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Multiple P-TEFbs cooperatively regulate the release of promoter-proximally paused RNA polymerase II

机译:多个P-TEFb协同调节启动子附近暂停的RNA聚合酶II的释放

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摘要

The association of DSIF and NELF with initiated RNA Polymerase II (Pol II) is the general mechanism for inducing promoter-proximal pausing of Pol II. However, it remains largely unclear how the paused Pol II is released in response to stimulation. Here, we show that the release of the paused Pol II is cooperatively regulated by multiple P-TEFbs which are recruited by bromodomain-containing protein Brd4 and super elongation complex (SEC) via different recruitment mechanisms. Upon stimulation, Brd4 recruits P-TEFb to Spt5/DSIF via a recruitment pathway consisting of Med1, Med23 and Tat-SF1, whereas SEC recruits P-TEFb to NELF-A and NELF-E via Paf1c and Med26, respectively. P-TEFb-mediated phosphorylation of Spt5, NELF-A and NELF-E results in the dissociation of NELF from Pol II, thereby transiting transcription from pausing to elongation. Additionally, we demonstrate that P-TEFb-mediated Ser2 phosphorylation of Pol II is dispensable for pause release. Therefore, our studies reveal a co-regulatory mechanism of Brd4 and SEC in modulating the transcriptional pause release by recruiting multiple P-TEFbs via a Mediator-and Paf1c-coordinated recruitment network.
机译:DSIF和NELF与起始的RNA聚合酶II(Pol II)的关联是诱导Pol II启动子临近暂停的一般机制。然而,仍然不清楚如何响应刺激释放暂停的Pol II。在这里,我们表明暂停的Pol II的释放是由多个P-TEFbs共同调控的,这些P-TEFbs由含溴结构域的蛋白B​​rd4和超伸长复合物(SEC)通过不同的募集机制募集。刺激后,Brd4通过Med1,Med23和Tat-SF1组成的募集途径将P-TEFb募集到Spt5 / DSIF,而SEC分别通过Paf1c和Med26将P-TEFb募集到NELF-A和NELF-E。 P-TEFb介导的Spt5,NELF-A和NELF-E磷酸化导致NELF与Pol II分离,从而使转录从暂停转变为延长。此外,我们证明了P-TEFb介导的Pol II的Ser2磷酸化对于暂停释放是必不可少的。因此,我们的研究揭示了Brd4和SEC在调节转录暂停释放中的共调节机制,该过程通过介体和Paf1c协调的募集网络募集多个P-TEFb。

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