Literature DB >> 29628309

JMJD6 Licenses ERα-Dependent Enhancer and Coding Gene Activation by Modulating the Recruitment of the CARM1/MED12 Co-activator Complex.

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.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  JmjC domain-containing protein; breast cancer; enhancer; enhancer RNA; estrogen receptor; mediator; protein arginine methyltransferase

Mesh:

Substances:

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


  94 in total

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Journal:  Mol Cell       Date:  2012-12-27       Impact factor: 17.970

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Authors:  Chin-Tong Ong; Victor G Corces
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Journal:  Cell Rep       Date:  2014-04-18       Impact factor: 9.423

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Authors:  Janice Kwok; Marie O'Shea; David A Hume; Andreas Lengeling
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Journal:  Nature       Date:  2012-09-06       Impact factor: 49.962

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  35 in total

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3.  In Silico Discovery of JMJD6 Inhibitors for Cancer Treatment.

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4.  The Ligand of Ate1 is intrinsically disordered and participates in nucleolar phase separation regulated by Jumonji Domain Containing 6.

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5.  The transcriptional co-activator NCOA6 promotes estrogen-induced GREB1 transcription by recruiting ERα and enhancing enhancer-promoter interactions.

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Journal:  J Biol Chem       Date:  2019-11-19       Impact factor: 5.157

6.  Prostaglandin A1 Decreases the Phosphorylation of Tau by Activating Protein Phosphatase 2A via a Michael Addition Mechanism at Cysteine 377.

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Review 7.  The emerging role of mediator complex subunit 12 in tumorigenesis and response to chemotherapeutics.

Authors:  Shengjie Zhang; Ruth O'Regan; Wei Xu
Journal:  Cancer       Date:  2019-12-23       Impact factor: 6.860

Review 8.  MED12-Related (Neuro)Developmental Disorders: A Question of Causality.

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Journal:  Genes (Basel)       Date:  2021-04-28       Impact factor: 4.096

9.  Gene Regulation Network Analysis on Human Prostate Orthografts Highlights a Potential Role for the JMJD6 Regulon in Clinical Prostate Cancer.

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10.  JMJD6 promotes self-renewal and regenerative capacity of hematopoietic stem cells.

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