Asthma-associated genetic variants induce IL33 differential expression through an enhancer-blocking regulatory region

哮喘相关基因变异通过增强子阻断调控区诱导IL33差异表达

阅读:6
作者:Ivy Aneas #,Donna C Decker #,Chanie L Howard,Débora R Sobreira,Noboru J Sakabe,Kelly M Blaine,Michelle M Stein,Cara L Hrusch,Lindsey E Montefiori,Juan Tena,Kevin M Magnaye,Selene M Clay,James E Gern,Daniel J Jackson,Matthew C Altman,Edward T Naureckas,Douglas K Hogarth,Steven R White,Jose Luis Gomez-Skarmeta,Nathan Schoetler,Carole Ober,Anne I Sperling #,Marcelo A Nóbrega #

Abstract

Genome-wide association studies (GWAS) have implicated the IL33 locus in asthma, but the underlying mechanisms remain unclear. Here, we identify a 5 kb region within the GWAS-defined segment that acts as an enhancer-blocking element in vivo and in vitro. Chromatin conformation capture showed that this 5 kb region loops to the IL33 promoter, potentially regulating its expression. We show that the asthma-associated single nucleotide polymorphism (SNP) rs1888909, located within the 5 kb region, is associated with IL33 gene expression in human airway epithelial cells and IL-33 protein expression in human plasma, potentially through differential binding of OCT-1 (POU2F1) to the asthma-risk allele. Our data demonstrate that asthma-associated variants at the IL33 locus mediate allele-specific regulatory activity and IL33 expression, providing a mechanism through which a regulatory SNP contributes to genetic risk of asthma.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。