Castillo Joseph J, Hazlett Zachary S, Orlando Robert A, Garver William S
Department of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Department of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Gene. 2017 Sep 5;627:412-419. doi: 10.1016/j.gene.2017.07.002. Epub 2017 Jul 4.
It is generally accepted that the selection of gene variants during human evolution optimized energy metabolism that now interacts with our obesogenic environment to increase the prevalence of obesity. The purpose of this study was to perform a global evolutionary and metabolic analysis of human obesity gene risk variants (110 human obesity genes with 127 nearest gene risk variants) identified using genome-wide association studies (GWAS) to enhance our knowledge of early and late genotypes. As a result of determining the mean frequency of these obesity gene risk variants in 13 available populations from around the world our results provide evidence for the early selection of ancestral risk variants (defined as selection before migration from Africa) and late selection of derived risk variants (defined as selection after migration from Africa). Our results also provide novel information for association of these obesity genes or encoded proteins with diverse metabolic pathways and other human diseases. The overall results indicate a significant differential evolutionary pattern for the selection of obesity gene ancestral and derived risk variants proposed to optimize energy metabolism in varying global environments and complex association with metabolic pathways and other human diseases. These results are consistent with obesity genes that encode proteins possessing a fundamental role in maintaining energy metabolism and survival during the course of human evolution.
人们普遍认为,人类进化过程中基因变异的选择优化了能量代谢,而如今这种能量代谢与我们的致肥胖环境相互作用,增加了肥胖的患病率。本研究的目的是对通过全基因组关联研究(GWAS)确定的人类肥胖基因风险变异(110个人类肥胖基因,带有127个最接近的基因风险变异)进行全面的进化和代谢分析,以增进我们对早期和晚期基因型的了解。通过测定全球13个现有群体中这些肥胖基因风险变异的平均频率,我们的研究结果为祖先风险变异(定义为从非洲迁移之前的选择)的早期选择和衍生风险变异(定义为从非洲迁移之后的选择)的晚期选择提供了证据。我们的研究结果还为这些肥胖基因或编码蛋白与多种代谢途径及其他人类疾病的关联提供了新信息。总体结果表明,在不同全球环境中为优化能量代谢而选择肥胖基因祖先和衍生风险变异存在显著的差异进化模式,且与代谢途径及其他人类疾病存在复杂关联。这些结果与在人类进化过程中编码对维持能量代谢和生存具有基本作用的蛋白质的肥胖基因一致。