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Publication : SUMOylation of ROR-γt inhibits IL-17 expression and inflammation via HDAC2.

First Author  Singh AK Year  2018
Journal  Nat Commun Volume  9
Issue  1 Pages  4515
PubMed ID  30375383 Mgi Jnum  J:268526
Mgi Id  MGI:6267977 Doi  10.1038/s41467-018-06924-5
Citation  Singh AK, et al. (2018) SUMOylation of ROR-gammat inhibits IL-17 expression and inflammation via HDAC2. Nat Commun 9(1):4515
abstractText  Dysregulated ROR-gammat-mediated IL-17 transcription is central to the pathogenesis of several inflammatory disorders, yet the molecular mechanisms that govern the transcription factor activity of ROR-gammat in the regulation of IL-17 are not fully defined. Here we show that SUMO-conjugating enzyme Ubc9 interacts with a conserved GKAE motif in ROR-gammat to induce SUMOylation of ROR-gammat and suppress IL-17 expression. Th17 cells expressing SUMOylation-defective ROR-gammat are highly colitogenic upon transfer to Rag1(-/-) mice. Mechanistically, SUMOylation of ROR-gammat facilitates the binding of HDAC2 to the IL-17 promoter and represses IL-17 transcription. Mice with conditional deletion of HDAC2 in CD4(+) T cells have elevated IL-17 expression and severe colitis. The identification of the Ubc9/ROR-gammat/HDAC2 axis that governs IL-17 expression may open new venues for the development of therapeutic measures for inflammatory disorders.
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