与动脉粥样硬化和炎症相关的y染色体遗传变异。

A. Lusis
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引用次数: 3

摘要

人类全基因组关联研究(GWAS)已经确定了100多个与冠状动脉疾病(CAD)有关的位点,但这些研究在很大程度上忽略了Y染色体(chr)在本期《ATVB》中,Eales等人在英国生物银行研究的1229133名男性中发现了Y染色体遗传变异与CAD之间的显著关联。他们通过识别与变异相关的表观遗传和基因表达模式对这一发现进行了追踪,并提出证据表明,Y chr基因无处不在地转录含有四肽重复序列的Y-linked,一种组蛋白去甲基化酶,可能通过其在巨噬细胞中的炎症作用发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Y-Chromosome Genetic Variation Associated With Atherosclerosis and Inflammation.
Human GWAS (Genome-Wide Association Studies) have identified over 100 loci contributing to coronary artery disease (CAD), but such studies have largely ignored the Y chromosome (chr).1 In this issue of ATVB, Eales et al2 have identified a significant association between genetic variants on the Y chr and CAD in 129 133 men from the UK Biobank study. They followed up on this finding by identifying epigenetic and gene expression patterns associated with the variants and they present evidence that the Y chr gene ubiquitously transcribed tetratricopeptide repeat-containing Y-linked, a histone demethylase, may contribute through its inflammatory effects in macrophages.
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