Literature DB >> 1704199

A quantitative assessment for transcriptional pausing of DNA-dependent RNA polymerases in vitro.

G Theissen1, B Pardon, R Wagner.   

Abstract

A simple definition for pause strength (tau i) has been given, quantitatively describing transcriptional pausing of RNA polymerases. It permits derivation of practical assessments, based on single-round transcription reactions, which measure the average time a polymerase stops in vitro at certain sites during transcription elongation. We demonstrate that pause strengths can be determined with high accuracy when transcription elongation is started simultaneously from radioactively labeled and purified ternary complexes and transcripts are separated on sequencing gels. Our concept is exemplified by measuring pause strengths on supercoiled templates in the leader region of the Escherichia coli rrnB operon in the presence and the absence of the transcription factor NusA.

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Year:  1990        PMID: 1704199     DOI: 10.1016/0003-2697(90)90117-r

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  11 in total

1.  Pausing by bacterial RNA polymerase is mediated by mechanistically distinct classes of signals.

Authors:  I Artsimovitch; R Landick
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

Review 2.  Information processing by RNA polymerase: recognition of regulatory signals during RNA chain elongation.

Authors:  R A Mooney; I Artsimovitch; R Landick
Journal:  J Bacteriol       Date:  1998-07       Impact factor: 3.490

Review 3.  The Mechanisms of Substrate Selection, Catalysis, and Translocation by the Elongating RNA Polymerase.

Authors:  Georgiy A Belogurov; Irina Artsimovitch
Journal:  J Mol Biol       Date:  2019-05-31       Impact factor: 5.469

4.  A negative elongation factor for human RNA polymerase II inhibits the anti-arrest transcript-cleavage factor TFIIS.

Authors:  Murali Palangat; Dan B Renner; David H Price; Robert Landick
Journal:  Proc Natl Acad Sci U S A       Date:  2005-10-07       Impact factor: 11.205

5.  Folding of a large ribozyme during transcription and the effect of the elongation factor NusA.

Authors:  T Pan; I Artsimovitch; X W Fang; R Landick; T R Sosnick
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

6.  The NusA N-terminal domain is necessary and sufficient for enhancement of transcriptional pausing via interaction with the RNA exit channel of RNA polymerase.

Authors:  Kook Sun Ha; Innokenti Toulokhonov; Dmitry G Vassylyev; Robert Landick
Journal:  J Mol Biol       Date:  2010-06-25       Impact factor: 5.469

7.  Applied force provides insight into transcriptional pausing and its modulation by transcription factor NusA.

Authors:  Jing Zhou; Kook Sun Ha; Arthur La Porta; Robert Landick; Steven M Block
Journal:  Mol Cell       Date:  2011-11-18       Impact factor: 17.970

Review 8.  A Two-Way Street: Regulatory Interplay between RNA Polymerase and Nascent RNA Structure.

Authors:  Jinwei Zhang; Robert Landick
Journal:  Trends Biochem Sci       Date:  2016-01-25       Impact factor: 13.807

9.  In vitro transcription through nucleosomes by T7 RNA polymerase.

Authors:  N Kirov; I Tsaneva; E Einbinder; R Tsanev
Journal:  EMBO J       Date:  1992-05       Impact factor: 11.598

10.  Site-specific photolabile roadblocks for the study of transcription elongation in biologically complex systems.

Authors:  Jean-François Nadon; Vitaly Epshtein; Etienne Cameron; Mikhail R Samatov; Andrey S Vasenko; Evgeny Nudler; Daniel A Lafontaine
Journal:  Commun Biol       Date:  2022-05-12
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