| Literature DB >> 29628309 |
Wei-Wei Gao1, Rong-Quan Xiao1, Wen-Juan Zhang1, Yi-Ren Hu2, Bing-Ling Peng1, Wen-Juan Li1, Yao-Hui He1, Hai-Feng Shen1, Jian-Cheng Ding1, Qi-Xuan Huang1, Tian-Yi Ye1, Ying Li1, Zhi-Ying Liu1, Rong Ding1, Michael G Rosenfeld2, Wen Liu3.
Abstract
Whereas the actions of enhancers in gene transcriptional regulation are well established, roles of JmjC-domain-containing proteins in mediating enhancer activation remain poorly understood. Here, we report that recruitment of the JmjC-domain-containing protein 6 (JMJD6) to estrogen receptor alpha (ERα)-bound active enhancers is required for RNA polymerase II recruitment and enhancer RNA production on enhancers, resulting in transcriptional pause release of cognate estrogen target genes. JMJD6 is found to interact with MED12 in the mediator complex to regulate its recruitment. Unexpectedly, JMJD6 is necessary for MED12 to interact with CARM1, which methylates MED12 at multiple arginine sites and regulates its chromatin binding. Consistent with its role in transcriptional activation, JMJD6 is required for estrogen/ERα-induced breast cancer cell growth and tumorigenesis. Our data have uncovered a critical regulator of estrogen/ERα-induced enhancer coding gene activation and breast cancer cell potency, providing a potential therapeutic target of ER-positive breast cancers.Entities:
Keywords: JmjC domain-containing protein; breast cancer; enhancer; enhancer RNA; estrogen receptor; mediator; protein arginine methyltransferase
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Year: 2018 PMID: 29628309 PMCID: PMC6258263 DOI: 10.1016/j.molcel.2018.03.006
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970