Department of Health and Kinesiology, Texas A&M University, College Station, TX, United States of America.
PLoS One. 2019 Apr 29;14(4):e0216155. doi: 10.1371/journal.pone.0216155. eCollection 2019.
The purpose of this study was to determine the estimated mutation age and conservation of single-nucleotide polymorphisms (SNPs) associated with physical activity (PA) in humans. All human SNPs found to be significantly associated with PA levels in the literature were cross-referenced with the National Heart, Lung, and Blood Institute's Grand Opportunity Exome Sequencing Project to find estimated African-American (AA) and European-American (EA) mutation age. As a secondary measure of mutation age, SNPs were searched for in Hawk's mutation age prediction database which utilizes linkage equilibrium. To determine conservation among hominids, all SNPs were searched in the University of California, Santa Cruz Genome Browser, which contains Neanderthal and chimpanzee reference genomes. Six of the 104 SNPs associated with PA regulation were exon-located missense variants found in IFNAR2, PPARGC1A, PML, CTBP2, IL5RA, and APOE genes. The remaining 98 SNPs were located in non-protein coding regions. Average AA and EA estimated mutation age of the exon-located SNPs were 478.4 ± 327.5 kya and 542.1 ± 369.4 kya, respectively. There were four selective sweeps (suggestive of strong positive selection) of SNPs in humans when compared to Neanderthal or chimpanzee genomes. Exon-located PA candidate SNPs are older than the hypothesized emergence of anatomically modern humans. However, 95% of PA associated SNPs are found in intron and intergenic location. Across all SNPs, there seems to be a high level of conservation of alleles between humans, Neanderthals, and chimpanzees. However, the presence of four selective sweeps suggests there were selection pressures or drift unique to Homo sapiens that influenced the development of mutations associated with PA regulation.
本研究旨在确定与人类体力活动(PA)相关的单核苷酸多态性(SNP)的估计突变年龄和保守性。文献中发现与 PA 水平显著相关的所有人类 SNP 都与国家心肺血液研究所的大机遇外显子测序计划进行了交叉引用,以找到估计的非裔美国人(AA)和欧洲裔美国人(EA)的突变年龄。作为突变年龄的次要衡量标准,利用连锁平衡在 Hawk 的突变年龄预测数据库中搜索了 SNPs。为了确定在人科动物中的保守性,所有 SNP 都在加利福尼亚大学圣克鲁斯基因组浏览器中进行了搜索,其中包含尼安德特人和黑猩猩参考基因组。与 PA 调节相关的 104 个 SNP 中有 6 个是位于外显子的错义变异,位于 IFNAR2、PPARGC1A、PML、CTBP2、IL5RA 和 APOE 基因中。其余 98 个 SNP 位于非蛋白编码区。位于外显子的 SNP 的平均 AA 和 EA 估计突变年龄分别为 478.4 ± 327.5 kya 和 542.1 ± 369.4 kya。与尼安德特人和黑猩猩基因组相比,人类有 4 个 SNP 发生了选择性清除(提示存在强烈的正选择)。位于外显子的 PA 候选 SNP 比假设的解剖学上现代人类的出现要古老。然而,95%的与 PA 相关的 SNP 位于内含子和基因间区。在所有 SNP 中,人类、尼安德特人和黑猩猩之间的等位基因似乎具有高度的保守性。然而,存在 4 个选择性清除表明,存在影响与 PA 调节相关的突变发展的独特的人类选择压力或漂变。