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Trigger loop of RNA polymerase is a positional, not acid–base, catalyst for both transcription and proofreading
by
Mishanina, Tatiana V.
, Palo, Michael Z.
, Mooney, Rachel A.
, Landick, Robert
, Nayak, Dhananjaya
in
Acids
/ Arginine
/ Bacteria
/ Biochemistry
/ Biological Sciences
/ Catalysis
/ Catalysts
/ Chemistry
/ DNA-directed RNA polymerase
/ E coli
/ Editing
/ Glutamine
/ Helices
/ Histidine
/ Hydrolysis
/ Nucleotides
/ Physical Sciences
/ PNAS Plus
/ Proofreading
/ Residues
/ Ribonucleic acid
/ RNA
/ Synthesis
/ Transcription
/ Transcription factors
2017
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Trigger loop of RNA polymerase is a positional, not acid–base, catalyst for both transcription and proofreading
by
Mishanina, Tatiana V.
, Palo, Michael Z.
, Mooney, Rachel A.
, Landick, Robert
, Nayak, Dhananjaya
in
Acids
/ Arginine
/ Bacteria
/ Biochemistry
/ Biological Sciences
/ Catalysis
/ Catalysts
/ Chemistry
/ DNA-directed RNA polymerase
/ E coli
/ Editing
/ Glutamine
/ Helices
/ Histidine
/ Hydrolysis
/ Nucleotides
/ Physical Sciences
/ PNAS Plus
/ Proofreading
/ Residues
/ Ribonucleic acid
/ RNA
/ Synthesis
/ Transcription
/ Transcription factors
2017
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Do you wish to request the book?
Trigger loop of RNA polymerase is a positional, not acid–base, catalyst for both transcription and proofreading
by
Mishanina, Tatiana V.
, Palo, Michael Z.
, Mooney, Rachel A.
, Landick, Robert
, Nayak, Dhananjaya
in
Acids
/ Arginine
/ Bacteria
/ Biochemistry
/ Biological Sciences
/ Catalysis
/ Catalysts
/ Chemistry
/ DNA-directed RNA polymerase
/ E coli
/ Editing
/ Glutamine
/ Helices
/ Histidine
/ Hydrolysis
/ Nucleotides
/ Physical Sciences
/ PNAS Plus
/ Proofreading
/ Residues
/ Ribonucleic acid
/ RNA
/ Synthesis
/ Transcription
/ Transcription factors
2017
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Trigger loop of RNA polymerase is a positional, not acid–base, catalyst for both transcription and proofreading
Journal Article
Trigger loop of RNA polymerase is a positional, not acid–base, catalyst for both transcription and proofreading
2017
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Overview
The active site of multisubunit RNA polymerases (RNAPs) is highly conserved from humans to bacteria. This single site catalyzes both nucleotide addition required for RNA transcript synthesis and excision of incorrect nucleotides after misincorporation as a proofreading mechanism. Phosphoryl transfer and proofreading hydrolysis are controlled in part by a dynamic RNAP component called the trigger loop (TL), which cycles between an unfolded loop and an α-helical hairpin [trigger helices (TH)] required for rapid nucleotide addition. The precise roles of the TL/TH in RNA synthesis and hydrolysis remain unclear. An invariant histidine residue has been proposed to function in the TH form as a general acid in RNA synthesis and as a general base in RNA hydrolysis. The effects of conservative, nonionizable substitutions of the TL histidine (or a neighboring TL arginine conserved in bacteria) have not yet been rigorously tested. Here, we report that glutamine substitutions of these residues, which preserve polar interactions but are incapable of acid–base chemistry, had little effect on either phosphoryl transfer or proofreading hydrolysis by Escherichia coli RNAP. The TL substitutions did, however, affect the backtracking of RNAP necessary for proofreading and potentially the reactivity of the backtracked nucleotide. We describe a unifying model for the function of the RNAP TL, which reconciles available data and our results for representative RNAPs. This model explains diverse effects of the TL basic residues on catalysis through their effects on positioning reactants for phosphoryl transfer and easing barriers to transcript backtracking, rather than as acid–base catalysts.
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