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Trigger loop dynamics mediate the balance between the transcriptional fidelity and speed of RNA polymerase II

机译:触发环动力学介导转录保真度和RNA聚合酶II速度之间的平衡

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摘要

During transcription, RNA polymerase II (RNAPII) must select the correct nucleotide, catalyze its addition to the growing RNA transcript, and move stepwise along the DNA until a gene is fully transcribed. In all kingdoms of life, transcription must be finely tuned to ensure an appropriate balance between fidelity and speed. Here, we used an optical-trapping assay with high spatiotemporal resolution to probe directly the motion of individual RNAPII molecules as they pass through each of the enzymatic steps of transcript elongation. We report direct evidence that the RNAPII trigger loop, an evolutionarily conserved protein subdomain, serves as a master regulator of transcription, affecting each of the three main phases of elongation, namely: substrate selection, translocation, and catalysis. Global fits to the force-velocity relationships of RNAPII and its trigger loop mutants support a Brownian ratchet model for elongation, where the incoming NTP is able to bind in either the pre- or posttranslocated state, and movement between these two states is governed by the trigger loop. Comparison of the kinetics of pausing by WT and mutant RNAPII under conditions that promote base misincorporation indicate that the trigger loop governs fidelity in substrate selection and mismatch recognition, and thereby controls aspects of both transcriptional accuracy and rate.
机译:在转录过程中,RNA聚合酶II(RNAPII)必须选择正确的核苷酸,催化其添加到正在生长的RNA转录物中,然后沿着DNA逐步移动,直到基因被完全转录。在生活的所有王国中,必须对转录进行微调,以确保保真度和速度之间的适当平衡。在这里,我们使用具有高时空分辨率的光阱测定法来直接探查单个RNAPII分子通过转录延长的每个酶促步骤时的运动。我们报告直接证据,RNAPII触发环,一个进化上保守的蛋白质亚结构域,充当转录的主要调控者,影响延伸的三个主要阶段,即底物选择,易位和催化。全局拟合符合RNAPII的力-速关系,其触发环突变体支持布朗棘轮模型的延伸,其中传入的NTP能够以易位或后易位状态结合,并且这两种状态之间的运动由触发循环。在促进碱基错误掺入的条件下,WT和突变RNAPII暂停的动力学比较表明,触发环控制底物选择和错配识别的保真度,从而控制转录准确性和速率。

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