Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
Genes Dev. 2012 Oct 1;26(19):2119-37. doi: 10.1101/gad.200303.112.
The C-terminal domain (CTD) of the RNA polymerase II largest subunit consists of multiple heptad repeats (consensus Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7), varying in number from 26 in yeast to 52 in vertebrates. The CTD functions to help couple transcription and processing of the nascent RNA and also plays roles in transcription elongation and termination. The CTD is subject to extensive post-translational modification, most notably phosphorylation, during the transcription cycle, which modulates its activities in the above processes. Therefore, understanding the nature of CTD modifications, including how they function and how they are regulated, is essential to understanding the mechanisms that control gene expression. While the significance of phosphorylation of Ser2 and Ser5 residues has been studied and appreciated for some time, several additional modifications have more recently been added to the CTD repertoire, and insight into their function has begun to emerge. Here, we review findings regarding modification and function of the CTD, highlighting the important role this unique domain plays in coordinating gene activity.
RNA 聚合酶 II 大亚基的 C 端结构域(CTD)由多个七肽重复序列(共识性 Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7)组成,其数量在酵母中变化范围为 26 个,在脊椎动物中变化范围为 52 个。CTD 有助于转录和新生 RNA 的加工偶联,也在转录延伸和终止中发挥作用。在转录周期中,CTD 会受到广泛的翻译后修饰,尤其是磷酸化修饰,这些修饰会调节其在上述过程中的活性。因此,了解 CTD 修饰的性质,包括它们的功能和调控方式,对于理解控制基因表达的机制至关重要。虽然 Ser2 和 Ser5 残基磷酸化的意义已经研究并得到了一定的认识,但最近又有几种额外的修饰被添加到 CTD 中,并且对它们的功能的认识也开始出现。在这里,我们回顾了 CTD 的修饰和功能的研究结果,强调了这个独特结构域在协调基因活性方面的重要作用。