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Production of second-generation cloned cats by somatic cell nuclear transfer
We successfully produced second-generation cloned cats by somatic cell nuclear transfer (SCNT) using skin cells from a cloned cat. Skin cells from an odd-eyed, all-white male cat (G0 donor cat) were used to generate a cloned cat (G1 cloned cat). At 6 months of age, skin cells from the G1 cloned cat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127140/ https://www.ncbi.nlm.nih.gov/pubmed/18358524 http://dx.doi.org/10.1016/j.theriogenology.2008.01.017 |
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author | Yin, X.J. Lee, H.S. Yu, X.F. Kim, L.H. Shin, H.D. Cho, S.J. Choi, E.G. Kong, I.K. |
author_facet | Yin, X.J. Lee, H.S. Yu, X.F. Kim, L.H. Shin, H.D. Cho, S.J. Choi, E.G. Kong, I.K. |
author_sort | Yin, X.J. |
collection | PubMed |
description | We successfully produced second-generation cloned cats by somatic cell nuclear transfer (SCNT) using skin cells from a cloned cat. Skin cells from an odd-eyed, all-white male cat (G0 donor cat) were used to generate a cloned cat (G1 cloned cat). At 6 months of age, skin cells from the G1 cloned cat were used for SCNT to produce second-generation cloned cats. We compared the in vitro and in vivo development of SCNT embryos that were derived from the G0 donor and G1 cloned donor cat's skin fibroblasts. The nuclei from the G0 donor and G1 cloned donor cat's skin fibroblasts fused with enucleated oocytes with equal rates of fusion (60.7% vs. 58.8%, respectively) and cleavage (66.3% vs. 63.4%). The 2–4-cell SCNT embryos were then transferred into recipients. One of the five recipients of G0 donor derived NT embryos (20%) delivered one live male cloned kitten, whereas 4 of 15 recipients of the G1 cloned donor cat derived NT embryos (26%) delivered a total of seven male second-generation cloned kittens (four live kittens from one surrogate, plus two stillborn kittens, and one live kitten that died 2 d after birth from three other surrogate mothers). The four second-generation cloned kittens from the same surrogate all had a white coat color; three of the four second-generation cloned kittens had two blue eyes, and one of the second-generation cloned kittens had an odd-eye color. Despite low cloning efficiency, cloned cats can be used as donor cats to produce second-generation cloned cats. |
format | Online Article Text |
id | pubmed-7127140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71271402020-04-06 Production of second-generation cloned cats by somatic cell nuclear transfer Yin, X.J. Lee, H.S. Yu, X.F. Kim, L.H. Shin, H.D. Cho, S.J. Choi, E.G. Kong, I.K. Theriogenology Article We successfully produced second-generation cloned cats by somatic cell nuclear transfer (SCNT) using skin cells from a cloned cat. Skin cells from an odd-eyed, all-white male cat (G0 donor cat) were used to generate a cloned cat (G1 cloned cat). At 6 months of age, skin cells from the G1 cloned cat were used for SCNT to produce second-generation cloned cats. We compared the in vitro and in vivo development of SCNT embryos that were derived from the G0 donor and G1 cloned donor cat's skin fibroblasts. The nuclei from the G0 donor and G1 cloned donor cat's skin fibroblasts fused with enucleated oocytes with equal rates of fusion (60.7% vs. 58.8%, respectively) and cleavage (66.3% vs. 63.4%). The 2–4-cell SCNT embryos were then transferred into recipients. One of the five recipients of G0 donor derived NT embryos (20%) delivered one live male cloned kitten, whereas 4 of 15 recipients of the G1 cloned donor cat derived NT embryos (26%) delivered a total of seven male second-generation cloned kittens (four live kittens from one surrogate, plus two stillborn kittens, and one live kitten that died 2 d after birth from three other surrogate mothers). The four second-generation cloned kittens from the same surrogate all had a white coat color; three of the four second-generation cloned kittens had two blue eyes, and one of the second-generation cloned kittens had an odd-eye color. Despite low cloning efficiency, cloned cats can be used as donor cats to produce second-generation cloned cats. Elsevier Inc. 2008-05 2008-03-20 /pmc/articles/PMC7127140/ /pubmed/18358524 http://dx.doi.org/10.1016/j.theriogenology.2008.01.017 Text en Copyright © 2008 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Yin, X.J. Lee, H.S. Yu, X.F. Kim, L.H. Shin, H.D. Cho, S.J. Choi, E.G. Kong, I.K. Production of second-generation cloned cats by somatic cell nuclear transfer |
title | Production of second-generation cloned cats by somatic cell nuclear transfer |
title_full | Production of second-generation cloned cats by somatic cell nuclear transfer |
title_fullStr | Production of second-generation cloned cats by somatic cell nuclear transfer |
title_full_unstemmed | Production of second-generation cloned cats by somatic cell nuclear transfer |
title_short | Production of second-generation cloned cats by somatic cell nuclear transfer |
title_sort | production of second-generation cloned cats by somatic cell nuclear transfer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127140/ https://www.ncbi.nlm.nih.gov/pubmed/18358524 http://dx.doi.org/10.1016/j.theriogenology.2008.01.017 |
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