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Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing
Here, we efficiently generated transgenic cattle using two transposon systems (Sleeping Beauty and Piggybac) and their genomes were analyzed by next-generation sequencing (NGS). Blastocysts derived from microinjection of DNA transposons were selected and transferred into recipient cows. Nine transge...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914850/ https://www.ncbi.nlm.nih.gov/pubmed/27324781 http://dx.doi.org/10.1038/srep27185 |
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author | Yum, Soo-Young Lee, Song-Jeon Kim, Hyun-Min Choi, Woo-Jae Park, Ji-Hyun Lee, Won-Wu Kim, Hee-Soo Kim, Hyeong-Jong Bae, Seong-Hun Lee, Je-Hyeong Moon, Joo-Yeong Lee, Ji-Hyun Lee, Choong-Il Son, Bong-Jun Song, Sang-Hoon Ji, Su-Min Kim, Seong-Jin Jang, Goo |
author_facet | Yum, Soo-Young Lee, Song-Jeon Kim, Hyun-Min Choi, Woo-Jae Park, Ji-Hyun Lee, Won-Wu Kim, Hee-Soo Kim, Hyeong-Jong Bae, Seong-Hun Lee, Je-Hyeong Moon, Joo-Yeong Lee, Ji-Hyun Lee, Choong-Il Son, Bong-Jun Song, Sang-Hoon Ji, Su-Min Kim, Seong-Jin Jang, Goo |
author_sort | Yum, Soo-Young |
collection | PubMed |
description | Here, we efficiently generated transgenic cattle using two transposon systems (Sleeping Beauty and Piggybac) and their genomes were analyzed by next-generation sequencing (NGS). Blastocysts derived from microinjection of DNA transposons were selected and transferred into recipient cows. Nine transgenic cattle have been generated and grown-up to date without any health issues except two. Some of them expressed strong fluorescence and the transgene in the oocytes from a superovulating one were detected by PCR and sequencing. To investigate genomic variants by the transgene transposition, whole genomic DNA were analyzed by NGS. We found that preferred transposable integration (TA or TTAA) was identified in their genome. Even though multi-copies (i.e. fifteen) were confirmed, there was no significant difference in genome instabilities. In conclusion, we demonstrated that transgenic cattle using the DNA transposon system could be efficiently generated, and all those animals could be a valuable resource for agriculture and veterinary science. |
format | Online Article Text |
id | pubmed-4914850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49148502016-06-27 Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing Yum, Soo-Young Lee, Song-Jeon Kim, Hyun-Min Choi, Woo-Jae Park, Ji-Hyun Lee, Won-Wu Kim, Hee-Soo Kim, Hyeong-Jong Bae, Seong-Hun Lee, Je-Hyeong Moon, Joo-Yeong Lee, Ji-Hyun Lee, Choong-Il Son, Bong-Jun Song, Sang-Hoon Ji, Su-Min Kim, Seong-Jin Jang, Goo Sci Rep Article Here, we efficiently generated transgenic cattle using two transposon systems (Sleeping Beauty and Piggybac) and their genomes were analyzed by next-generation sequencing (NGS). Blastocysts derived from microinjection of DNA transposons were selected and transferred into recipient cows. Nine transgenic cattle have been generated and grown-up to date without any health issues except two. Some of them expressed strong fluorescence and the transgene in the oocytes from a superovulating one were detected by PCR and sequencing. To investigate genomic variants by the transgene transposition, whole genomic DNA were analyzed by NGS. We found that preferred transposable integration (TA or TTAA) was identified in their genome. Even though multi-copies (i.e. fifteen) were confirmed, there was no significant difference in genome instabilities. In conclusion, we demonstrated that transgenic cattle using the DNA transposon system could be efficiently generated, and all those animals could be a valuable resource for agriculture and veterinary science. Nature Publishing Group 2016-06-21 /pmc/articles/PMC4914850/ /pubmed/27324781 http://dx.doi.org/10.1038/srep27185 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yum, Soo-Young Lee, Song-Jeon Kim, Hyun-Min Choi, Woo-Jae Park, Ji-Hyun Lee, Won-Wu Kim, Hee-Soo Kim, Hyeong-Jong Bae, Seong-Hun Lee, Je-Hyeong Moon, Joo-Yeong Lee, Ji-Hyun Lee, Choong-Il Son, Bong-Jun Song, Sang-Hoon Ji, Su-Min Kim, Seong-Jin Jang, Goo Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing |
title | Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing |
title_full | Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing |
title_fullStr | Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing |
title_full_unstemmed | Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing |
title_short | Efficient generation of transgenic cattle using the DNA transposon and their analysis by next-generation sequencing |
title_sort | efficient generation of transgenic cattle using the dna transposon and their analysis by next-generation sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914850/ https://www.ncbi.nlm.nih.gov/pubmed/27324781 http://dx.doi.org/10.1038/srep27185 |
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