Tsai Chih-Cheng, Fondell Joseph D
Department of Physiology and Biophysics, UMDNJ, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
Vitam Horm. 2004;68:93-122. doi: 10.1016/S0083-6729(04)68003-4.
Nuclear receptors (NRs) compose one of the largest known families of eukaryotic transcription factors and, as such, serve as a paradigm for understanding the fundamental molecular mechanisms of eukaryotic transcriptional regulation. The packaging of eukaryotic genomic DNA into a higher ordered chromatin structure, which generally acts as a barrier to transcription by inhibiting transcription factor accessibility, has a major influence on the mechanisms by which NRs activate or repress gene expression. A major breakthrough in the field's understanding of these mechanisms comes from the recent identification of NR-associated coregulatory factors (i.e., coactivators and corepressors). Although several of these NR cofactors are involved in chromatin remodeling and facilitating the recruitment of the basal transcription machinery, the focus of this chapter is on NR coactivators and corepressors that act to covalently modify the amino-terminal tails of core histones. These modifications (acetylation, methylation, and phosphorylation) are thought to directly affect chromatin structure and?or serve as binding surfaces for other coregulatory proteins. This chapter presents the most current models for NR recruitment of histone-modifying enzymes and then summarizes their functional importance in NR-associated gene expression.
核受体(NRs)构成了已知最大的真核转录因子家族之一,因此,它们是理解真核转录调控基本分子机制的范例。真核基因组DNA包装成更高层次的染色质结构,通常通过抑制转录因子的可及性而对转录起到屏障作用,这对核受体激活或抑制基因表达的机制有重大影响。该领域对这些机制理解的一个重大突破来自于最近对与核受体相关的共调节因子(即共激活因子和共抑制因子)的鉴定。虽然其中一些核受体辅因子参与染色质重塑并促进基础转录机制的募集,但本章的重点是那些通过共价修饰核心组蛋白氨基末端尾巴而起作用的核受体共激活因子和共抑制因子。这些修饰(乙酰化、甲基化和磷酸化)被认为直接影响染色质结构和/或作为其他共调节蛋白的结合表面。本章介绍了核受体募集组蛋白修饰酶的最新模型,然后总结了它们在核受体相关基因表达中的功能重要性。