Identification of a deep intronic mutation in myostatin causing muscle hypertrophy in cattle provides insights for livestock breeding and potential manipulation of myostatin pre-mRNA in human muscle diseases.
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Supports cattle breeding applications; leaves open myostatin splicing modulation for human muscle disorders.
Myostatin is essential for proper regulation of myogenesis, and inactivation of Myostatin results in muscle hypertrophy. Here, we identified an unexpected mutation in the myostatin gene which is almost fixed in Blonde d'Aquitaine cattle. In skeletal muscle, the mutant allele was highly expressed leading to an abnormal transcript consisting of a 41-bp inclusion and premature termination codons and to residual levels of a correctly spliced transcript. This expression pattern, caused by a leaky intronic mutation with regard to spliceosome activity and its apparent stability with regard to surveillance mechanisms, could contribute to the moderate muscle hypertrophy in this cattle breed. This finding is of importance for genetic counseling for meat quantity and quality in livestock production and possibly to manipulate myostatin pre-mRNA in human muscle diseases.
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Bouyer et al. (2014) studied this question.
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