Variation in the uncoupling protein 2 and 3 genes and human performance

被引:15
作者
Dhamrait, Sukhbir S. [1 ,2 ]
Williams, Alun G. [3 ]
Day, Stephen H. [3 ]
Skipworth, James [2 ]
Payne, John R. [2 ]
World, Michael [4 ]
Humphries, Steve E. [2 ]
Montgomery, Hugh E. [5 ,6 ]
机构
[1] Western Sussex Hosp NHS Trust, Dept Cardiol, Worthing BN11 2DH, W Sussex, England
[2] Royal Free & Univ Coll London Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London, England
[3] Manchester Metropolitan Univ, Inst Performance Res, Crewe, England
[4] Selly Oak Hosp, Royal Ctr Def Med HQ, Birmingham B29 6JD, W Midlands, England
[5] UCL Inst Sport Exercise & Hlth, London, England
[6] UCL Inst Hlth & Human Performance, London, England
关键词
uncoupling protein; endurance; genetic variation; single nucleotide polymorphism; gene-environment interaction; FATTY-ACID OXIDATION; BODY-MASS INDEX; SKELETAL-MUSCLE; UCP3; GENE; COMMON POLYMORPHISM; PROTON LEAK; EXPRESSION; EXERCISE; OBESITY; METABOLISM;
D O I
10.1152/japplphysiol.00766.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Dhamrait SS, Williams AG, Day SH, Skipworth J, Payne JR, World M, Humphries SE, Montgomery HE. Variation in the uncoupling protein 2 and 3 genes and human performance. J Appl Physiol 112: 1122-1127, 2012. First published January 12, 2012; doi:10.1152/japplphysiol.00766.2011.-Uncoupling proteins 2 and 3 (UCP2 and UCP3) may negatively regulate mitochondrial ATP synthesis and, through this, influence human physical performance. However, human data relating to both these issues remain sparse. Examining the association of common variants in the UCP3/2 locus with performance phenotypes offers one means of investigation. The efficiency of skeletal muscle contraction, delta efficiency (DE), was assessed by cycle ergometry in 85 young, healthy, sedentary adults both before and after a period of endurance training. Of these, 58 were successfully genotyped for the UCP3-55C>T (rs1800849) and 61 for the UCP2-866G>A (rs659366) variant. At baseline, UCP genotype was unrelated to any physical characteristic, including DE. However, the UCP2-866G>A variant was independently and strongly associated with the DE response to physical training, with UCP2-866A allele carriers exhibiting a greater increase in DE with training (absolute change in DE of -0.2 +/- 3.6% vs. 1.7 +/- 2.8% vs. 2.3 +/- 3.7% for GG vs. GA vs. AA, respectively; P = 0.02 for A allele carriers vs. GG homozygotes). In multivariate analysis, there was a significant interaction between UCP2-866G>A and UCP3-55C>T genotypes in determining changes in DE (adjusted R-2 = 0.137; P value for interaction = 0.003), which was independent of the effect of either single polymorphism or baseline characteristics. In conclusion, common genetic variation at the UCP3/2 gene locus is associated with training-related improvements in DE, an index of skeletal muscle performance. Such effects may be mediated through differences in the coupling of mitochondrial energy transduction in human skeletal muscle, but further mechanistic studies are required to delineate this potential role.
引用
收藏
页码:1122 / 1127
页数:6
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