Evidence map›Paper›PMID 23769674›Full record

ArticleMolecular cell2013

Cys-pair reporters detect a constrained trigger loop in a paused RNA polymerase.

Dhananjaya Nayak, Michael Voss, Tricia Windgassen, Rachel Anne Mooney, Robert Landick

Abstract read
In one paragraph

Article in Molecular cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Higher-order epistasis within Pol II trigger loop haplotypes.bioRxiv : the preprint server for biology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Obligate movements of an active site-linked surface domain control RNA polymerase elongation and pausing via a Phe pocket anchor.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Closing and opening of the RNA polymerase trigger loop.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. Review
  11. Mechanisms of Transcriptional Pausing in Bacteria.Journal of molecular biology · 2019
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Transcriptional Responses to ppGpp and DksA.Annual review of microbiology · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Trigger loop of RNA polymerase is a positional, not acid-base, catalyst for both transcription and proofreading.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
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

5 authors.

Dhananjaya NayakDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Michael Voss
Tricia Windgassen
Rachel Anne Mooney
Robert Landick

Funding

STRUCTURE/FUNCTION OF TRANSCRIPTION COMPLEX RNA HAIRPINSR01GM038660 · NIGMS · WASHINGTON UNIVERSITY · PI Robert Landick · 1992 to 2026
$12.2M
Structure/Function of Transcription Complex RNA HairpinsR37GM038660 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI LANDICK, ROBERT · 2001 to 2010
$5.5M
STRUCTURE/FUNCTION OF TRANSCRIPTION COMPLEX RNA HAIRPINSR29GM038660 · NIGMS · WASHINGTON UNIVERSITY · PI LANDICK, ROBERT · 1987 to 1991
–
NIGMS NIH HHS GM38660NIGMS NIH HHS R01 GM038660NIGMS NIH HHS R37 GM038660
6 · The paper itself

Abstract

Transcriptional pausing, which regulates transcript elongation in both prokaryotes and eukaryotes, is thought to involve formation of alternative RNA polymerase conformations in which nucleotide addition is inhibited in part by restriction of trigger loop (TL) folding. The polymorphous TL must convert from a random coil to a helical hairpin that contacts the nucleotide triphosphate (NTP) substrate to allow rapid nucleotide addition. Understanding the distribution of TL conformations in different enzyme states is made difficult by the TL's small size and sensitive energetics. Here, we report a Cys-pair reporter strategy to elucidate the relative occupancies of different TL conformations in E. coli RNA polymerase based on the ability of Cys residues engineered into the TL and surrounding regions to form disulfide bonds. Our results indicate that a paused complex stabilized by a nascent RNA hairpin favors nonproductive TL conformations that persist after NTP binding but can be reversed by the elongation factor RfaH.

Indexed as

Adenosine TriphosphateAmino Acid MotifsBase SequenceCystamineCystineDNA-Directed RNA PolymerasesEscherichia coliEscherichia coli ProteinsGuanosine TriphosphateInverted Repeat SequencesModels, MolecularOxidation-ReductionPeptide Elongation FactorsProtein BindingProtein ConformationRNAAdenosine TriphosphateCystamineCystineDNA-Directed RNA PolymerasesEscherichia coli ProteinsGreB protein, E coliGuanosine TriphosphatePeptide Elongation FactorsRfaH protein, E coliRNATrans-ActivatorsTranscriptional Elongation Factors

Identifiers

PMID23769674
PMCPMC4037917

What OpenQuestion holds

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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.