Generation of Myostatin Gene-Edited Channel Catfish (Ictalurus punctatus) via Zygote Injection of CRISPR/Cas9 System

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作者
Karim Khalil
Medhat Elayat
Elsayed Khalifa
Samer Daghash
Ahmed Elaswad
Michael Miller
Hisham Abdelrahman
Zhi Ye
Ramjie Odin
David Drescher
Khoi Vo
Kamal Gosh
William Bugg
Dalton Robinson
Rex Dunham
机构
[1] Auburn University,School of Fisheries, Aquaculture and Aquatic Sciences
[2] Faculty of Veterinary Medicine,Anatomy and Embryology Department
[3] Cairo University,Harrison School of Pharmacy
[4] Auburn University,Department of Animal Wealth Development
[5] Faculty of Veterinary Medicine,Department of Veterinary Hygiene and Management
[6] Suez Canal University,undefined
[7] Faculty of Veterinary Medicine,undefined
[8] Cairo University,undefined
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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.
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