No abstract

No abstract

Many studies have been conducted to improve economically important livestock traits such as feed efficiency and muscle growth. Genome editing technologies represent a major advancement for both basic research and agronomic biotechnology development. The clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technical platform is a powerful tool used to engineer specific targeted loci. However, the potential occurrence of off‐target effects, including the cleavage of unintended targets, limits the practical applications of Cas9‐mediated genome editing. In this study, to minimize the off‐target effects of this technology, we utilized D10A‐Cas9 nickase to generate myostatin‐knockout (MSTN KO) chickens via primordial germ cells. D10A‐Cas9 nickase (Cas9n)‐mediated MSTN KO chickens exhibited significantly larger skeletal muscles in the breast and leg. Degrees of skeletal muscle hypertrophy and hyperplasia induced by myostatin deletion differed by sex and muscle type. The abdominal fat deposition was dramatically lower in MSTN KO chickens than in wild‐type chickens. Our results demonstrate that the D10A‐Cas9 technical platform can facilitate precise and efficient targeted genome engineering and may broaden the range of applications for genome‐edited chickens in practical industrialization and as animal models of human diseases.

No abstract