Journal
FEBS JOURNAL
Volume 280, Issue 9, Pages 2014-2026Publisher
WILEY
DOI: 10.1111/febs.12225
Keywords
ORMDL3; p300; STAT6; Th2 cytokines; transcription regulation
Categories
Funding
- National Natural Science Foundation of China [30771201, 81072452, 81273281]
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Orosomucoid-like3 (ORMDL3) has been associated with asthma and a series of autoimmune disorders, and is involved in endoplasmic reticulum-mediated inflammatory responses. However, its clinical significance and the molecular mechanism underlying its expression are still largely unclear. To elucidate the mechanisms of human ORMDL3 transcriptional regulation, we cloned a 1.5kb genomic DNA fragment containing the putative promoter region and evaluated its transcriptional activity in a luciferase reporter system by deletion analysis. We identified a 68bp region that functions as a minimal promoter. Bioinformatics analysis predicted that the 64 to 56bp region contained a signal transducer and activator of transcription6 (STAT6) binding site. Electrophoretic mobility shift assay and chromatin immunoprecipitation demonstrated that STAT6 bound to its binding site within the ORMDL3 promoter. STAT6 over-expression or knockdown trans-activated or trans-inhibited, respectively, the ORMDL3 promoter containing the STAT6-binding motif. Treatment with interleukins 4 or 13 increased ORMDL3 promoter activity as well as endogenous ORMDL3 expression. Immunoprecipitation and ChIP/Re-ChIP assays revealed that STAT6 and p300 exist in the same protein complex that binds to the ORMDL3 promoter. Our study confirmed that STAT6 plays important roles in regulating the expression of human ORMDL3 by directly binding to the promoter region, which may shed light on a possible role in various human diseases. Structured digital abstract p300 physically interacts with STAT6 by anti bait coimmunoprecipitation (View Interaction: 1, 2)
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