The Mechanisms of Substrate Selection, Catalysis, and Translocation by the Elongating RNA Polymerase

被引:51
作者
Belogurov, Georgiy A. [1 ]
Artsimovitch, Irina [2 ,3 ]
机构
[1] Univ Turku, Dept Biochem, Turku, Finland
[2] Ohio State Univ, Dept Microbiol, 484 W 12th Ave, Columbus, OH 43210 USA
[3] Ohio State Univ, Ctr RNA Biol, Columbus, OH 43210 USA
基金
芬兰科学院; 美国国家卫生研究院;
关键词
TRANSCRIPT CLEAVAGE FACTORS; TRIGGER LOOP DYNAMICS; DNA-DEPENDENT RNA; NON-TEMPLATE DNA; ESCHERICHIA-COLI; STRUCTURAL BASIS; ACTIVE-SITE; SECONDARY CHANNEL; CRYSTAL-STRUCTURE; II ELONGATION;
D O I
10.1016/j.jmb.2019.05.042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multi-subunit DNA-dependent RNA polymerases synthesize all classes of cellular RNAs, ranging from short regulatory transcripts to gigantic messenger RNAs. RNA polymerase has to make each RNA product in just one try, even if it takes millions of successive nucleotide addition steps. During each step, RNA polymerase selects a correct substrate, adds it to a growing chain, and moves one nucleotide forward before repeating the cycle. However, RNA synthesis is anything but monotonous: RNA polymerase frequently pauses upon encountering mechanical, chemical and torsional barriers, sometimes stepping back and cleaving off nucleotides from the growing RNA chain. A picture in which these intermittent dynamics enable processive, accurate, and controllable RNA synthesis is emerging from complementary structural, biochemical, computational, and single-molecule studies. Here, we summarize our current understanding of the mechanism and regulation of the on-pathway transcription elongation. We review the details of substrate selection, catalysis, proofreading, and translocation, focusing on rate-limiting steps, structural elements that modulate them, and accessory proteins that appear to control RNA polymerase translocation. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3975 / 4006
页数:32
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