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转录反应整合中的共激活因子和共抑制因子。

Co-activators and co-repressors in the integration of transcriptional responses.

作者信息

Torchia J, Glass C, Rosenfeld M G

机构信息

Howard Hughes Medical Institute, University of California San Diego 92093, USA.

出版信息

Curr Opin Cell Biol. 1998 Jun;10(3):373-83. doi: 10.1016/s0955-0674(98)80014-8.

Abstract

The nuclear hormone receptors are DNA binding transcription factors that are regulated by binding of ligands, switching them from an inactive or repressive state to gene-activating functions. Recent evidence supports the hypothesis that many nuclear receptors switch, in a ligand-dependent manner, between binding of a multicomponent co-repressor complex containing histone deacetyltransferase activity, and binding of a co-activator complex containing factors with histone acetyltransferase activity that are further regulated by diverse signal transduction pathways. The identification of these limiting co-repressor and co-activator complexes and their specific interaction motifs, in concert with solution of the structures of the receptor ligand-binding domain in apo (empty) and ligand bound forms, indicates a common molecular mechanism by which these factors activate and repress gene transcription.

摘要

核激素受体是DNA结合转录因子,通过配体结合进行调节,将它们从无活性或抑制状态转变为基因激活功能。最近的证据支持这样一种假说,即许多核受体以配体依赖的方式在含有组蛋白去乙酰化酶活性的多组分共抑制复合物的结合与含有具有组蛋白乙酰转移酶活性且受多种信号转导途径进一步调节的因子的共激活复合物的结合之间切换。这些限制性共抑制复合物和共激活复合物及其特定相互作用基序的鉴定,与无配体(空的)和结合配体形式的受体配体结合结构域的结构解析相结合,揭示了这些因子激活和抑制基因转录的共同分子机制。

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