Evidence map›Paper›PMID 33616037›Full record

ArticleeLife2021

Dynamic interactions between the RNA chaperone Hfq, small regulatory RNAs, and mRNAs in live bacterial cells.

Seongjin Park, Karine Prévost, Emily M Heideman, Marie-Claude Carrier, Muhammad S Azam, Matthew A Reyer, Wei Liu, Eric Massé, Jingyi Fei

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Drug-resistantClinical microbiology reviews · 2025
    Pooled it
  2. Article
  3. TheInfection and immunity · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Competition for Hfq drives kinetic selection of mRNA targets byProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. TheFrontiers in cellular and infection microbiology · 2025
    Article
  15. Tevenvirinae phages encode a family of LSm-like fold proteins.Computational and structural biotechnology journal · 2025
    Article
  16. Achieving robust synthetic tolerance in industrialSynthetic and systems biotechnology · 2024
    Article
  17. Article
  18. Article
  19. Review
  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

9 authors at 2 institutions in 2 countries.

Seongjin Park *Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States.ORCID 0000-0002-4298-1770
Karine Prévost *RNA Group, Department of Biochemistry, University of Sherbrooke, Sherbrooke, Canada.
Emily M Heideman *Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States.
Marie-Claude Carrier *RNA Group, Department of Biochemistry, University of Sherbrooke, Sherbrooke, Canada.ORCID 0000-0002-3878-4141
Muhammad S AzamDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States.
Matthew A ReyerInstitute for Biophysical Dynamics, The University of Chicago, Chicago, United States.
Wei LiuDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States.
Eric MasséRNA Group, Department of Biochemistry, University of Sherbrooke, Sherbrooke, Canada.ORCID 0000-0002-5253-1415
Jingyi FeiDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States.ORCID 0000-0002-9775-3820
University of Chicago · USUniversité de Sherbrooke · CA

Funding

Molecular Determinants of Regulatory Hierarchy for Bacterial Small RNAsR01GM092830 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI VANDERPOOL, CARIN K · 2010 to 2020
$2.8M
Quantitative imaging of epitranscriptomic regulation mediated by RNA modificationDP2GM128185 · NIGMS · UNIVERSITY OF CHICAGO · PI FEI, JINGYI · 2017 to 2017
$2.4M
CIHR MOP69005NIGMS NIH HHS DP2 GM128185NIGMS NIH HHS R01 GM092830
6 · The paper itself

Abstract

RNA-binding proteins play myriad roles in regulating RNAs and RNA-mediated functions. In bacteria, the RNA chaperone Hfq is an important post-transcriptional gene regulator. Using live-cell super-resolution imaging, we can distinguish Hfq binding to different sizes of cellular RNAs. We demonstrate that under normal growth conditions, Hfq exhibits widespread mRNA-binding activity, with the distal face of Hfq contributing mostly to the mRNA binding in vivo. In addition, sRNAs can either co-occupy Hfq with the mRNA as a ternary complex, or displace the mRNA from Hfq in a binding face-dependent manner, suggesting mechanisms through which sRNAs rapidly access Hfq to induce sRNA-mediated gene regulation. Finally, our data suggest that binding of Hfq to certain mRNAs through its distal face can recruit RNase E to promote turnover of these mRNAs in a sRNA-independent manner, and such regulatory function of Hfq can be decoyed by sRNA competitors that bind strongly at the distal face.

Indexed as

Escherichia coliEscherichia coli ProteinsHost Factor 1 ProteinMolecular ChaperonesRNA, BacterialRNA, MessengerRNA Processing, Post-TranscriptionalRNA, Small UntranslatedEscherichia coli ProteinsHfq protein, E coliHost Factor 1 ProteinMolecular ChaperonesRNA, BacterialRNA, MessengerRNA, Small Untranslatedbiochemistrychemical biologyE. coligene regulationhfqinfectious diseasemicrobiologysingle-particle trackingsRNAsuper-resolution imaging

Identifiers

PMID33616037
PMCPMC7987339
OpenAlexW3132250380

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.