Mosher Dana S, Quignon Pascale, Bustamante Carlos D, Sutter Nathan B, Mellersh Cathryn S, Parker Heidi G, Ostrander Elaine A
National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS Genet. 2007 May 25;3(5):e79. doi: 10.1371/journal.pgen.0030079. Epub 2007 Apr 30.
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.
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。