Jonnalagadda Manjari, Bharti Neeraj, Patil Yatish, Ozarkar Shantanu, K Sunitha Manjari, Joshi Rajendra, Norton Heather
Symbiosis School for Liberal Arts (SSLA), Symbiosis International University (SIU), Pune, 411014, India.
HPC-MBA Group, Centre for Development of Advanced Computing, Pune, 411007, India.
Am J Hum Biol. 2017 Sep 10;29(5). doi: 10.1002/ajhb.23012. Epub 2017 Apr 24.
Skin pigmentation is a polygenic trait showing wide phenotypic variations among global populations. While numerous pigmentation genes have been identified to be under positive selection among European and East populations, genes contributing to phenotypic variation in skin pigmentation within and among South Asian populations are still poorly understood. The present study uses data from the Phase 3 of the 1000 genomes project focusing on two South Asian populations-GIH (Gujarati Indian from Houston, Texas) and ITU (Indian Telugu from UK), so as to decode the genetic architecture involved in adaptation to ultraviolet radiation in South Asian populations.
Statistical tests included were (1) tests to identify deviations of the Site Frequency Spectrum (SFS) from neutral expectations (Tajima's D, Fay and Wu's H and Fu and Li's D* and F*), (2) tests focused on the identification of high-frequency haplotypes with extended linkage disequilibrium (iHS and Rsb), and (3) tests based on genetic differentiation between populations (LSBL).
Twenty-two pigmentation genes fall in the top 1% for at least one statistic in the GIH population, 5 of which (LYST, OCA2, SLC24A5, SLC45A2, and TYR) have been previously associated with normal variation in skin, hair, or eye color. In comparison, 17 genes fall in the top 1% for at least one statistic in the ITU population. Twelve loci which are identified as outliers in the ITU scan were also identified in the GIH population.
These results suggest that selection may have affected these loci broadly across the region.
皮肤色素沉着是一种多基因性状,在全球人群中表现出广泛的表型变异。虽然已经确定许多色素沉着基因在欧洲和东亚人群中受到正选择,但对于导致南亚人群内部和之间皮肤色素沉着表型变异的基因仍知之甚少。本研究使用来自千人基因组计划第三阶段的数据,重点关注两个南亚人群——GIH(来自德克萨斯州休斯顿的古吉拉特印度人)和ITU(来自英国的印度泰卢固人),以解码南亚人群适应紫外线辐射所涉及的遗传结构。
所包含的统计检验包括:(1)识别位点频率谱(SFS)与中性预期偏差的检验( Tajima's D、Fay和Wu's H以及Fu和Li's D和F);(2)专注于识别具有扩展连锁不平衡的高频单倍型的检验(iHS和Rsb);(3)基于人群间遗传分化的检验(LSBL)。
在GIH人群中,22个色素沉着基因在至少一项统计中位列前1%,其中5个基因(LYST、OCA2、SLC24A5、SLC45A2和TYR)先前已与皮肤、头发或眼睛颜色的正常变异相关。相比之下,在ITU人群中,17个基因在至少一项统计中位列前1%。在ITU扫描中被确定为异常值的12个位点在GIH人群中也被确定。
这些结果表明,选择可能在整个区域广泛影响了这些位点。