Department of Kinesiology, School of Public Health, University of Maryland, College Park, MD, USA.
Med Sci Sports Exerc. 2012 May;44(5):809-17. doi: 10.1249/MSS.0b013e31824f28b6.
This review of the exercise genomics literature emphasizes the highest quality articles published in 2011. Given this emphasis on the best publications, only a small number of published articles are reviewed. One study found that physical activity levels were significantly lower in patients with mitochondrial DNA mutations compared with controls. A two-stage fine-mapping follow-up of a previous linkage peak found strong associations between sequence variation in the activin A receptor, type-1B (ACVRIB) gene and knee extensor strength, with rs2854464 emerging as the most promising candidate polymorphism. The association of higher muscular strength with the rs2854464 A allele was confirmed in two separate cohorts. A study using a combination of transcriptomic and genomic data identified a comprehensive map of the transcriptomic features important for aerobic exercise training-induced improvements in maximal oxygen consumption, but no genetic variants derived from candidate transcripts were associated with trainability. A large-scale de novo meta-analysis confirmed that the effect of sequence variation in the fat mass and obesity-associated (FTO) gene on the risk of obesity differs between sedentary and physically active adults. Evidence for gene-physical activity interactions on type 2 diabetes risk was found in two separate studies. A large study of women found that physical activity modified the effect of polymorphisms in the lipoprotein lipase (LPL), hepatic lipase (LIPC), and cholesteryl ester transfer protein (CETP) genes, identified in previous genome-wide association study reports, on HDL cholesterol. We conclude that a strong exercise genomics corpus of evidence would not only translate into powerful genomic predictors but also have a major effect on exercise biology and exercise behavior research.
这篇关于运动基因组学文献的综述强调了 2011 年发表的最高质量的文章。鉴于对最佳出版物的重视,只有少数已发表的文章被审查。一项研究发现,与对照组相比,线粒体 DNA 突变患者的体力活动水平明显较低。一项对先前连锁峰的两阶段精细映射随访发现,激活素 A 受体、1B 型(ACVRIB)基因中的序列变异与膝伸肌力量之间存在强烈关联,rs2854464 作为最有前途的候选多态性出现。rs2854464 A 等位基因与更高肌肉力量的关联在两个独立队列中得到了证实。一项使用转录组和基因组数据组合的研究确定了有氧运动训练诱导最大耗氧量改善的转录组特征的综合图谱,但没有来自候选转录本的遗传变异与可训练性相关。一项大规模的从头元分析证实,序列变异在肥胖相关基因(FTO)上对肥胖风险的影响在久坐和活跃的成年人之间存在差异。两项独立的研究发现了与 2 型糖尿病风险相关的基因-体力活动相互作用的证据。一项对女性的大型研究发现,体力活动改变了脂蛋白脂肪酶(LPL)、肝脂肪酶(LIPC)和胆固醇酯转移蛋白(CETP)基因多态性的影响,这些多态性在先前的全基因组关联研究报告中被确定为高密度脂蛋白胆固醇。我们的结论是,一个强大的运动基因组学证据库不仅会转化为强大的基因组预测因子,而且会对运动生物学和运动行为研究产生重大影响。