CTD公司
RNA聚合酶Ⅱ
生物
转录因子II F
抄写(语言学)
转录因子ⅡD
计算生物学
细胞生物学
一般转录因子
磷酸化
蛋白质亚单位
基因
核糖核酸
遗传学
基因表达
发起人
RNA聚合酶
地质学
语言学
哲学
海洋学
作者
Jing-Ping Hsin,James L. Manley
出处
期刊:Genes & Development
[Cold Spring Harbor Laboratory]
日期:2012-10-01
卷期号:26 (19): 2119-2137
被引量:665
标识
DOI:10.1101/gad.200303.112
摘要
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.
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