Department of Medical Protein Research, VIB, Ghent, Belgium.
Cytokine Growth Factor Rev. 2012 Dec;23(6):283-91. doi: 10.1016/j.cytogfr.2012.08.002. Epub 2012 Sep 16.
Besides the transcription-promoting role of histone acetyltransferases (HATs) and the transcription-delimiting function of histone deacetylases (HDACs) through histone acetylation and deacetylation respectively, HATs and HDACs also regulate the activity of several non-histone proteins. This includes signal transducers and activators of transcription (STATs), key proteins in cytokine signaling. Unlike Tyr phosphorylation/dephosphorylation, which mainly acts as an on/off switch of STAT activity, the control exerted by HATs and HDACs appears multifaceted and far more complex than initially imagined. Our review focuses on the latest trends and novel hypotheses to explain differential context-dependent STAT regulation by complex posttranslational modification patterns. We chart the knowledge on how STATs interact with HATs and HDACs, and additionally bring a transcriptional regulatory and gene-set specific role for HDACs in the picture. Indeed, a growing amount of evidence demonstrates, paradoxically, that not only HAT but also HDAC activity can be required for STAT-dependent transcription, in a STAT subtype- and cell type-dependent manner. Referring to recent reports, we review and discuss the various molecular mechanisms that have recently been proposed to account for this peculiar regulation, in an attempt to shed more light on the difficult yet important question on how STAT specificity is being generated.
除了组蛋白乙酰转移酶 (HATs) 通过组蛋白乙酰化和去乙酰化分别发挥转录促进作用和组蛋白去乙酰化酶 (HDACs) 发挥转录限制功能外,HATs 和 HDACs 还调节几种非组蛋白蛋白的活性。这包括信号转导子和转录激活子 (STATs),细胞因子信号转导中的关键蛋白。与主要作为 STAT 活性的开/关开关的 Tyr 磷酸化/去磷酸化不同,HATs 和 HDACs 发挥的控制作用似乎比最初想象的更为复杂和多方面。我们的综述重点介绍了最新趋势和新假设,以解释复杂的翻译后修饰模式对 STAT 调节的差异背景依赖性。我们描述了 STATs 与 HATs 和 HDACs 相互作用的知识,并进一步提出了 HDACs 在转录调控和基因集特异性方面在基因表达调控中的作用。事实上,越来越多的证据表明,不仅 HAT,而且 HDAC 的活性也可以依赖于 STAT,以依赖于 STAT 亚型和细胞类型的方式依赖于转录。参考最近的报告,我们综述和讨论了最近提出的各种分子机制,以解释这种特殊的调节,试图更清楚地阐明关于 STAT 特异性如何产生的困难但重要的问题。