| Literature DB >> 33504619 |
Ritesh Kumar1,2, Amir Kumar Singh1,2, Petro Starokadomskyy1, Weibo Luo3, Arianne L Theiss4, Ezra Burstein1,5, K Venuprasad6,2.
Abstract
Dysregulated IL-17 expression is central to the pathogenesis of several inflammatory disorders, including ulcerative colitis. We have shown earlier that SUMOylation of ROR-γt, the transcription factor for IL-17, regulates colonic inflammation. In this study, we show that the expression of Ubc9, the E2 enzyme that targets ROR-γt for SUMOylation, is significantly reduced in the colonic mucosa of ulcerative colitis patients. Mechanistically, we demonstrate that hypoxia-inducible factor 1α (HIF-1α) binds to a CpG island within the Ubc9 gene promoter, resulting in its hypermethylation and reduced Ubc9 expression. CRISPR-Cas9-mediated inhibition of HIF-1α normalized Ubc9 and attenuated IL-17 expression in Th17 cells and reduced diseases severity in Rag1 -/- mice upon adoptive transfer. Collectively, our study reveals a novel epigenetic mechanism of regulation of ROR-γt that could be exploited in inflammatory diseases.Entities:
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Year: 2021 PMID: 33504619 PMCID: PMC7889719 DOI: 10.4049/jimmunol.2000015
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422