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 (pâ<â0.001) 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.
Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System.
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作者: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
| 期刊: | Scientific Reports | 影响因子: | 3.900 |
| 时间: | 2017 | 起止号: | 2017 Aug 4; 7(1):7301 |
| doi: | 10.1038/s41598-017-07223-7 | ||
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