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东亚人群血液甲基化数量性状基因座分析揭示了其对复杂性状的特定遗传影响。

Analysis of blood methylation quantitative trait loci in East Asians reveals ancestry-specific impacts on complex traits.

机构信息

CAS Key Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.

CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, China.

出版信息

Nat Genet. 2024 May;56(5):846-860. doi: 10.1038/s41588-023-01494-9. Epub 2024 Apr 19.

Abstract

Methylation quantitative trait loci (mQTLs) are essential for understanding the role of DNA methylation changes in genetic predisposition, yet they have not been fully characterized in East Asians (EAs). Here we identified mQTLs in whole blood from 3,523 Chinese individuals and replicated them in additional 1,858 Chinese individuals from two cohorts. Over 9% of mQTLs displayed specificity to EAs, facilitating the fine-mapping of EA-specific genetic associations, as shown for variants associated with height. Trans-mQTL hotspots revealed biological pathways contributing to EA-specific genetic associations, including an ERG-mediated 233 trans-mCpG network, implicated in hematopoietic cell differentiation, which likely reflects binding efficiency modulation of the ERG protein complex. More than 90% of mQTLs were shared between different blood cell lineages, with a smaller fraction of lineage-specific mQTLs displaying preferential hypomethylation in the respective lineages. Our study provides new insights into the mQTL landscape across genetic ancestries and their downstream effects on cellular processes and diseases/traits.

摘要

甲基化定量性状基因座(mQTLs)对于理解 DNA 甲基化变化在遗传易感性中的作用至关重要,但它们在东亚人群(EAs)中尚未得到充分描述。在这里,我们在 3523 名中国个体的全血中鉴定了 mQTLs,并在另外两个队列的 1858 名中国个体中进行了复制。超过 9%的 mQTL 显示出对东亚人群的特异性,有助于精细映射东亚人群特有的遗传关联,如与身高相关的变异。跨 mQTL 热点揭示了导致东亚人群特有的遗传关联的生物学途径,包括 ERG 介导的 233 个跨 mCpG 网络,该网络与造血细胞分化有关,这可能反映了 ERG 蛋白复合物结合效率的调节。超过 90%的 mQTL 存在于不同的血细胞谱系之间,而一小部分谱系特异性 mQTL 则显示出在各自谱系中优先低甲基化。我们的研究为不同遗传背景下的 mQTL 图谱及其对细胞过程和疾病/特征的下游影响提供了新的见解。

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