González Aitor, Paul Pascale
Aix-Marseille Univ, INSERM U1090, TAGC, Marseille 13288, France.
Comput Struct Biotechnol J. 2024 Nov 17;23:4260-4270. doi: 10.1016/j.csbj.2024.11.019. eCollection 2024 Dec.
Integrating expression quantitative trait loci (eQTL) data with genome-wide association studies (GWAS) enables the discovery of pleiotropic gene regulatory variants that influence a wide range of traits and disease susceptibilities. However, a comprehensive understanding of the distribution of pleiotropic QTLs across the genome and their phenotypic associations remain limited. In this study, we systematically annotated genetic variants associated with both trait variation and gene expression changes, focusing specifically on the unique characteristics of pleiotropic eQTLs. By integrating data from 127 eQTL studies and 417 traits from the IEU Open GWAS Project, we identified 476 pleiotropic eQTL variants affecting two or more distinct traits. Our analysis highlighted 5345 eQTL candidates potentially linked to gene expression changes across 293 GWAS traits. Notably, the 476 pleiotropic eQTLs associated with multiple trait categories were localized within a cumulative 2.5 Mbp genomic region. These pleiotropic eQTLs were enriched in enhancer regions and CTCF loops, influencing a larger number of genes in closer genomic proximity. Our findings reveal that pleiotropic eQTLs are concentrated within a small fraction of the genome and exhibit distinct molecular features. Colocalization results are accessible through an interactive web application and UCSC genome browser tracks at https://gwas2eqtl.tagc.univ-amu.fr/gwas2eqtl, facilitating the exploration of pleiotropic eQTLs and their roles in gene regulation and disease susceptibility.
将表达数量性状基因座(eQTL)数据与全基因组关联研究(GWAS)相结合,能够发现影响多种性状和疾病易感性的多效性基因调控变异。然而,对于多效性QTL在基因组中的分布及其表型关联的全面理解仍然有限。在本研究中,我们系统地注释了与性状变异和基因表达变化相关的遗传变异,特别关注多效性eQTL的独特特征。通过整合来自127项eQTL研究和IEU开放GWAS项目的417个性状的数据,我们鉴定出476个影响两个或更多不同性状的多效性eQTL变异。我们的分析突出了5345个可能与293个GWAS性状的基因表达变化相关的eQTL候选基因。值得注意的是,与多个性状类别相关的476个多效性eQTL定位在累计2.5兆碱基对的基因组区域内。这些多效性eQTL在增强子区域和CTCF环中富集,在更接近的基因组位置影响更多基因。我们的研究结果表明,多效性eQTL集中在基因组的一小部分内,并表现出独特的分子特征。共定位结果可通过交互式网络应用程序和UCSC基因组浏览器轨迹在https://gwas2eqtl.tagc.univ -amu.fr/gwas2eqtl上获取,便于探索多效性eQTL及其在基因调控和疾病易感性中的作用。