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N-CoR-HDAC共抑制复合物:在核激素受体介导的转录调控中的作用

N-CoR-HDAC corepressor complexes: roles in transcriptional regulation by nuclear hormone receptors.

作者信息

Jones P L, Shi Y B

机构信息

Department of Cell and Structural Biology, University of Illinois at Urbana-Champaign, B107 CLSL, 601 S. Goodwin Ave, Urbana, IL 61801, USA.

出版信息

Curr Top Microbiol Immunol. 2003;274:237-68. doi: 10.1007/978-3-642-55747-7_9.

Abstract

Many nuclear hormone receptors (NHRs) actively repress the expression of their primary response genes through the recruitment of transcriptional corepressor complexes to regulated promoters. N-CoR and the highly related SMRT were originally isolated and characterized by their ability to interact exclusivelywith the unliganded forms of NHRs and confer transcriptional repression. Recently, both the N-CoR and SMRT corepressors have been found to exist in vivo in multiple, distinct macromolecular complexes. While these corepressor complexes differ in overall composition, a general theme is that they contain histone deacetylase enzymatic activity. Several of these complexes contain additional transcriptional corepressor proteins with functional ties to chromatin structure. Together, these data suggest that modulation of chromatin structure plays a central role in N-CoR mediated transcriptional repression from unliganded NHRs.

摘要

许多核激素受体(NHRs)通过招募转录共抑制复合物至调控的启动子区域,积极抑制其主要反应基因的表达。N-CoR和高度相关的SMRT最初是通过它们仅与未结合配体形式的NHRs相互作用并赋予转录抑制的能力而被分离和鉴定的。最近,人们发现N-CoR和SMRT共抑制因子在体内均以多种不同的大分子复合物形式存在。虽然这些共抑制复合物在整体组成上有所不同,但一个普遍的特点是它们都含有组蛋白脱乙酰酶的酶活性。其中一些复合物含有与染色质结构有功能联系的其他转录共抑制蛋白。这些数据共同表明,染色质结构的调节在未结合配体的NHRs介导的转录抑制中起着核心作用。

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