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Successful cloning of a superior buffalo bull

Somatic cell nuclear transfer (SCNT) technology provides an opportunity to multiply superior animals that could speed up dissemination of favorable genes into the population. In the present study, we attempted to reproduce a superior breeding bull of Murrah buffalo, the best dairy breed of buffalo,...

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Autores principales: Selokar, Naresh L., Sharma, Papori, Saini, Monika, Sheoran, Suman, Rajendran, Rasika, Kumar, Dharmendra, Sharma, Rakesh Kumar, Motiani, Rajender K., Kumar, Pradeep, Jerome, A, Khanna, Sudhir, Yadav, Prem Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684639/
https://www.ncbi.nlm.nih.gov/pubmed/31388074
http://dx.doi.org/10.1038/s41598-019-47909-8
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author Selokar, Naresh L.
Sharma, Papori
Saini, Monika
Sheoran, Suman
Rajendran, Rasika
Kumar, Dharmendra
Sharma, Rakesh Kumar
Motiani, Rajender K.
Kumar, Pradeep
Jerome, A
Khanna, Sudhir
Yadav, Prem Singh
author_facet Selokar, Naresh L.
Sharma, Papori
Saini, Monika
Sheoran, Suman
Rajendran, Rasika
Kumar, Dharmendra
Sharma, Rakesh Kumar
Motiani, Rajender K.
Kumar, Pradeep
Jerome, A
Khanna, Sudhir
Yadav, Prem Singh
author_sort Selokar, Naresh L.
collection PubMed
description Somatic cell nuclear transfer (SCNT) technology provides an opportunity to multiply superior animals that could speed up dissemination of favorable genes into the population. In the present study, we attempted to reproduce a superior breeding bull of Murrah buffalo, the best dairy breed of buffalo, using donor cells that were established from tail-skin biopsy and seminal plasma. We studied several parameters such as cell cycle stages, histone modifications (H3K9ac and H3K27me3) and expression of developmental genes in donor cells to determine their SCNT reprogramming potentials. We successfully produced the cloned bull from an embryo that was produced from the skin-derived cell. Growth, blood hematology, plasma biochemistries, and reproductive organs of the produced cloned bull were found normal. Subsequently, the bull was employed for semen production. Semen parameters such as CASA (Computer Assisted Semen Analysis) variables and in vitro fertilizing ability of sperms of the cloned bull were found similar to non-cloned bulls, including the donor bull. At present, we have 12 live healthy progenies that were produced using artificial insemination of frozen semen of the cloned bull, which indicate that the cloned bull is fertile and can be utilized in the buffalo breeding schemes. Taken together, we demonstrate that SCNT can be used to reproduce superior buffalo bulls.
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spelling pubmed-66846392019-08-11 Successful cloning of a superior buffalo bull Selokar, Naresh L. Sharma, Papori Saini, Monika Sheoran, Suman Rajendran, Rasika Kumar, Dharmendra Sharma, Rakesh Kumar Motiani, Rajender K. Kumar, Pradeep Jerome, A Khanna, Sudhir Yadav, Prem Singh Sci Rep Article Somatic cell nuclear transfer (SCNT) technology provides an opportunity to multiply superior animals that could speed up dissemination of favorable genes into the population. In the present study, we attempted to reproduce a superior breeding bull of Murrah buffalo, the best dairy breed of buffalo, using donor cells that were established from tail-skin biopsy and seminal plasma. We studied several parameters such as cell cycle stages, histone modifications (H3K9ac and H3K27me3) and expression of developmental genes in donor cells to determine their SCNT reprogramming potentials. We successfully produced the cloned bull from an embryo that was produced from the skin-derived cell. Growth, blood hematology, plasma biochemistries, and reproductive organs of the produced cloned bull were found normal. Subsequently, the bull was employed for semen production. Semen parameters such as CASA (Computer Assisted Semen Analysis) variables and in vitro fertilizing ability of sperms of the cloned bull were found similar to non-cloned bulls, including the donor bull. At present, we have 12 live healthy progenies that were produced using artificial insemination of frozen semen of the cloned bull, which indicate that the cloned bull is fertile and can be utilized in the buffalo breeding schemes. Taken together, we demonstrate that SCNT can be used to reproduce superior buffalo bulls. Nature Publishing Group UK 2019-08-06 /pmc/articles/PMC6684639/ /pubmed/31388074 http://dx.doi.org/10.1038/s41598-019-47909-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Selokar, Naresh L.
Sharma, Papori
Saini, Monika
Sheoran, Suman
Rajendran, Rasika
Kumar, Dharmendra
Sharma, Rakesh Kumar
Motiani, Rajender K.
Kumar, Pradeep
Jerome, A
Khanna, Sudhir
Yadav, Prem Singh
Successful cloning of a superior buffalo bull
title Successful cloning of a superior buffalo bull
title_full Successful cloning of a superior buffalo bull
title_fullStr Successful cloning of a superior buffalo bull
title_full_unstemmed Successful cloning of a superior buffalo bull
title_short Successful cloning of a superior buffalo bull
title_sort successful cloning of a superior buffalo bull
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684639/
https://www.ncbi.nlm.nih.gov/pubmed/31388074
http://dx.doi.org/10.1038/s41598-019-47909-8
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