bioRxivGenomicsPreprint
Asthma-associated variants induce IL33 differential expression through a novel regulatory region
Ivy AneasiD, Donna C. Decker, Chanie L. Howard, Débora R. SobreiraiD, Noboru J. SakabeiD, Kelly M. BlaineiD, Michelle M. SteiniD, Cara Lynn Hrusch, Lindsey E. MontefioriiD, Juan J. TenaiD, Kevin M. MagnayeiD, Selene M. ClayiD, James E. GerniD, Daniel J. JacksoniD, Matthew C. AltmaniD, Edward T. NaureckasiD, D. Kyle HogarthiD, Steven R. WhiteiD, José Luis Gómez-SkármetaiD, Nathan SchoettleriD, Carole OberiD, Anne I. SperlingiD, Marcelo A. NóbregaiD
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 a strong regulatory element in vivo and in vitro. Chromatin conformation capture showed that this 5 kb region loops to the IL33 promoter, potentially regulating its expression. Supporting this notion, we show that genotype at an asthma-associated 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 novel mechanism through which a regulatory SNP contributes to genetic risk of asthma.
- organism: human
- assay: bulk RNA-seq
- research focus: differential expression
- approach: statistical model
- Citations
- 0
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