Evidence map›Paper›PMID 21399639›Full record

ArticleNature immunology2011

IKKβ phosphorylation regulates RPS3 nuclear translocation and NF-κB function during infection with Escherichia coli strain O157:H7.

Fengyi Wan, Amanda Weaver, Xiaofei Gao, Michael Bern, Philip R Hardwidge, Michael J Lenardo

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
8.6field-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

89 citing papers in PubMed, 140 citations in OpenAlex.

  1. Review
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  5. RPS3-Enriched Extracellular Vesicles Mediate Liver-Spinal Cord Inter-Organ Communication.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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29 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 1 country.

Fengyi WanLaboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Amanda Weaver
Xiaofei Gao
Michael Bern
Philip R Hardwidge
Michael J Lenardo
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USUniversity of Kansas Medical Center · US

Funding

XRAY CRYSTALLOGRAPHY CORE (JANUARY 1 - JUNE 30, 2005)P20RR016443 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI VINES, CHARLOTTE M · 2001 to 2010
$21.3M
Regulation of SIGNALLING PATHWAYS INVOLVING NUCLEAR FACTOR KAPPA BZIAAI000565 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LENARDO, MICHAEL J · 2009 to 2022
$5.2M
Novel Subunit of NF-kB Confers Gene Regulatory SpecificityR00CA137171 · NCI · JOHNS HOPKINS UNIVERSITY · PI WAN, FENGYI · 2011 to 2013
$710k
Disruption of NF-kB signaling by diarrheagenic Escherichia coliR56AI087686 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HARDWIDGE, PHILIP ROSS · 2010 to 2010
$370k
Host subversion by E. coli O157:H7 effector proteinsR03AI076227 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HARDWIDGE, PHILIP ROSS · 2009 to 2010
$149k
Intramural NIH HHSNCI NIH HHS R00 CA137171NCI NIH HHS R00CA137171NCRR NIH HHS P20 RR016443NIAID NIH HHS R03 AI076227NIAID NIH HHS R03AI076227NIAID NIH HHS R56 AI087686NIAID NIH HHS R56AI087686
6 · The paper itself

Abstract

NF-κB is a major gene regulator in immune responses, and ribosomal protein S3 (RPS3) is an NF-κB subunit that directs specific gene transcription. However, it is unknown how nuclear translocation of RPS3 is regulated. Here we report that phosphorylation of RPS3 Ser209 by the kinase IKKβ was crucial for nuclear localization of RPS3 in response to activating stimuli. Moreover, virulence protein NleH1 of the foodborne pathogen Escherichia coli strain O157:H7 specifically inhibited phosphorylation of RPS3 Ser209 and blocked RPS3 function, thereby promoting bacterial colonization and diarrhea but resulting in less mortality in a gnotobiotic piglet-infection model. Thus, the IKKβ-dependent modification of a specific amino acid in RPS3 promoted specific NF-κB functions that underlie the molecular pathogenetic mechanisms of E. coli O157:H7.

Indexed as

Active Transport, Cell NucleusAmino Acid SequenceAnimalsCell NucleusEscherichia coli InfectionsEscherichia coli O157Escherichia coli ProteinsHEK293 CellsHeLa CellsHost-Pathogen InteractionsHumansI-kappa B KinaseImmunoblottingJurkat CellsMolecular Sequence DataMutationEscherichia coli ProteinsI-kappa B KinaseNF-kappa BNleH protein, E coliRibosomal Proteinsribosomal protein S3Serine

Identifiers

PMID21399639
PMCPMC3062687
OpenAlexW2138135444

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.