Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination

Author:

Song Eunho1ORCID,Hwang Seungha2ORCID,Munasingha Palinda Ruvan3ORCID,Seo Yeon-Soo3,Kang Jin Young2ORCID,Kang Changwon34ORCID,Hohng Sungchul1ORCID

Affiliation:

1. Department of Physics and Astronomy, and Institute of Applied Physics, Seoul National University , Seoul  08826, Republic of Korea

2. Department of Chemistry, Korea Advanced Institute of Science and Technology , Daejeon  34141, Republic of Korea

3. Department of Biological Sciences, Korea Advanced Institute of Science and Technology , Daejeon  34141, Republic of Korea

4. KAIST Stem Cell Center, Korea Advanced Institute of Science and Technology , Daejeon  34141, Republic of Korea

Abstract

AbstractTranscriptional pause is essential for all types of termination. In this single-molecule study on bacterial Rho factor-dependent terminators, we confirm that the three Rho-dependent termination routes operate compatibly together in a single terminator, and discover that their termination efficiencies depend on the terminational pauses in unexpected ways. Evidently, the most abundant route is that Rho binds nascent RNA first and catches up with paused RNA polymerase (RNAP) and this catch-up Rho mediates simultaneous releases of transcript RNA and template DNA from RNAP. The fastest route is that the catch-up Rho effects RNA-only release and leads to 1D recycling of RNAP on DNA. The slowest route is that the RNAP-prebound stand-by Rho facilitates only the simultaneous rather than sequential releases. Among the three routes, only the stand-by Rho's termination efficiency positively correlates with pause duration, contrary to a long-standing speculation, invariably in the absence or presence of NusA/NusG factors, competitor RNAs or a crowding agent. Accordingly, the essential terminational pause does not need to be long for the catch-up Rho's terminations, and long pauses benefit only the stand-by Rho's terminations. Furthermore, the Rho-dependent termination of mgtA and ribB riboswitches is controlled mainly by modulation of the stand-by rather than catch-up termination.

Funder

National Research Foundation of Korea

High-Risk High-Return Project of KAIST

Korea Advanced Institute of Science and Technology

Publisher

Oxford University Press (OUP)

Subject

Genetics

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3