Cutting Edge: Hypoxia-Induced Ubc9 Promoter Hypermethylation Regulates IL-17 Expression in Ulcerative Colitis.
Ritesh KumarAmir Kumar SinghPetro StarokadomskyyMaowu LuoArianne L TheissEzra BursteinK VenuprasadPublished in: Journal of immunology (Baltimore, Md. : 1950) (2021)
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.
Keyphrases
- ulcerative colitis
- poor prognosis
- transcription factor
- dna methylation
- crispr cas
- oxidative stress
- gene expression
- binding protein
- end stage renal disease
- chronic kidney disease
- long non coding rna
- endothelial cells
- type diabetes
- induced apoptosis
- metabolic syndrome
- ejection fraction
- peritoneal dialysis
- prognostic factors
- signaling pathway
- adipose tissue
- endoplasmic reticulum stress
- patient reported