Literature DB >> 31103420

Structural Basis of Transcription: RNA Polymerase Backtracking and Its Reactivation.

Mo'men Abdelkareem1, Charlotte Saint-André1, Maria Takacs1, Gabor Papai1, Corinne Crucifix1, Xieyang Guo1, Julio Ortiz1, Albert Weixlbaumer2.   

Abstract

Regulatory sequences or erroneous incorporations during DNA transcription cause RNA polymerase backtracking and inactivation in all kingdoms of life. Reactivation requires RNA transcript cleavage. Essential transcription factors (GreA and GreB, or TFIIS) accelerate this reaction. We report four cryo-EM reconstructions of Escherichia coli RNA polymerase representing the entire reaction pathway: (1) a backtracked complex; a backtracked complex with GreB (2) before and (3) after RNA cleavage; and (4) a reactivated, substrate-bound complex with GreB before RNA extension. Compared with eukaryotes, the backtracked RNA adopts a different conformation. RNA polymerase conformational changes cause distinct GreB states: a fully engaged GreB before cleavage; a disengaged GreB after cleavage; and a dislodged, loosely bound GreB removed from the active site to allow RNA extension. These reconstructions provide insight into the catalytic mechanism and dynamics of RNA cleavage and extension and suggest how GreB targets backtracked complexes without interfering with canonical transcription.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  GreB; RNA polymerase structure; backtracking; cryo-EM; transcription; transcriptional arrest; transcriptional rescue

Mesh:

Substances:

Year:  2019        PMID: 31103420      PMCID: PMC7611809          DOI: 10.1016/j.molcel.2019.04.029

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  74 in total

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6.  The functional role of basic patch, a structural element of Escherichia coli transcript cleavage factors GreA and GreB.

Authors:  D Kulish; J Lee; I Lomakin; B Nowicka; A Das; S Darst; K Normet; S Borukhov
Journal:  J Biol Chem       Date:  2000-04-28       Impact factor: 5.157

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1.  Structural basis of Mfd-dependent transcription termination.

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6.  Obligate movements of an active site-linked surface domain control RNA polymerase elongation and pausing via a Phe pocket anchor.

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9.  Reliable identification of protein-protein interactions by crosslinking mass spectrometry.

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10.  In-cell architecture of an actively transcribing-translating expressome.

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