Suppr超能文献

南亚裔个体的皮肤和虹膜色素沉着的全基因组关联研究。

A Genome-Wide Association Study of Skin and Iris Pigmentation among Individuals of South Asian Ancestry.

机构信息

Symbiosis School for Liberal Arts, Symbiosis International (Deemed University), Pune, India.

Department of Anthropology, University of Toronto, Ontario, Canada.

出版信息

Genome Biol Evol. 2019 Apr 1;11(4):1066-1076. doi: 10.1093/gbe/evz057.

Abstract

South Asia has a complex history of migrations and is characterized by substantial pigmentary and genetic diversity. For this reason, it is an ideal region to study the genetic architecture of normal pigmentation variation. Here, we present a meta-analysis of two genome-wide association studies (GWASs) of skin pigmentation using skin reflectance (M-index) as a quantitative phenotype. The meta-analysis includes a sample of individuals of South Asian descent living in Canada (N = 348), and a sample of individuals from two caste and four tribal groups from West Maharashtra, India (N = 480). We also present the first GWAS of iris color in South Asian populations. This GWAS was based on quantitative measures of iris color obtained from high-resolution iris pictures. We identified genome-wide significant associations of variants within the well-known gene SLC24A5, including the nonsynonymous rs1426654 polymorphism, with both skin pigmentation and iris color, highlighting the pleiotropic effects of this gene on pigmentation. Variants in the HERC2 gene (e.g., rs12913832) were also associated with iris color and iris heterochromia. Our study emphasizes the usefulness of quantitative methods to study iris color variation. We also identified novel genome-wide significant associations with skin pigmentation and iris color, but we could not replicate these associations due to the lack of independent samples. It will be critical to expand the number of studies in South Asian populations in order to better understand the genetic variation driving the diversity of skin pigmentation and iris color observed in this region.

摘要

南亚拥有复杂的移民历史,其人群特征表现出显著的色素沉着和遗传多样性。正因为如此,南亚是研究正常色素沉着变异遗传结构的理想地区。在这里,我们对两项使用皮肤反射率(M-index)作为定量表型的皮肤色素沉着全基因组关联研究(GWAS)进行了荟萃分析。该荟萃分析包括生活在加拿大的南亚血统个体样本(N=348)和来自印度马哈拉施特拉邦两个种姓和四个部落群体的个体样本(N=480)。我们还报告了南亚人群虹膜颜色的首个全基因组关联研究。该 GWAS 基于从高分辨率虹膜图像中获得的虹膜颜色的定量测量值。我们在众所周知的 SLC24A5 基因内发现了与皮肤色素沉着和虹膜颜色相关的全基因组显著关联的变体,包括非同义 rs1426654 多态性,突出了该基因对色素沉着的多效性影响。HERC2 基因中的变体(例如 rs12913832)也与虹膜颜色和虹膜异色有关。我们的研究强调了使用定量方法研究虹膜颜色变异的有效性。我们还确定了与皮肤色素沉着和虹膜颜色有关的新的全基因组显著关联,但由于缺乏独立样本,我们无法复制这些关联。扩大南亚人群研究的数量对于更好地理解导致该地区观察到的皮肤色素沉着和虹膜颜色多样性的遗传变异至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9b/6456006/e0bac28470d7/evz057f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验