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Targeted mutagenesis in chicken using CRISPR/Cas9 system
The CRISPR/Cas9 system is a simple and powerful tool for genome editing in various organisms including livestock animals. However, the system has not been applied to poultry because of the difficulty in accessing their zygotes. Here we report the implementation of CRISPR/Cas9-mediated gene targeting...
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/PMC4822141/ https://www.ncbi.nlm.nih.gov/pubmed/27050479 http://dx.doi.org/10.1038/srep23980 |
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author | Oishi, Isao Yoshii, Kyoko Miyahara, Daichi Kagami, Hiroshi Tagami, Takahiro |
author_facet | Oishi, Isao Yoshii, Kyoko Miyahara, Daichi Kagami, Hiroshi Tagami, Takahiro |
author_sort | Oishi, Isao |
collection | PubMed |
description | The CRISPR/Cas9 system is a simple and powerful tool for genome editing in various organisms including livestock animals. However, the system has not been applied to poultry because of the difficulty in accessing their zygotes. Here we report the implementation of CRISPR/Cas9-mediated gene targeting in chickens. Two egg white genes, ovalbumin and ovomucoid, were efficiently (>90%) mutagenized in cultured chicken primordial germ cells (PGCs) by transfection of circular plasmids encoding Cas9, a single guide RNA, and a gene encoding drug resistance, followed by transient antibiotic selection. We transplanted CRISPR-induced mutant-ovomucoid PGCs into recipient chicken embryos and established three germline chimeric roosters (G0). All of the roosters had donor-derived mutant-ovomucoid spermatozoa, and the two with a high transmission rate of donor-derived gametes produced heterozygous mutant ovomucoid chickens as about half of their donor-derived offspring in the next generation (G1). Furthermore, we generated ovomucoid homozygous mutant offspring (G2) by crossing the G1 mutant chickens. Taken together, these results demonstrate that the CRISPR/Cas9 system is a simple and effective gene-targeting method in chickens. |
format | Online Article Text |
id | pubmed-4822141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48221412016-04-18 Targeted mutagenesis in chicken using CRISPR/Cas9 system Oishi, Isao Yoshii, Kyoko Miyahara, Daichi Kagami, Hiroshi Tagami, Takahiro Sci Rep Article The CRISPR/Cas9 system is a simple and powerful tool for genome editing in various organisms including livestock animals. However, the system has not been applied to poultry because of the difficulty in accessing their zygotes. Here we report the implementation of CRISPR/Cas9-mediated gene targeting in chickens. Two egg white genes, ovalbumin and ovomucoid, were efficiently (>90%) mutagenized in cultured chicken primordial germ cells (PGCs) by transfection of circular plasmids encoding Cas9, a single guide RNA, and a gene encoding drug resistance, followed by transient antibiotic selection. We transplanted CRISPR-induced mutant-ovomucoid PGCs into recipient chicken embryos and established three germline chimeric roosters (G0). All of the roosters had donor-derived mutant-ovomucoid spermatozoa, and the two with a high transmission rate of donor-derived gametes produced heterozygous mutant ovomucoid chickens as about half of their donor-derived offspring in the next generation (G1). Furthermore, we generated ovomucoid homozygous mutant offspring (G2) by crossing the G1 mutant chickens. Taken together, these results demonstrate that the CRISPR/Cas9 system is a simple and effective gene-targeting method in chickens. Nature Publishing Group 2016-04-06 /pmc/articles/PMC4822141/ /pubmed/27050479 http://dx.doi.org/10.1038/srep23980 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 Oishi, Isao Yoshii, Kyoko Miyahara, Daichi Kagami, Hiroshi Tagami, Takahiro Targeted mutagenesis in chicken using CRISPR/Cas9 system |
title | Targeted mutagenesis in chicken using CRISPR/Cas9 system |
title_full | Targeted mutagenesis in chicken using CRISPR/Cas9 system |
title_fullStr | Targeted mutagenesis in chicken using CRISPR/Cas9 system |
title_full_unstemmed | Targeted mutagenesis in chicken using CRISPR/Cas9 system |
title_short | Targeted mutagenesis in chicken using CRISPR/Cas9 system |
title_sort | targeted mutagenesis in chicken using crispr/cas9 system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822141/ https://www.ncbi.nlm.nih.gov/pubmed/27050479 http://dx.doi.org/10.1038/srep23980 |
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