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Genome-Wide Association Studies of Quantitatively Measured Skin Hair and Eye Pigmentation in Four European Populations

机译:在四个欧洲人群测定的皮肤头发和眼睛色素定量的全基因组关联分析

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摘要

Pigmentation of the skin, hair, and eyes varies both within and between human populations. Identifying the genes and alleles underlying this variation has been the goal of many candidate gene and several genome-wide association studies (GWAS). Most GWAS for pigmentary traits to date have been based on subjective phenotypes using categorical scales. But skin, hair, and eye pigmentation vary continuously. Here, we seek to characterize quantitative variation in these traits objectively and accurately and to determine their genetic basis. Objective and quantitative measures of skin, hair, and eye color were made using reflectance or digital spectroscopy in Europeans from Ireland, Poland, Italy, and Portugal. A GWAS was conducted for the three quantitative pigmentation phenotypes in 176 women across 313,763 SNP loci, and replication of the most significant associations was attempted in a sample of 294 European men and women from the same countries. We find that the pigmentation phenotypes are highly stratified along axes of European genetic differentiation. The country of sampling explains approximately 35% of the variation in skin pigmentation, 31% of the variation in hair pigmentation, and 40% of the variation in eye pigmentation. All three quantitative phenotypes are correlated with each other. In our two-stage association study, we reproduce the association of rs1667394 at the OCA2/HERC2 locus with eye color but we do not identify new genetic determinants of skin and hair pigmentation supporting the lack of major genes affecting skin and hair color variation within Europe and suggesting that not only careful phenotyping but also larger cohorts are required to understand the genetic architecture of these complex quantitative traits. Interestingly, we also see that in each of these four populations, men are more lightly pigmented in the unexposed skin of the inner arm than women, a fact that is underappreciated and may vary across the world.
机译:人群内部和人群之间皮肤,头发和眼睛的色素沉着都不同。鉴定引起这种变异的基因和等位基因已成为许多候选基因和数个全基因组关联研究(GWAS)的目标。迄今为止,大多数针对性状的GWAS都是基于使用分类量表的主观表型。但是皮肤,头发和眼睛的色素沉着不断变化。在这里,我们力求客观,准确地表征这些性状的数量变异,并确定其遗传基础。在爱尔兰,波兰,意大利和葡萄牙的欧洲人中,使用反射率或数字光谱法对皮肤,头发和眼睛的颜色进行了客观和定量的测量。在313,763个SNP位点上的176名女性中,对三种定量色素沉着表型进行了GWAS分析,并试图从同一国家的294名欧洲男性和女性样本中复制最重要的关联。我们发现色素沉着表型沿欧洲遗传分化的轴高度分层。抽样国家解释了大约35%的皮肤色素沉着变化,31%的头发色素沉着变化和40%的眼睛色素沉着变化。这三个定量表型相互关联。在我们的两阶段关联研究中,我们再现了OCA2 / HERC2基因座处的rs166​​7394与眼睛颜色的关联,但我们并未确定皮肤和头发色素沉着的新遗传决定因素,从而支持缺乏影响欧洲内部皮肤和头发颜色变异的主要基因并建议不仅需要仔细的表型分析,而且需要更大的队列研究者才能理解这些复杂的定量性状的遗传结构。有趣的是,我们还发现,在这四个人群中,男性在未暴露的内臂皮肤上的色素较女性少,这一事实并未得到充分重视,并且在全球范围内可能有所不同。

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