Wu Susan C, Zhang Yi
Howard Hughes Medical Institute, Department of Biochemistry, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7295, USA.
Mol Endocrinol. 2009 Sep;23(9):1323-34. doi: 10.1210/me.2009-0131. Epub 2009 Apr 30.
Nuclear hormone receptors (NRs) are transcription factors responsible for mediating the biological effects of hormones during development, metabolism, and homeostasis. Induction of NR target genes is accomplished through the assembly of hormone-bound NR complexes at target promoters and coincides with changes in histone modifications that promote transcription. Some coactivators and corepressors of NR can enhance or inhibit NR function by covalently modifying histones. One such modification is methylation, which plays important roles in transcriptional regulation. Histone methylation is catalyzed by histone methyltransferases and reversed by histone demethylases. Recent studies have uncovered the importance of these enzymes in the regulation of NR target genes. In addition to histones, these enzymes have nonhistone substrates and can methylate and demethylate NRs and coregulatory proteins in order to modulate their function. This review discusses recent progress in our understanding of the role of methylation and demethylation of histones, NRs, and their coregulators in NR-mediated transcription.
核激素受体(NRs)是一类转录因子,负责在发育、代谢和体内平衡过程中介导激素的生物学效应。NR靶基因的诱导是通过在靶启动子处组装激素结合的NR复合物来实现的,并且与促进转录的组蛋白修饰变化相一致。NR的一些共激活因子和共抑制因子可以通过共价修饰组蛋白来增强或抑制NR功能。一种这样的修饰是甲基化,其在转录调控中起重要作用。组蛋白甲基化由组蛋白甲基转移酶催化,并由组蛋白去甲基化酶逆转。最近的研究揭示了这些酶在NR靶基因调控中的重要性。除了组蛋白外,这些酶还有非组蛋白底物,并且可以使NR和共调节蛋白甲基化和去甲基化,以调节它们的功能。本综述讨论了我们在理解组蛋白、NR及其共调节因子的甲基化和去甲基化在NR介导的转录中的作用方面的最新进展。