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正向选择作用于影响 ALDH2 基因表达的欧洲人群中的调控遗传变异。

Positive selection acts on regulatory genetic variants in populations of European ancestry that affect ALDH2 gene expression.

机构信息

Department of Evolutionary Anthropology, Faculty of Life Sciences, University of Vienna, Djerassiplatz 1, 1030, Vienna, Austria.

Department of Medical and Molecular Genetics, Faculty of Life Sciences and Medicine, King's College London, Great Maze Pond, London, SE1 9RT, UK.

出版信息

Sci Rep. 2022 Mar 16;12(1):4563. doi: 10.1038/s41598-022-08588-0.

Abstract

ALDH2 is a key enzyme in alcohol metabolism that protects cells from acetaldehyde toxicity. Using iHS, iSAFE and F statistics, we identified regulatory acting variants affecting ALDH2 gene expression under positive selection in populations of European ancestry. Several SNPs (rs3184504, rs4766578, rs10774625, rs597808, rs653178, rs847892, rs2013002) that function as eQTLs for ALDH2 in various tissues showed evidence of strong positive selection. Very large pairwise F values indicated high genetic differentiation at these loci between populations of European ancestry and populations of other global ancestries. Estimating the timing of positive selection on the beneficial alleles suggests that these variants were recently adapted approximately 3000-3700 years ago. The derived beneficial alleles are in complete linkage disequilibrium with the derived ALDH2 promoter variant rs886205, which is associated with higher transcriptional activity. The SNPs rs4766578 and rs847892 are located in binding sequences for the transcription factor HNF4A, which is an important regulatory element of ALDH2 gene expression. In contrast to the missense variant ALDH2 rs671 (ALDH2*2), which is common only in East Asian populations and is associated with greatly reduced enzyme activity and alcohol intolerance, the beneficial alleles of the regulatory variants identified in this study are associated with increased expression of ALDH2. This suggests adaptation of Europeans to higher alcohol consumption.

摘要

ALDH2 是酒精代谢中的关键酶,可保护细胞免受乙醛毒性的影响。我们使用 iHS、iSAFE 和 F 统计量,在欧洲人群中鉴定出了受正选择影响 ALDH2 基因表达的调控作用变体。几个 SNP(rs3184504、rs4766578、rs10774625、rs597808、rs653178、rs847892、rs2013002)在各种组织中作为 ALDH2 的 eQTL 发挥作用,表现出强烈正选择的证据。非常大的成对 F 值表明,欧洲人群和其他全球人群之间这些位点的遗传分化很高。对有益等位基因的正选择时间的估计表明,这些变体大约在 3000-3700 年前被最近适应。衍生的有益等位基因与衍生的 ALDH2 启动子变体 rs886205 完全连锁不平衡,后者与更高的转录活性相关。SNP rs4766578 和 rs847892 位于转录因子 HNF4A 的结合序列中,HNF4A 是 ALDH2 基因表达的重要调节元件。与仅在东亚人群中常见且与酶活性大大降低和酒精不耐受相关的错义变体 ALDH2 rs671(ALDH2*2)不同,本研究中鉴定的调控变体的有益等位基因与 ALDH2 的表达增加相关。这表明欧洲人适应了更高的酒精摄入量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6362/8927298/6b9c6446ed23/41598_2022_8588_Fig1_HTML.jpg

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