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保守蛋白 Seb1 通过结合 RNA 聚合酶 II 和新生 RNA 来驱动转录终止。

The conserved protein Seb1 drives transcription termination by binding RNA polymerase II and nascent RNA.

机构信息

Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.

Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.

出版信息

Nat Commun. 2017 Apr 3;8:14861. doi: 10.1038/ncomms14861.

Abstract

Termination of RNA polymerase II (Pol II) transcription is an important step in the transcription cycle, which involves the dislodgement of polymerase from DNA, leading to release of a functional transcript. Recent studies have identified the key players required for this process and showed that a common feature of these proteins is a conserved domain that interacts with the phosphorylated C-terminus of Pol II (CTD-interacting domain, CID). However, the mechanism by which transcription termination is achieved is not understood. Using genome-wide methods, here we show that the fission yeast CID-protein Seb1 is essential for termination of protein-coding and non-coding genes through interaction with S2-phosphorylated Pol II and nascent RNA. Furthermore, we present the crystal structures of the Seb1 CTD- and RNA-binding modules. Unexpectedly, the latter reveals an intertwined two-domain arrangement of a canonical RRM and second domain. These results provide important insights into the mechanism underlying eukaryotic transcription termination.

摘要

RNA 聚合酶 II(Pol II)转录的终止是转录周期中的一个重要步骤,涉及从 DNA 上置换聚合酶,从而释放出有功能的转录本。最近的研究已经确定了这个过程所需的关键参与者,并表明这些蛋白质的一个共同特征是一个与 Pol II 磷酸化 C 末端(CTD 相互作用域,CID)相互作用的保守结构域。然而,转录终止的机制尚不清楚。在这里,我们使用全基因组方法表明,裂殖酵母 CID 蛋白 Seb1 通过与 S2 磷酸化的 Pol II 和新生 RNA 的相互作用,对于蛋白质编码和非编码基因的终止是必需的。此外,我们还展示了 Seb1 CTD 和 RNA 结合模块的晶体结构。出乎意料的是,后者揭示了一个典型的 RRM 和第二个结构域交织的双结构域排列。这些结果为真核转录终止的机制提供了重要的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f98c/5382271/5aa52b96c1dc/ncomms14861-f1.jpg

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