo em Inglês | WPRIM | ID: wpr-186139

RESUMO

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.


Assuntos
Animais , Feminino , Masculino , Animais Geneticamente Modificados , Clonagem de Organismos/métodos , Cães/genética , Trato Gastrointestinal/metabolismo , Regulação da Expressão Gênica , Rim/metabolismo , Fígado/metabolismo , Proteínas Luminescentes/genética , Pulmão/metabolismo , Miocárdio/metabolismo , Técnicas de Transferência Nuclear/veterinária , Baço/metabolismo , Traqueia/metabolismo
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