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6RIN

Cryo-EM structure of E. coli RNA polymerase backtracked elongation complex bound to GreB transcription factor

Summary for 6RIN
Entry DOI10.2210/pdb6rin/pdb
Related6RH3 6RI7 6RI9
EMDB information4892
DescriptorNon-template DNA, MAGNESIUM ION, Template DNA, ... (10 entities in total)
Functional Keywordse. coli rna polymerase, backtracking, greb, elongation complex, transcription
Biological sourceEscherichia coli K12
More
Total number of polymer chains9
Total formula weight436752.86
Authors
Abdelkareem, M.,Saint-Andre, C.,Takacs, M.,Papai, G.,Crucifix, C.,Guo, X.,Ortiz, J.,Weixlbaumer, A. (deposition date: 2019-04-24, release date: 2019-07-03, Last modification date: 2024-05-22)
Primary citationAbdelkareem, M.,Saint-Andre, C.,Takacs, M.,Papai, G.,Crucifix, C.,Guo, X.,Ortiz, J.,Weixlbaumer, A.
Structural Basis of Transcription: RNA Polymerase Backtracking and Its Reactivation.
Mol.Cell, 75:298-309.e4, 2019
Cited by
PubMed 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.
PubMed: 31103420
DOI: 10.1016/j.molcel.2019.04.029
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.7 Å)
Structure validation

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