表达数量性状基因座
生物
全基因组关联研究
数量性状位点
遗传学
基因
基因座(遗传学)
遗传关联
等位基因
基因表达调控
单核苷酸多态性
基因型
作者
Sarah M. Brotman,Julia S. El-Sayed Moustafa,Li Guan,K. Alaine Broadaway,Dongmeng Wang,Anne Jackson,Ryan Welch,Kevin W. Currin,Max Tomlinson,Swarooparani Vadlamudi,Heather M. Stringham,Amy L. Roberts,Timo A. Lakka,Anniina Oravilahti,Lilian Fernandes Silva,Narisu Narisu,Michael R. Erdos,Tingfen Yan,Lori L. Bonnycastle,Chelsea K. Raulerson
出处
期刊:Nature Genetics
[Springer Nature]
日期:2025-01-01
卷期号:57 (1): 180-192
被引量:13
标识
DOI:10.1038/s41588-024-01982-6
摘要
Complete characterization of the genetic effects on gene expression is needed to elucidate tissue biology and the etiology of complex traits. In the present study, we analyzed 2,344 subcutaneous adipose tissue samples and identified 34,774 conditionally distinct expression quantitative trait locus (eQTL) signals at 18,476 genes. Over half of eQTL genes exhibited at least two eQTL signals. Compared with primary eQTL signals, nonprimary eQTL signals had lower effect sizes, lower minor allele frequencies and less promoter enrichment; they corresponded to genes with higher heritability and higher tolerance for loss of function. Colocalization of eQTLs with genome-wide association study (GWAS) signals for 28 cardiometabolic traits identified 1,835 genes. Inclusion of nonprimary eQTL signals increased discovery of colocalized GWAS-eQTL signals by 46%. Furthermore, 21 genes with ≥2 colocalized GWAS-eQTL signals showed a mediating gene dosage effect on the GWAS trait. Thus, expanded eQTL identification reveals more mechanisms underlying complex traits and improves understanding of the complexity of gene expression regulation.
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