Evidence map›Paper›PMID 23043360›Full record

ArticleMolecular microbiology2012

The ribosome binding site of a mini-ORF protects a T3SS mRNA from degradation by RNase E.

Patricia B Lodato, Ping-Kun Hsieh, Joel G Belasco, James B Kaper

Abstract read
In one paragraph

Article in Molecular microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Minigene as a Novel Regulatory Element in Toxin-Antitoxin Systems.International journal of molecular sciences · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Initiation of mRNA decay in bacteria.Cellular and molecular life sciences : CMLS · 2014
    Review
  15. Article
  16. Article
  17. The social fabric of the RNA degradosome.Biochimica et biophysica acta
    Review
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

4 authors.

Patricia B LodatoDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Ping-Kun Hsieh
Joel G Belasco
James B Kaper

Funding

Prokaryotic RNA Metabolism - Resubmission - 1R01GM035769 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BELASCO, JOEL G · 1986 to 2021
$7.1M
Molecular Genetics of Enteropathogenic E. Coli AdhesionR37AI021657 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 2004 to 2013
$4.8M
NOVEL E. COLI 0157:H7 INTESTINAL COLONIZATION FACTORSR01DK058957 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 2000 to 2009
$3.1M
MOLECULAR GENETICS OF ENTEROPATHOGENIC E COLI ADHESIONR01AI021657 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 1989 to 2003
$1.4M
MOLECULAR GENETICS OF ENTEROPATHOGENIC E. COLI ADHESIONR22AI021657 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 1986 to 1991
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NIAID NIH HHS AI21657NIAID NIH HHS R01 AI021657NIAID NIH HHS R37 AI021657NIDDK NIH HHS DK58957NIDDK NIH HHS R01 DK058957NIGMS NIH HHS GM35769NIGMS NIH HHS R01 GM035769
6 · The paper itself

Abstract

Enterohaemorrhagic Escherichia coli harbours a pathogenicity island encoding a type 3 secretion system used to translocate effector proteins into the cytosol of intestinal epithelial cells and subvert their function. The structural proteins of the translocon are encoded in a major espADB mRNA processed from a precursor. The translocon mRNA should be highly susceptible to RNase E cleavage because of its AU-rich leader region and monophosphorylated 5'-terminus, yet it manages to avoid rapid degradation. Here, we report that the espADB leader region contains a strong Shine-Dalgarno element (SD2) and a translatable mini-ORF of six codons. Disruption of SD2 so as to weaken ribosome binding significantly reduces the concentration and stability of esp mRNA, whereas codon substitutions that impair translation of the mini-ORF have no such effect. These findings suggest that occupancy of SD2 by ribosomes, but not mini-ORF translation, helps to protect espADB mRNA from degradation, likely by hindering RNase E access to the AU-rich leader region.

Indexed as

AU Rich ElementsBacterial Outer Membrane ProteinsBacterial Secretion SystemsBinding SitesCodonEcthyma, ContagiousEndoribonucleasesEscherichia coliEscherichia coli ProteinsGene Expression Regulation, BacterialNucleic Acid ConformationProtein BiosynthesisRibosomesRNA, BacterialRNA, MessengerRNA StabilityBacterial Outer Membrane ProteinsBacterial Secretion SystemsCodonEaeB protein, E coliEndoribonucleasesEscherichia coli ProteinsEspA protein, E coliEspD protein, E coliribonuclease ERNA, BacterialRNA, Messenger

Identifiers

PMID23043360
PMCPMC3537511

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Registered trials

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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.