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本文引用的文献

1
Phospho-MED1-enhanced UBE2C locus looping drives castration-resistant prostate cancer growth.磷酸化-MED1 增强的 UBE2C 基因座环化驱动去势抵抗性前列腺癌生长。
EMBO J. 2011 May 10;30(12):2405-19. doi: 10.1038/emboj.2011.154.
2
Med25 is required for RNA polymerase II recruitment to specific promoters, thus regulating xenobiotic and lipid metabolism in human liver.Med25 对于 RNA 聚合酶 II 招募到特定启动子是必需的,从而调节人肝脏中的外来物质和脂质代谢。
Mol Cell Biol. 2011 Feb;31(3):466-81. doi: 10.1128/MCB.00847-10. Epub 2010 Dec 6.
3
The metazoan Mediator co-activator complex as an integrative hub for transcriptional regulation.后生动物中介体共激活复合物作为转录调控的整合中心。
Nat Rev Genet. 2010 Nov;11(11):761-72. doi: 10.1038/nrg2901. Epub 2010 Oct 13.
4
SnapShot: NR coregulators.简讯:核共调节因子
Cell. 2010 Oct 1;143(1):172-172.e1. doi: 10.1016/j.cell.2010.09.032.
5
SnapShot: Nuclear receptors I.简要概述:核受体I。
Cell. 2010 Sep 3;142(5):822-822.e1. doi: 10.1016/j.cell.2010.08.026.
6
Mediator and cohesin connect gene expression and chromatin architecture.中介体和黏合蛋白连接基因表达和染色质结构。
Nature. 2010 Sep 23;467(7314):430-5. doi: 10.1038/nature09380. Epub 2010 Aug 18.
7
A muscle-specific knockout implicates nuclear receptor coactivator MED1 in the regulation of glucose and energy metabolism.肌肉特异性基因敲除表明核受体辅激活因子MED1参与葡萄糖和能量代谢的调控。
Proc Natl Acad Sci U S A. 2010 Jun 1;107(22):10196-201. doi: 10.1073/pnas.1005626107. Epub 2010 May 17.
8
Human ADA3 regulates RARalpha transcriptional activity through direct contact between LxxLL motifs and the receptor coactivator pocket.人 ADA3 通过 LxxLL 基序与受体辅激活子口袋之间的直接接触调节 RARalpha 转录活性。
Nucleic Acids Res. 2010 Sep;38(16):5291-303. doi: 10.1093/nar/gkq269. Epub 2010 Apr 22.
9
Key roles for MED1 LxxLL motifs in pubertal mammary gland development and luminal-cell differentiation.MED1 LxxLL 基序在青春期乳腺发育和腔细胞分化中的关键作用。
Proc Natl Acad Sci U S A. 2010 Apr 13;107(15):6765-70. doi: 10.1073/pnas.1001814107. Epub 2010 Mar 29.
10
MED14 tethers mediator to the N-terminal domain of peroxisome proliferator-activated receptor gamma and is required for full transcriptional activity and adipogenesis.MED14 将中介体连接到过氧化物酶体增殖物激活受体 γ 的 N 端结构域,是充分的转录活性和脂肪生成所必需的。
Mol Cell Biol. 2010 May;30(9):2155-69. doi: 10.1128/MCB.01238-09. Epub 2010 Mar 1.

中介依赖的核受体功能。

Mediator-dependent nuclear receptor function.

机构信息

Laboratory of Biochemistry and Molecular Biology, The Rockefeller University, 1230 York Ave., New York, NY 10065, USA.

出版信息

Semin Cell Dev Biol. 2011 Sep;22(7):749-58. doi: 10.1016/j.semcdb.2011.07.026. Epub 2011 Aug 10.

DOI:10.1016/j.semcdb.2011.07.026
PMID:21854863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3207035/
Abstract

As gene-specific transcription factors, nuclear receptors are broadly involved in many important biological processes. Their function on target genes requires the stepwise assembly of different coactivator complexes that facilitate chromatin remodeling and subsequent preinitiation complex (PIC) formation and function. Mediator has proved to be a crucial, and general, nuclear receptor-interacting coactivator, with demonstrated functions in transcription steps ranging from chromatin remodeling to subsequent PIC formation and function. Here we discuss our current understanding of (i) pathways involved in Mediator recruitment and function through nuclear receptor target gene enhancers and promoters, (ii) conditional requirements for the strong nuclear receptor-Mediator interactions mediated by NR AF2 domains and the MED1 LXXLL motifs, (iii) Mediator functions, through different nuclear receptor-interacting subunits, in different metabolic pathways, (iv) emerging functions of Mediator as a corepressor in addition to its major role as a coactivator and (v) mechanisms by which Mediator acts to transmit signals from enhancer-bound nuclear receptors to the general transcription machinery at core promoters to effect PIC formation and function. As a nuclear receptor coregulator with increasingly diverse functions, Mediator may thus modulate nuclear receptor signaling through several different mechanisms.

摘要

作为基因特异性转录因子,核受体广泛参与许多重要的生物学过程。它们在靶基因上的功能需要逐步组装不同的共激活因子复合物,这些复合物促进染色质重塑以及随后的起始前复合物(PIC)的形成和功能。共激活因子中介体已被证明是一种关键的、普遍的核受体相互作用的共激活因子,其在转录步骤中的功能从染色质重塑到随后的 PIC 形成和功能都得到了证实。在这里,我们讨论了我们目前对以下方面的理解:(i)通过核受体靶基因增强子和启动子参与中介体募集和功能的途径;(ii)通过核受体 AF2 结构域和 MED1 LXXLL 基序介导的强核受体-中介体相互作用的条件要求;(iii)通过不同的核受体相互作用亚基,中介体在不同代谢途径中的功能;(iv)中介体作为核心转录机器在核心启动子上从增强子结合的核受体传递信号的作用机制;(v)中介体作为除主要作为共激活因子之外的核心抑制剂的新兴功能。作为具有越来越多样化功能的核受体共调节剂,中介体可能通过几种不同的机制来调节核受体信号。