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肌生成抑制素基因的突变会增加杂合子犬的肌肉量并提高其赛跑成绩。

A mutation in the myostatin gene increases muscle mass and enhances racing performance in heterozygote dogs.

作者信息

Mosher Dana S, Quignon Pascale, Bustamante Carlos D, Sutter Nathan B, Mellersh Cathryn S, Parker Heidi G, Ostrander Elaine A

机构信息

National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.

出版信息

PLoS Genet. 2007 May 25;3(5):e79. doi: 10.1371/journal.pgen.0030079. Epub 2007 Apr 30.

Abstract

Double muscling is a trait previously described in several mammalian species including cattle and sheep and is caused by mutations in the myostatin (MSTN) gene (previously referred to as GDF8). Here we describe a new mutation in MSTN found in the whippet dog breed that results in a double-muscled phenotype known as the "bully" whippet. Individuals with this phenotype carry two copies of a two-base-pair deletion in the third exon of MSTN leading to a premature stop codon at amino acid 313. Individuals carrying only one copy of the mutation are, on average, more muscular than wild-type individuals (p = 7.43 x 10(-6); Kruskal-Wallis Test) and are significantly faster than individuals carrying the wild-type genotype in competitive racing events (Kendall's nonparametric measure, tau = 0.3619; p approximately 0.00028). These results highlight the utility of performance-enhancing polymorphisms, marking the first time a mutation in MSTN has been quantitatively linked to increased athletic performance.

摘要

双肌性状先前已在包括牛和羊在内的几种哺乳动物中被描述过,它是由肌肉生长抑制素(MSTN)基因(先前称为GDF8)的突变引起的。在此,我们描述了在惠比特犬品种中发现的MSTN基因的一种新突变,该突变导致了一种被称为“恶霸”惠比特的双肌表型。具有这种表型的个体在MSTN基因的第三个外显子中携带两个碱基对缺失的拷贝,导致在氨基酸313处出现提前终止密码子。仅携带一个突变拷贝的个体平均比野生型个体肌肉更发达(p = 7.43×10⁻⁶;Kruskal - Wallis检验),并且在竞技比赛中比携带野生型基因型的个体显著更快(肯德尔非参数度量,tau = 0.3619;p约为0.00028)。这些结果突出了性能增强多态性的效用,这标志着MSTN基因的突变首次被定量地与运动成绩提高联系起来。

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