Evidence map›Paper›PMID 37116495›Full record

ArticleMolecular cell2023

Small RNAs and Hfq capture unfolded RNA target sites during transcription.

Margaret L Rodgers, Brett O'Brien, Sarah A Woodson

Open access · greenAbstract read
In one paragraph

Article in Molecular cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
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

26 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Exchange dynamics and kinetic control of gene regulation complexes.Nature reviews. Molecular cell biology · 2026
    Review
  3. Review
  4. Bacterial small regulatory RNAs.Nature reviews. Microbiology · 2026
    Review
  5. Design and discovery of 'tug-of-war' riboswitches.bioRxiv : the preprint server for biology · 2026
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Competition for Hfq drives kinetic selection of mRNA targets byProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Article
  15. Review
  16. Achieving robust synthetic tolerance in industrialSynthetic and systems biotechnology · 2024
    Article
  17. Article
  18. Co-transcriptional gene regulation in eukaryotes and prokaryotes.Nature reviews. Molecular cell biology · 2024
    Review
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Margaret L RodgersT.C. Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: margaret.rodgers@nih.gov.
Brett O'BrienChemical Biology Interface Program, Johns Hopkins University, Baltimore, MD 21218, USA.
Sarah A WoodsonT.C. Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: swoodson@jhu.edu.
Johns Hopkins University · US

Funding

Molecular mechanisms for co-transcriptional assembly of ribonucleoproteinsZIADK075175 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI RODGERS, MARGARET · 2023 to 2025
$7.2M
Assembly Mechanisms of RNA-Protein Complexes for Genetic ControlR35GM136351 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI SARAH A. WOODSON · 2020 to 2026
$4.4M
The Chemistry-Biology Interface Program at Johns Hopkins UniversityT32GM080189 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ROKITA, STEVEN E · 2008 to 2022
$3.5M
Molecular Mechanisms of Co-Transcriptional Ribonucleoprotein AssemblyK99GM140204 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI RODGERS, MARGARET LOUISE · 2021 to 2022
$180k
NIGMS NIH HHS K99 GM140204NIGMS NIH HHS R35 GM136351NIGMS NIH HHS T32 GM080189
6 · The paper itself

Abstract

Small ribonucleoproteins (sRNPs) target nascent precursor RNAs to guide folding, modification, and splicing during transcription. Yet, rapid co-transcriptional folding of the RNA can mask sRNP sites, impeding target recognition and regulation. To examine how sRNPs target nascent RNAs, we monitored binding of bacterial Hfq⋅DsrA sRNPs to rpoS transcripts using single-molecule co-localization co-transcriptional assembly (smCoCoA). We show that Hfq⋅DsrA recursively samples the mRNA before transcription of the target site to poise it for base pairing with DsrA. We adapted smCoCoA to precisely measure when the target site is synthesized and revealed that Hfq⋅DsrA often binds the mRNA during target site synthesis close to RNA polymerase (RNAP). We suggest that targeting transcripts near RNAP allows an sRNP to capture a site before the transcript folds, providing a kinetic advantage over post-transcriptional targeting. We propose that other sRNPs may also use RNAP-proximal targeting to hasten recognition and regulation.

Indexed as

Escherichia coli ProteinsRNA, Small UntranslatedBacterial ProteinsBase PairingEscherichia coliGene Expression Regulation, BacterialHost Factor 1 ProteinRNA, BacterialRNA, MessengerBacterial ProteinsEscherichia coli ProteinsHfq protein, E coliHost Factor 1 ProteinRNA, BacterialRNA, MessengerRNA, Small Untranslatedbacterial small RNAco-transcriptional RNA foldingHfqRNA chaperoneRNA polymerasesingle-molecule fluorescencesRNA regulation

Identifiers

PMID37116495
PMCPMC10176597
OpenAlexW4367325959

What OpenQuestion holds

Textmetadata
LicenceTDM
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.