| Literature DB >> 25937118 |
Lihan Chen1, Weini Li1, Weiyi Qiu1, Wen Ren1, Qincao Li1, Baiyu Han1, Lei Zhou1, Long Cheng2, Hao Zhang3, Qinong Ye4.
Abstract
The transcription factor estrogen receptor β (ERβ) plays roles in the central nervous, endocrine, cardiovascular, and immune systems. ERβ can be SUMOylated. However, the underlying mechanism remains unclear. Here, we show that RSRC1/SRrp53 interacts with ERβ and SUMOylation of RSRC1 is required for regulation of PIAS1-mediated ERβ SUMOylation. RSRC1 promotes ERβ SUMOylation through enhanced interaction between ERβ and PIAS1. RSRC1 represses ERβ transcriptional activity through regulation of ERβ SUMOylation. By establishing RSRC1 as a novel cofactor for SUMOylation, our data provide insight into regulation of ERβ SUMOylation and indicate that SUMOylation of one protein can regulate another protein SUMOylation.Entities:
Keywords: ERβ; PIAS1; RSRC1/SRrp53; SUMOylation; Transcriptional activity
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Year: 2015 PMID: 25937118 DOI: 10.1016/j.febslet.2015.04.035
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124