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蛋白激酶和蛋白酶体共同参与核视黄酸受体对转录的组合调控。

Protein kinases and the proteasome join in the combinatorial control of transcription by nuclear retinoic acid receptors.

作者信息

Bour Gaétan, Lalevée Sébastien, Rochette-Egly Cécile

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire, Department of Cell Biology and Signal Transduction, BP10142/Inserm, U596/CNRS, UMR7104, Illkirch, France.

出版信息

Trends Cell Biol. 2007 Jun;17(6):302-9. doi: 10.1016/j.tcb.2007.04.003. Epub 2007 Apr 30.

Abstract

Nuclear retinoic acid receptors (RARs) are transcriptional transregulators that control the expression of specific subsets of genes in a ligand-dependent manner. The basic mechanism for switching on gene transcription by agonist-liganded RARs involves their binding at specific response elements located in target genes. It also involves interactions with coregulatory protein complexes, the assembly of which is directed by the C-terminal ligand-binding domain of RARs. In addition to this scenario, several recent studies highlighted a fundamental role for the N-terminal domain in the transcriptional activity of RARs, following phosphorylation by the CDK7 kinase of the general transcription factor TFIIH and by p38MAPK. It has also emerged that the ubiquitin-proteasome system has a key role in RAR-mediated transcription. Here, we review new insights into how N-terminal domain and the proteasome pathway can influence the dynamics of RAR transcriptional activity.

摘要

核视黄酸受体(RARs)是转录反式调节因子,以配体依赖的方式控制特定基因子集的表达。激动剂配体化的RARs开启基因转录的基本机制包括它们与位于靶基因中的特定反应元件结合。这还涉及与共调节蛋白复合物的相互作用,其组装由RARs的C末端配体结合结构域指导。除了这种情况外,最近的几项研究强调了在一般转录因子TFIIH的CDK7激酶和p38MAPK磷酸化后,N末端结构域在RARs转录活性中的重要作用。还发现泛素-蛋白酶体系统在RAR介导的转录中起关键作用。在这里,我们综述了关于N末端结构域和蛋白酶体途径如何影响RAR转录活动动态的新见解。

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