Antitermination protein P7 of bacteriophage Xp10 distinguishes different types of transcriptional pausing by bacterial RNA polymerase

被引:1
|
作者
Prostova, Maria [1 ]
Kulbachinskiy, Andrey [1 ]
Esyunina, Daria [1 ]
机构
[1] Russian Acad Sci, Inst Mol Genet, Kurchatov Sq 2, Moscow 123182, Russia
基金
俄罗斯科学基金会; 俄罗斯基础研究基金会;
关键词
RNA polymerase; Transcriptional pausing; NusA; Transcription antitermination; Bacteriophage; N-TERMINAL DOMAIN; ELONGATION COMPLEXES; SIGMA(70) SUBUNIT; STRUCTURAL BASIS; EXIT CHANNEL; NUSA; DNA; SPECIFICITY; INITIATION; MECHANISM;
D O I
10.1016/j.biochi.2019.12.011
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
Bacteriophage-encoded transcription antiterminators play essential roles in the regulation of gene expression during infection. Here, we characterize the effects of the antiterminator protein P7 of bacteriophage Xp10 on transcriptional pausing by Xanthomonas oryzae RNA polymerase (RNAP) at different types of pause-inducing signals. When acting alone, P7 inhibits only hairpin-stabilized pauses, likely by preventing hairpin formation. In the presence of NusA, P7 also suppresses backtracking-stabilized pauses and the his elemental pause, but not the consensus elemental pause, suggesting that these pause signals may be mechanistically different. Thus, P7 and other bacteriophage proteins that bind near the RNA exit channel of RNAP have evolved to regulate transcription by suppressing RNAP pausing at a subset of regulatory signals, and to co-opt NusA in doing so. (C) 2020 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.
引用
收藏
页码:57 / 64
页数:8
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