Head-on and co-directional RNA polymerase collisions orchestrate bidirectional transcription termination

被引:11
作者
Wang, Ling [1 ,2 ]
Watters, John W. [1 ]
Ju, Xiangwu [1 ]
Lu, Genzhe [1 ]
Liu, Shixin [1 ]
机构
[1] Rockefeller Univ, Lab Nanoscale Biophys & Biochem, New York, NY 10065 USA
[2] Southern Univ Sci & Technol, Sch Life Sci, Dept Biol, Shenzhen, Peoples R China
基金
美国国家卫生研究院;
关键词
SINGLE-MOLECULE; CLEAVAGE FACTORS; ELONGATION; PROTEIN; INTERFERENCE; COOPERATION; MECHANISMS; DYNAMICS; FORCE; GREB;
D O I
10.1016/j.molcel.2023.02.017
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
Genomic DNA is a crowded track where motor proteins frequently collide. It remains underexplored whether these collisions carry physiological function. In this work, we develop a single-molecule assay to visualize the trafficking of individual E. coli RNA polymerases (RNAPs) on DNA. Based on transcriptomic data, we hypoth-esize that RNAP collisions drive bidirectional transcription termination of convergent gene pairs. Single -molecule results show that the head-on collision between two converging RNAPs is necessary to prevent transcriptional readthrough but insufficient to release the RNAPs from the DNA. Remarkably, co-directional collision of a trailing RNAP into the head-on collided complex dramatically increases the termination effi-ciency. Furthermore, stem-loop structures formed in the nascent RNA are required for collisions to occur at well-defined positions between convergent genes. These findings suggest that physical collisions be-tween RNAPs furnish a mechanism for transcription termination and that programmed genomic conflicts can be exploited to co-regulate the expression of multiple genes.
引用
收藏
页码:1153 / +
页数:17
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