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肿瘤坏死因子-α启动子单核苷酸多态性是人类祖先的标志。

TNF-alpha promoter single nucleotide polymorphisms are markers of human ancestry.

作者信息

Baena A, Leung J Y, Sullivan A D, Landires I, Vasquez-Luna N, Quiñones-Berrocal J, Fraser P A, Uko G P, Delgado J C, Clavijo O P, Thim S, Meshnick S R, Nyirenda T, Yunis E J, Goldfeld A E

机构信息

Center for Blood Research, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Genes Immun. 2002 Dec;3(8):482-7. doi: 10.1038/sj.gene.6363898.

Abstract

We present a map of single nucleotide polymorphisms (SNPs) in the human tumor necrosis factor (TNF)-alpha promoter based upon exploratory sequencing of 333 human TNF-alpha gene promoters from individuals of distinct ancestral backgrounds. We detect 10 TNF-alpha promoter SNPs that occur with distinct frequencies in populations of different ancestry. Consistent with these findings, we show that two TNF-alpha SNPs, the -243 SNP and the -856 SNP, are the first SNP markers of a sub-Saharan African-derived extended haplotype and an Amerindian HLA haplotype, respectively. Comparisons of TNF-alpha promoter SNP allele frequencies can thus help elucidate variation of HLA haplotypes and their distribution among existing ethnic groups and shed light into the history of human populations.

摘要

我们基于对来自不同祖先背景个体的333个人类肿瘤坏死因子(TNF)-α基因启动子的探索性测序,呈现了人类TNF-α启动子中的单核苷酸多态性(SNP)图谱。我们检测到10个TNF-α启动子SNP,它们在不同祖先的人群中出现频率各异。与这些发现一致,我们表明两个TNF-α SNP,即-243 SNP和-856 SNP,分别是源自撒哈拉以南非洲的扩展单倍型和美洲印第安人HLA单倍型的首个SNP标记。因此,TNF-α启动子SNP等位基因频率的比较有助于阐明HLA单倍型的变异及其在现有族群中的分布,并为人类种群历史提供线索。

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