109 / 2024-10-29 16:32:02
Comprehensive mapping of genetic variation at Epromoters reveals pleiotropic association with multiple disease traits
Regulatory elements,enhancer,promoter,human disease
摘要待审
WanJing / TAGC-INSERM; Aix-Marseille University
SpicugliaSalvatore / Aix-Marseille University, INSERM, TAGC, UMR 1090, Marseille, France.
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.
重要日期
  • 会议日期

    10月31日

    2024

    11月03日

    2024

  • 11月03日 2024

    注册截止日期

主办单位
崖州湾国家实验室
华中农业大学
浙江大学
中国遗传学会
中国遗传学会三维基因组学专委会
承办单位
中国生物信息学基因组信息学专委会
中国遗传学会表观遗传分会
中国细胞生物学学会染色质生物学分会
联系方式
历届会议
移动端
在手机上打开
小程序
打开微信小程序
客服
扫码或点此咨询