Moran Colin N, Yang Nan, Bailey Mark E S, Tsiokanos Athanasios, Jamurtas Athanasios, MacArthur Daniel G, North Kathryn, Pitsiladis Yannis P, Wilson Richard H
Institute of Diet, Exercise and Lifestyle (IDEAL) and Division of Molecular Genetics, Faculty of Biomedical & Life Sciences, University of Glasgow, Glasgow, UK.
Eur J Hum Genet. 2007 Jan;15(1):88-93. doi: 10.1038/sj.ejhg.5201724. Epub 2006 Oct 11.
The functional allele (577R) of ACTN3, which encodes human alpha-actinin-3, has been reported to be associated with elite athletic status and with response to resistance training, while the nonfunctional allele (577X) has been proposed as a candidate metabolically thrifty allele. In a study of 992 adolescent Greeks, we show that there is a significant association (P=0.003) between the ACTN3 R577X polymorphism and 40 m sprint time in males that accounts for 2.3% of phenotypic variance, with the 577R allele contributing to faster times in an additive manner. The R577X polymorphism is not associated with other power phenotypes related to 40 m sprint, nor with an endurance phenotype. Furthermore, the polymorphism is not associated with obesity-related phenotypes in our population, suggesting that the 577X allele is not a thrifty allele, and thus the persistence of this null allele must be explained in other terms.
编码人类α-辅肌动蛋白-3的ACTN3功能性等位基因(577R)已被报道与精英运动员身份以及对阻力训练的反应有关,而非功能性等位基因(577X)则被认为是一种潜在的代谢节约型等位基因。在一项针对992名希腊青少年的研究中,我们发现,ACTN3基因R577X多态性与男性40米短跑时间之间存在显著关联(P = 0.003),该多态性可解释2.3%的表型变异,577R等位基因以累加方式使短跑时间更快。R577X多态性与其他与40米短跑相关的力量表型以及耐力表型均无关联。此外,在我们的研究人群中,该多态性与肥胖相关表型也无关联,这表明577X等位基因并非节约型等位基因,因此,这种无效等位基因的持续存在必须从其他方面进行解释。