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Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System
The myostatin (MSTN) gene is important because of its role in regulation of skeletal muscle growth in all vertebrates. In this study, CRISPR/Cas9 was utilized to successfully target the channel catfish, Ictalurus punctatus, muscle suppressor gene MSTN. CRISPR/Cas9 induced high rates (88–100%) of mut...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544710/ https://www.ncbi.nlm.nih.gov/pubmed/28779173 http://dx.doi.org/10.1038/s41598-017-07223-7 |
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author | Khalil, Karim Elayat, Medhat Khalifa, Elsayed Daghash, Samer Elaswad, Ahmed Miller, Michael Abdelrahman, Hisham Ye, Zhi Odin, Ramjie Drescher, David Vo, Khoi Gosh, Kamal Bugg, William Robinson, Dalton Dunham, Rex |
author_facet | Khalil, Karim Elayat, Medhat Khalifa, Elsayed Daghash, Samer Elaswad, Ahmed Miller, Michael Abdelrahman, Hisham Ye, Zhi Odin, Ramjie Drescher, David Vo, Khoi Gosh, Kamal Bugg, William Robinson, Dalton Dunham, Rex |
author_sort | Khalil, Karim |
collection | PubMed |
description | The myostatin (MSTN) gene is important because of its role in regulation of skeletal muscle growth in all vertebrates. In this study, CRISPR/Cas9 was utilized to successfully target the channel catfish, Ictalurus punctatus, muscle suppressor gene MSTN. CRISPR/Cas9 induced high rates (88–100%) of mutagenesis in the target protein-encoding sites of MSTN. MSTN-edited fry had more muscle cells (p < 0.001) than controls, and the mean body weight of gene-edited fry increased by 29.7%. The nucleic acid alignment of the mutated sequences against the wild-type sequence revealed multiple insertions and deletions. These results demonstrate that CRISPR/Cas9 is a highly efficient tool for editing the channel catfish genome, and opens ways for facilitating channel catfish genetic enhancement and functional genomics. This approach may produce growth-enhanced channel catfish and increase productivity. |
format | Online Article Text |
id | pubmed-5544710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55447102017-08-07 Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System Khalil, Karim Elayat, Medhat Khalifa, Elsayed Daghash, Samer Elaswad, Ahmed Miller, Michael Abdelrahman, Hisham Ye, Zhi Odin, Ramjie Drescher, David Vo, Khoi Gosh, Kamal Bugg, William Robinson, Dalton Dunham, Rex Sci Rep Article The myostatin (MSTN) gene is important because of its role in regulation of skeletal muscle growth in all vertebrates. In this study, CRISPR/Cas9 was utilized to successfully target the channel catfish, Ictalurus punctatus, muscle suppressor gene MSTN. CRISPR/Cas9 induced high rates (88–100%) of mutagenesis in the target protein-encoding sites of MSTN. MSTN-edited fry had more muscle cells (p < 0.001) than controls, and the mean body weight of gene-edited fry increased by 29.7%. The nucleic acid alignment of the mutated sequences against the wild-type sequence revealed multiple insertions and deletions. These results demonstrate that CRISPR/Cas9 is a highly efficient tool for editing the channel catfish genome, and opens ways for facilitating channel catfish genetic enhancement and functional genomics. This approach may produce growth-enhanced channel catfish and increase productivity. Nature Publishing Group UK 2017-08-04 /pmc/articles/PMC5544710/ /pubmed/28779173 http://dx.doi.org/10.1038/s41598-017-07223-7 Text en © The Author(s) 2017 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 Khalil, Karim Elayat, Medhat Khalifa, Elsayed Daghash, Samer Elaswad, Ahmed Miller, Michael Abdelrahman, Hisham Ye, Zhi Odin, Ramjie Drescher, David Vo, Khoi Gosh, Kamal Bugg, William Robinson, Dalton Dunham, Rex Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System |
title | Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System |
title_full | Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System |
title_fullStr | Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System |
title_full_unstemmed | Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System |
title_short | Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System |
title_sort | generation of myostatin gene-edited channel catfish (ictalurus punctatus) via zygote injection of crispr/cas9 system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544710/ https://www.ncbi.nlm.nih.gov/pubmed/28779173 http://dx.doi.org/10.1038/s41598-017-07223-7 |
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