Wan Jing, van Ouwerkerk Antoinette, Mouren Jean-Christophe, Heredia Carla, Pradel Lydie, Ballester Benoit, Andrau Jean-Christophe, Spicuglia Salvatore
Aix-Marseille University, INSERM, TAGC, UMR 1090 Marseille, France.
Equipe Labellisée LIGUE, 2023 Marseille, France.
Nucleic Acids Res. 2025 Feb 8;53(4). doi: 10.1093/nar/gkae1270.
There is growing evidence that a wide range of human diseases and physiological traits are influenced by genetic variation of cis-regulatory elements. We and others have shown that a subset of promoter elements, termed Epromoters, also function as enhancer regulators of distal genes. This opens a paradigm in the study of regulatory variants, as single nucleotide polymorphisms (SNPs) within Epromoters might influence the expression of several (distal) genes at the same time, which could disentangle the identification of disease-associated genes. Here, we built a comprehensive resource of human Epromoters using newly generated and publicly available high-throughput reporter assays. We showed that Epromoters display intrinsic and epigenetic features that distinguish them from typical promoters. By integrating Genome-Wide Association Studies (GWAS), expression Quantitative Trait Loci (eQTLs) and 3D chromatin interactions, we found that regulatory variants at Epromoters are concurrently associated with more disease and physiological traits, as compared with typical promoters. To dissect the regulatory impact of Epromoter variants, we evaluated their impact on regulatory activity by analyzing allelic-specific high-throughput reporter assays and provided reliable examples of pleiotropic Epromoters. In summary, our study represents a comprehensive resource of regulatory variants supporting the pleiotropic role of Epromoters.
越来越多的证据表明,多种人类疾病和生理特征受到顺式调控元件遗传变异的影响。我们和其他人已经表明,一部分启动子元件,称为Epromoters,也作为远端基因的增强子调节因子发挥作用。这为调控变异的研究开辟了一种范式,因为Epromoters内的单核苷酸多态性(SNP)可能同时影响多个(远端)基因的表达,这可能会使疾病相关基因的鉴定变得复杂。在这里,我们利用新生成的和公开可用的高通量报告基因检测构建了一个全面的人类Epromoters资源。我们表明,Epromoters具有内在和表观遗传特征,使其与典型启动子区分开来。通过整合全基因组关联研究(GWAS)、表达数量性状位点(eQTL)和三维染色质相互作用,我们发现与典型启动子相比,Epromoters处的调控变异与更多的疾病和生理特征同时相关。为了剖析Epromoter变异的调控影响,我们通过分析等位基因特异性高通量报告基因检测评估了它们对调控活性的影响,并提供了多效性Epromoters的可靠实例。总之,我们的研究代表了一个支持Epromoters多效性作用的调控变异综合资源。