延伸系数
RNA聚合酶Ⅱ
聚四氟乙烯
抄写(语言学)
分子生物学
细胞生物学
转录因子II F
化学
核糖核酸
生物
RNA聚合酶
生物化学
基因表达
核糖体
基因
发起人
哲学
语言学
作者
Seychelle M. Vos,Lucas Farnung,Marc Boehning,Christoph Wigge,A. Linden,Henning Urlaub,Patrick Cramer
出处
期刊:Nature
[Springer Nature]
日期:2018-08-01
卷期号:560 (7720): 607-612
被引量:329
标识
DOI:10.1038/s41586-018-0440-4
摘要
Gene regulation involves activation of RNA polymerase II (Pol II) that is paused and bound by the protein complexes DRB sensitivity-inducing factor (DSIF) and negative elongation factor (NELF). Here we show that formation of an activated Pol II elongation complex in vitro requires the kinase function of the positive transcription elongation factor b (P-TEFb) and the elongation factors PAF1 complex (PAF) and SPT6. The cryo-EM structure of an activated elongation complex of Sus scrofa Pol II and Homo sapiens DSIF, PAF and SPT6 was determined at 3.1 Å resolution and compared to the structure of the paused elongation complex formed by Pol II, DSIF and NELF. PAF displaces NELF from the Pol II funnel for pause release. P-TEFb phosphorylates the Pol II linker to the C-terminal domain. SPT6 binds to the phosphorylated C-terminal-domain linker and opens the RNA clamp formed by DSIF. These results provide the molecular basis for Pol II pause release and elongation activation. The cryo-electron microscopy structure of an activated transcription elongation complex of RNA polymerase II bound to DRB sensitivity-inducing factor and the elongation factors PAF1 complex and SPT6 is reported at 3.1 Å resolution.
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