| Literature DB >> 31103420 |
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.Entities:
Keywords: GreB; RNA polymerase structure; backtracking; cryo-EM; transcription; transcriptional arrest; transcriptional rescue
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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