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欧洲裔人群中晒黑表型的全基因组关联研究。

Genome-wide association study of tanning phenotype in a population of European ancestry.

作者信息

Nan Hongmei, Kraft Peter, Qureshi Abrar A, Guo Qun, Chen Constance, Hankinson Susan E, Hu Frank B, Thomas Gilles, Hoover Robert N, Chanock Stephen, Hunter David J, Han Jiali

机构信息

Channing Laboratory, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

J Invest Dermatol. 2009 Sep;129(9):2250-7. doi: 10.1038/jid.2009.62. Epub 2009 Apr 2.

Abstract

We conducted a multistage genome-wide association study (GWAS) of tanning response after exposure to sunlight in over 9,000 men and women of European ancestry who live in the United States. An initial analysis of 528,173 single-nucleotide polymorphisms (SNPs) genotyped on 2,287 women identified LOC401937 (rs966321) on chromosome 1 as a novel locus highly associated with tanning ability, and we confirmed this association in 870 women controls from a skin cancer case-control study with joint P-value=1.6 x 10(-9). We further genotyped this SNP in two subsequent replication studies (one with 3,750 women and the other with 2,405 men). This association was not replicated in either of these two studies. We found that several SNPs reaching the genome-wide significance level are located in or adjacent to the loci previously known as pigmentation genes: MATP, IRF4, TYR, OCA2, and MC1R. Overall, these tanning ability-related loci are similar to the hair color-related loci previously reported in the GWAS of hair color.

摘要

我们对9000多名居住在美国的欧洲裔男女进行了一项关于阳光照射后晒黑反应的多阶段全基因组关联研究(GWAS)。对2287名女性进行的528173个单核苷酸多态性(SNP)的初步基因分型分析确定,1号染色体上的LOC401937(rs966321)是一个与晒黑能力高度相关的新位点,并且我们在一项皮肤癌病例对照研究的870名女性对照中证实了这种关联,联合P值 = 1.6×10^(-9)。我们在随后的两项重复研究中对该SNP进行了进一步基因分型(一项研究有3750名女性,另一项研究有2405名男性)。在这两项研究中均未重复出这种关联。我们发现,几个达到全基因组显著性水平的SNP位于先前已知的色素沉着基因位点内或其附近:MATP、IRF4、TYR、OCA2和MC1R。总体而言,这些与晒黑能力相关的位点与先前在头发颜色GWAS中报道的与头发颜色相关的位点相似。

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本文引用的文献

2
Two newly identified genetic determinants of pigmentation in Europeans.
Nat Genet. 2008 Jul;40(7):835-7. doi: 10.1038/ng.160. Epub 2008 May 18.
3
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
PLoS Genet. 2008 May 16;4(5):e1000074. doi: 10.1371/journal.pgen.1000074.
4
A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.
Am J Hum Genet. 2008 Feb;82(2):424-31. doi: 10.1016/j.ajhg.2007.11.005. Epub 2008 Jan 24.
6
Genetic determinants of hair, eye and skin pigmentation in Europeans.
Nat Genet. 2007 Dec;39(12):1443-52. doi: 10.1038/ng.2007.13. Epub 2007 Oct 21.
7
A second generation human haplotype map of over 3.1 million SNPs.
Nature. 2007 Oct 18;449(7164):851-61. doi: 10.1038/nature06258.
8
Replicating genotype-phenotype associations.
Nature. 2007 Jun 7;447(7145):655-60. doi: 10.1038/447655a.
10
A prospective study of plasma prolactin concentrations and risk of premenopausal and postmenopausal breast cancer.
J Clin Oncol. 2007 Apr 20;25(12):1482-8. doi: 10.1200/JCO.2006.07.6356. Epub 2007 Mar 19.

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