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首页> 外文期刊>Molecular cell >Structural basis of transcription: mismatch-specific fidelity mechanisms and paused RNA polymerase II with frayed RNA.
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Structural basis of transcription: mismatch-specific fidelity mechanisms and paused RNA polymerase II with frayed RNA.

机译:转录的结构基础:错配特异性保真机制和暂停的RNA聚合酶II与磨损的RNA。

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摘要

We show that RNA polymerase (Pol) II prevents erroneous transcription in vitro with different strategies that depend on the type of DNARNA base mismatch. Certain mismatches are efficiently formed but impair RNA extension. Other mismatches allow for RNA extension but are inefficiently formed and efficiently proofread by RNA cleavage. X-ray analysis reveals that a TU mismatch impairs RNA extension by forming a wobble base pair at the Pol II active center that dissociates the catalytic metal ion and misaligns the RNA 3' end. The mismatch can also stabilize a paused state of Pol II with a frayed RNA 3' nucleotide. The frayed nucleotide binds in the Pol II pore either parallel or perpendicular to the DNA-RNA hybrid axis (fraying sites I and II, respectively) and overlaps the nucleoside triphosphate (NTP) site, explaining how it halts transcription during proofreading, before backtracking and RNA cleavage.
机译:我们显示RNA聚合酶(Pol)II防止体外转录错误,具体取决于DNARNA碱基错配的类型。某些错配可以有效形成,但会损害RNA延伸。其他错配允许RNA延伸,但是通过RNA切割不能有效形成并有效校对。 X射线分析表明,TU错配会通过在Pol II活性中心形成一个摆动碱基对来破坏RNA延伸,该碱基对会解离催化金属离子并使RNA 3'末端错位。错配还可以用磨损的RNA 3'核苷酸稳定Pol II的暂停状态。磨损的核苷酸在Pol II孔中平行或垂直于DNA-RNA杂合轴(分别位于断裂位点I和II)结合,并与三磷酸核苷(NTP)位点重叠,解释了它如何在校对过程中,回溯和终止前停止转录。 RNA切割。

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