Belakavadi M, Fondell J D
Department of Physiology and Biophysics, Robert Wood Johnson Medical School, UMDNJ, Piscataway, NJ 08854, USA.
Rev Physiol Biochem Pharmacol. 2006;156:23-43. doi: 10.1007/s10254-005-0002-0.
Mediator is an evolutionarily conserved multisubunit protein complex that plays a key role in regulating transcription by RNA polymerase II. The complex functions by serving as a molecular bridge between DNA-bound transcriptional activators and the basal transcription apparatus. In humans, Mediator was first characterized as a thyroid hormone receptor (TR)-associated protein (TRAP) complex that facilitates ligand-dependent transcriptional activation by TR. More recently, Mediator has been established as an essential coactivator for a broad range of nuclear hormone receptors (NRs) as well as several other types of gene-specific transcriptional activators. A single subunit of the complex, MED1/TRAP220, is required for direct ligand-dependent interactions with NRs. Mediator coactivates NR-regulated gene expression by facilitating the recruitment and activation of the RNA polymerase II-associated basal transcription apparatus. Importantly, Mediator acts in concert with other NR coactivators involved in chromatin remodeling to initiate transcription of NR target genes in a multistep manner. In this review, we summarize the functional role of Mediator in NR signaling pathways with an emphasis on the underlying molecular mechanisms by which the complex interacts with NRs and subsequently facilitates their action. We also focus on recent advances in our understanding of TRAP/Mediator's pathophysiological role in mammalian disease and development.
中介体是一种进化上保守的多亚基蛋白质复合物,在调节RNA聚合酶II介导的转录过程中起关键作用。该复合物通过作为DNA结合转录激活因子与基础转录装置之间的分子桥梁发挥作用。在人类中,中介体最初被表征为一种甲状腺激素受体(TR)相关蛋白(TRAP)复合物,可促进TR依赖配体的转录激活。最近,中介体已被确立为多种核激素受体(NRs)以及其他几种类型的基因特异性转录激活因子的必需共激活因子。该复合物的单个亚基MED1/TRAP220是与NRs直接进行配体依赖性相互作用所必需的。中介体通过促进与RNA聚合酶II相关的基础转录装置的募集和激活来共激活NR调节的基因表达。重要的是,中介体与参与染色质重塑的其他NR共激活因子协同作用,以多步骤方式启动NR靶基因的转录。在这篇综述中,我们总结了中介体在NR信号通路中的功能作用,重点关注该复合物与NRs相互作用并随后促进其作用的潜在分子机制。我们还关注了我们对TRAP/中介体在哺乳动物疾病和发育中的病理生理作用理解的最新进展。