Evidence map›Paper›PMID 35508531›Full record

ArticleNature communications2022

Diversity of bacterial small RNAs drives competitive strategies for a mutual chaperone.

Jorjethe Roca, Andrew Santiago-Frangos, Sarah A Woodson

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Exchange dynamics and kinetic control of gene regulation complexes.Nature reviews. Molecular cell biology · 2026
    Review
  2. Journal of molecular biology · 2026
    Article
  3. Review
  4. Competition for Hfq drives kinetic selection of mRNA targets byProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. What makes a small RNA work?Nucleic acids research · 2025
    Review
  6. Article
  7. Article
  8. Achieving robust synthetic tolerance in industrialSynthetic and systems biotechnology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Multiple RNA- and DNA-binding proteins exhibit direct transfer of polynucleotides with implications for target-site search.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. PRC2 direct transfer from G-quadruplex RNA to dsDNA has implications for RNA-binding chromatin modifiers.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. 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.

Jorjethe RocaT. C. Jenkins Department of Biophysics, Johns Hopkins University, 3400 N. Charles St., Baltimore, MD, 21218, USA.ORCID 0000-0002-9793-0110
Andrew Santiago-FrangosCMDB Program, Johns Hopkins University, 3400 N. Charles St., Baltimore, MD, 21218, USA.ORCID 0000-0001-9615-065X
Sarah A WoodsonT. C. Jenkins Department of Biophysics, Johns Hopkins University, 3400 N. Charles St., Baltimore, MD, 21218, USA. swoodson@jhu.edu.ORCID 0000-0003-0170-1987
Johns Hopkins University · US

Funding

Assembly Mechanisms of RNA-Protein Complexes for Genetic ControlR35GM136351 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI SARAH A. WOODSON · 2020 to 2026
$4.4M
NIGMS NIH HHS R35 GM136351
6 · The paper itself

Abstract

Hundreds of bacterial small RNAs (sRNAs) require the Hfq chaperone to regulate mRNA expression. Hfq is limiting, thus competition among sRNAs for binding to Hfq shapes the proteomes of individual cells. To understand how sRNAs compete for a common partner, we present a single-molecule fluorescence platform to simultaneously visualize binding and release of multiple sRNAs with Hfq. We show that RNA residents rarely dissociate on their own. Instead, clashes between residents and challengers on the same face of Hfq cause rapid exchange, whereas RNAs that recognize different surfaces may cohabit Hfq for several minutes before one RNA departs. The prevalence of these pathways depends on the structure of each RNA and how it interacts with Hfq. We propose that sRNA diversity creates many pairwise interactions with Hfq that allow for distinct biological outcomes: active exchange favors fast regulation whereas co-residence of dissimilar RNAs favors target co-recognition or target exclusion.

Indexed as

Escherichia coli ProteinsRNA, Small UntranslatedGene Expression Regulation, BacterialHost Factor 1 ProteinMolecular ChaperonesRNA, BacterialRNA, MessengerEscherichia coli ProteinsHost Factor 1 ProteinMolecular ChaperonesRNA, BacterialRNA, MessengerRNA, Small Untranslated

Identifiers

PMID35508531
PMCPMC9068810
OpenAlexW4225374302

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.