Adipose tissue eQTL meta-analysis highlights the contribution of allelic heterogeneity to gene expression regulation and cardiometabolic traits.

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Tác giả: Michael Boehnke, Lori L Bonnycastle, K Alaine Broadaway, Sarah M Brotman, Francis S Collins, Kevin W Currin, Julia S El-Sayed Moustafa, Michael R Erdos, Lilian Fernandes Silva, Li Guan, Anne U Jackson, Heikki A Koistinen, Johanna Kuusisto, Markku Laakso, Timo A Lakka, Michael I Love, Karen L Mohlke, Narisu Narisu, Anniina Oravilahti, Päivi Pajukanta, Stephen C J Parker, Chelsea K Raulerson, Yasrab Raza, Amy L Roberts, Laura J Scott, Kerrin S Small, Heather M Stringham, Max Tomlinson, Jaakko Tuomilehto, Swarooparani Vadlamudi, Dongmeng Wang, Ryan Welch, Tingfen Yan, Xinyu Yan

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: United States : Nature genetics , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 253885

 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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