Evidence map›Paper›PMID 23340911›Full record

ReviewMetallomics : integrated biometal science2013

Iron-responsive bacterial small RNAs: variations on a theme.

Amanda G Oglesby-Sherrouse, Erin R Murphy

Open access · bronzeAbstract readReview
In one paragraph

Review in Metallomics : integrated biometal science, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 106 citations in OpenAlex.

  1. Article
  2. Article
  3. A small RNA fromVirulence · 2025
    Article
  4. Microbial metal physiology: ions to ecosystems.Nature reviews. Microbiology · 2025
    Review
  5. Linking Virulence and Iron Limitation Response inJournal of proteome research · 2025
    Article
  6. Review
  7. Microbiology spectrum · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. RyhB in Avian PathogenicInternational journal of molecular sciences · 2022
    Article
  18. Expanding the genetic toolkit helps dissect a global stress response in the early-branching speciesProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  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

2 authors at 1 institution in 1 country.

Amanda G Oglesby-SherrouseDepartment of Pharmaceutical Sciences, School of Pharmacy, Department of Microbiology and Immunology, School of Medicine, University of Maryland Baltimore, 20 Penn Street, Baltimore, MD, USA. aoglesby@rx.umaryland.edu
Erin R Murphy
In-Q-Tel · US

Funding

Mechanism of heme regulation of a P. aeruginosa non-coding RNAK22AI089776 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI OGLESBY, AMANDA GAIL · 2012 to 2013
$264k
NIAID NIH HHS 1K22AI089776-01A1NIAID NIH HHS K22 AI089776
6 · The paper itself

Abstract

For most living organisms, iron is both essential and potentially toxic, making the precise maintenance of iron homeostasis necessary for survival. To manage this paradox, bacteria regulate the acquisition, utilization, and storage of iron in response to its availability. The iron-dependent ferric uptake repressor (Fur) often mediates this iron-responsive regulation by both direct and indirect mechanisms. In 2002, Masse and Gottesman identified a novel target of Fur-mediated regulation in Escherichia coli: a gene encoding a small regulatory RNA (sRNA) termed RyhB. Under conditions of iron-limitation, RyhB is produced and functions to regulate the expression of several target genes encoding iron-utilizing enzymes, iron acquisition systems, and iron storage factors. This pivotal finding provided the missing link between environmental iron-limitation and previously observed decreases in certain iron-dependent metabolic pathways, a phenomenon now referred to as an "iron-sparing" response. The discovery of RyhB opened the door to the rapidly expanding field of bacterial iron-regulated sRNAs, which continue to be identified and described in numerous bacterial species. Most striking are findings that the impact of iron-responsive sRNA regulation often extends beyond iron homeostasis, particularly with regard to production of virulence-associated factors by pathogenic bacteria. This review discusses trends in the collective body of work on iron-regulated sRNAs, highlighting both the regulatory mechanisms they utilize to control target gene expression and the impact of this regulation on basic processes controlling bacterial physiology and virulence.

Indexed as

BacteriaIronModels, BiologicalRNA, AntisenseRNA, BacterialSequence Homology, Amino AcidIronRNA, AntisenseRNA, Bacterial

Identifiers

PMID23340911
PMCPMC3612141
OpenAlexW2044895510

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.