Evidence map›Paper›PMID 25552559›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Trigger loop folding determines transcription rate of Escherichia coli's RNA polymerase.

Yara X Mejia, Evgeny Nudler, Carlos Bustamante

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. RNA polymerase inhibitors reveal active-site motions essential for the nucleotide addition cycle.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
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  4. Nanopore tweezers show fractional-nucleotide translocation in sequence-dependent pausing by RNA polymerase.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Article
  7. Closing and opening of the RNA polymerase trigger loop.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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  10. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yara X MejiaJason L. Choy Laboratory of Single-Molecule Biophysics, the California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, CA 94720;
Evgeny NudlerDepartment of Biochemistry and Molecular Pharmacology and Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016;
Carlos BustamanteJason L. Choy Laboratory of Single-Molecule Biophysics, the California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, CA 94720; Department of Molecular and Cell Biology, Department of Physics, Department of Chemistry, Biophysics Graduate Group and Howard Hughes Medical Institute, University of California, Berkeley, CA 94720; and Kavli Energy Nanosciences Institute at Berkeley, Berkeley, CA 94720 carlos@alice.berkeley.edu.

Funding

THE PHYSICAL CHEMISTRY OF NUCLEIC ACIDSR01GM032543 · NIGMS · UNIVERSITY OF OREGON · PI CARLOS Jose BUSTAMANTE · 1985 to 2026
$6.4M
Role of RNA polymerase in DNA stability and repairR01GM107329 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NUDLER, EVGENY A · 2014 to 2017
$1.7M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM032543NIGMS NIH HHS R01-GM0325543NIGMS NIH HHS R01 GM107329NIGMS NIH HHS R01GM107329
6 · The paper itself

Abstract

Two components of the RNA polymerase (RNAP) catalytic center, the bridge helix and the trigger loop (TL), have been linked with changes in elongation rate and pausing. Here, single molecule experiments with the WT and two TL-tip mutants of the Escherichia coli enzyme reveal that tip mutations modulate RNAP's pause-free velocity, identifying TL conformational changes as one of two rate-determining steps in elongation. Consistent with this observation, we find a direct correlation between helix propensity of the modified amino acid and pause-free velocity. Moreover, nucleotide analogs affect transcription rate, suggesting that their binding energy also influences TL folding. A kinetic model in which elongation occurs in two steps, TL folding on nucleoside triphosphate (NTP) binding followed by NTP incorporation/pyrophosphate release, quantitatively accounts for these results. The TL plays no role in pause recovery remaining unfolded during a pause. This model suggests a finely tuned mechanism that balances transcription speed and fidelity.

Indexed as

Protein FoldingTranscription, GeneticDNA-Directed RNA PolymerasesEscherichia coliKineticsModels, MolecularDNA-Directed RNA Polymerasesoptical tweezersRNA polymerasesingle moleculetranscriptiontrigger loop

Identifiers

PMID25552559
PMCPMC4311812

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.