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本文引用的文献

1
Jmjd6, a JmjC Dioxygenase with Many Interaction Partners and Pleiotropic Functions.Jmjd6,一种具有多种相互作用伙伴和多效性功能的JmjC双加氧酶。
Front Genet. 2017 Mar 16;8:32. doi: 10.3389/fgene.2017.00032. eCollection 2017.
2
JMJD6 and U2AF65 co-regulate alternative splicing in both JMJD6 enzymatic activity dependent and independent manner.JMJD6和U2AF65以依赖和不依赖JMJD6酶活性的方式共同调节可变剪接。
Nucleic Acids Res. 2017 Apr 7;45(6):3503-3518. doi: 10.1093/nar/gkw1144.
3
JARID1/KDM5 demethylases as cancer targets?JARID1/KDM5去甲基化酶可作为癌症治疗靶点吗?
Expert Opin Ther Targets. 2017 Jan;21(1):5-7. doi: 10.1080/14728222.2017.1263616. Epub 2016 Nov 28.
4
Lysine demethylase KDM3A regulates breast cancer cell invasion and apoptosis by targeting histone and the non-histone protein p53.赖氨酸去甲基化酶KDM3A通过靶向组蛋白和非组蛋白p53调节乳腺癌细胞的侵袭和凋亡。
Oncogene. 2017 Jan 5;36(1):47-59. doi: 10.1038/onc.2016.174. Epub 2016 Jun 6.
5
The epigenetic modifier JMJD6 is amplified in mammary tumors and cooperates with c-Myc to enhance cellular transformation, tumor progression, and metastasis.表观遗传修饰因子JMJD6在乳腺肿瘤中扩增,并与c-Myc协同作用,增强细胞转化、肿瘤进展和转移。
Clin Epigenetics. 2016 Apr 14;8:38. doi: 10.1186/s13148-016-0205-6. eCollection 2016.
6
Activation of P-TEFb by Androgen Receptor-Regulated Enhancer RNAs in Castration-Resistant Prostate Cancer.去势抵抗性前列腺癌中雄激素受体调节的增强子RNA对P-TEFb的激活作用
Cell Rep. 2016 Apr 19;15(3):599-610. doi: 10.1016/j.celrep.2016.03.038. Epub 2016 Apr 7.
7
BET Bromodomain Inhibition Releases the Mediator Complex from Select cis-Regulatory Elements.BET 溴结构域抑制作用可使中介体复合物从特定顺式调控元件上释放出来。
Cell Rep. 2016 Apr 19;15(3):519-530. doi: 10.1016/j.celrep.2016.03.054. Epub 2016 Apr 7.
8
MED12 methylation by CARM1 sensitizes human breast cancer cells to chemotherapy drugs.CARM1介导的MED12甲基化使人类乳腺癌细胞对化疗药物敏感。
Sci Adv. 2015 Oct 9;1(9):e1500463. doi: 10.1126/sciadv.1500463. eCollection 2015 Oct.
9
Dynamic Arginine Methylation of Tumor Necrosis Factor (TNF) Receptor-associated Factor 6 Regulates Toll-like Receptor Signaling.肿瘤坏死因子(TNF)受体相关因子6的动态精氨酸甲基化调控Toll样受体信号传导。
J Biol Chem. 2015 Sep 4;290(36):22236-49. doi: 10.1074/jbc.M115.653543. Epub 2015 Jul 28.
10
Loading of PAX3 to Mitotic Chromosomes Is Mediated by Arginine Methylation and Associated with Waardenburg Syndrome.PAX3向有丝分裂染色体的加载由精氨酸甲基化介导,并与瓦登伯格综合征相关。
J Biol Chem. 2015 Aug 14;290(33):20556-64. doi: 10.1074/jbc.M114.607713. Epub 2015 Jul 6.

JMJD6 通过调节 CARM1/MED12 共激活复合物的募集来激活 ERα 依赖性增强子和编码基因。

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

机构信息

School of Pharmaceutical Sciences, Fujian Provincial Key Laboratory of Innovative Drug Target Research, Xiamen University, Xiang'an South Road, Xiamen, Fujian 361102, China.

Howard Hughes Medical Institute, Department of Medicine, School of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.

出版信息

Mol Cell. 2018 Apr 19;70(2):340-357.e8. doi: 10.1016/j.molcel.2018.03.006. Epub 2018 Apr 5.

DOI:10.1016/j.molcel.2018.03.006
PMID:29628309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6258263/
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.

摘要

虽然增强子在基因转录调控中的作用已得到充分证实,但 JmjC 结构域蛋白在介导增强子激活中的作用仍知之甚少。在这里,我们报告说,JmjC 结构域蛋白 6(JMJD6)被招募到雌激素受体 alpha(ERα)结合的活性增强子上,是招募 RNA 聚合酶 II 和增强子 RNA 产生所必需的,从而导致同源雌激素靶基因的转录暂停释放。发现 JMJD6 与中介复合物中的 MED12 相互作用,以调节其募集。出乎意料的是,JMJD6 对于 MED12 与 CARM1 的相互作用是必需的,CARM1 在多个精氨酸位点甲基化 MED12,并调节其染色质结合。与它在转录激活中的作用一致,JMJD6 是雌激素/ERα 诱导的乳腺癌细胞生长和肿瘤发生所必需的。我们的数据揭示了雌激素/ERα 诱导的增强子编码基因激活和乳腺癌细胞效力的关键调节因子,为 ER 阳性乳腺癌提供了一个潜在的治疗靶点。