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RNA 聚合酶 II 通过三步机制逃脱启动子。

Three-step mechanism of promoter escape by RNA polymerase II.

机构信息

Max Planck Institute for Multidisciplinary Sciences, Department of Molecular Biology, Am Fassberg 11, 37077 Göttingen, Germany.

Max Planck Institute for Multidisciplinary Sciences, Department of Molecular Biology, Am Fassberg 11, 37077 Göttingen, Germany.

出版信息

Mol Cell. 2024 May 2;84(9):1699-1710.e6. doi: 10.1016/j.molcel.2024.03.016. Epub 2024 Apr 10.

Abstract

The transition from transcription initiation to elongation is highly regulated in human cells but remains incompletely understood at the structural level. In particular, it is unclear how interactions between RNA polymerase II (RNA Pol II) and initiation factors are broken to enable promoter escape. Here, we reconstitute RNA Pol II promoter escape in vitro and determine high-resolution structures of initially transcribing complexes containing 8-, 10-, and 12-nt ordered RNAs and two elongation complexes containing 14-nt RNAs. We suggest that promoter escape occurs in three major steps. First, the growing RNA displaces the B-reader element of the initiation factor TFIIB without evicting TFIIB. Second, the rewinding of the transcription bubble coincides with the eviction of TFIIA, TFIIB, and TBP. Third, the binding of DSIF and NELF facilitates TFIIE and TFIIH dissociation, establishing the paused elongation complex. This three-step model for promoter escape fills a gap in our understanding of the initiation-elongation transition of RNA Pol II transcription.

摘要

人类细胞中转录起始到延伸的转变受到高度调控,但在结构水平上仍不完全清楚。特别是,尚不清楚 RNA 聚合酶 II (RNA Pol II) 和起始因子之间的相互作用如何被打破以实现启动子逃逸。在这里,我们在体外重新构建了 RNA Pol II 启动子逃逸,并确定了包含 8-、10-和 12-nt 有序 RNA 的最初转录复合物以及包含 14-nt RNA 的两个延伸复合物的高分辨率结构。我们认为启动子逃逸分三个主要步骤发生。首先,延伸中的 RNA 取代起始因子 TFIIB 的 B-reader 元件,而不驱逐 TFIIB。其次,转录泡的回卷与 TFIIA、TFIIB 和 TBP 的驱逐同时发生。第三,DSIF 和 NELF 的结合促进了 TFIIE 和 TFIIH 的解离,建立了暂停延伸复合物。这种启动子逃逸的三步模型填补了我们对 RNA Pol II 转录起始延伸转变理解的空白。

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