Evidence map›Paper›PMID 23720780›Full record

ArticleThe Journal of biological chemistry2013

Anthrax SET protein: a potential virulence determinant that epigenetically represses NF-κB activation in infected macrophages.

Shiraz Mujtaba, Benjamin Y Winer, Anbalagan Jaganathan, Jigneshkumar Patel, Miriam Sgobba, Raymond Schuch, Yogesh K Gupta, Shozeb Haider, Rong Wang, Vincent A Fischetti

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Histone modification cross talk between a host and pathogen.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Identification of potential nucleomodulins ofFrontiers in microbiology · 2024
    Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Commensal pneumococci go nuclear.Nature microbiology · 2021
    Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
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  20. 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

10 authors at 4 institutions in 2 countries.

Shiraz MujtabaDepartment of Structural and Chemical, Mount Sinai School of Medicine, New York, New York 10029, USA. shiraz.mujtaba@mssm.edu
Benjamin Y Winer
Anbalagan Jaganathan
Jigneshkumar Patel
Miriam Sgobba
Raymond Schuch
Yogesh K Gupta
Shozeb Haider
Rong Wang
Vincent A Fischetti
Institution of Structural Engineers · GBRockefeller University · USIcahn School of Medicine at Mount Sinai · USQueen's University Belfast · GB

Funding

Isolaton of new phage enzymes to kill B. anthracisR01AI057472 · NIAID · ROCKEFELLER UNIVERSITY · PI FISCHETTI, VINCENT A. · 2004 to 2014
$3.9M
Chemical Modulators for p53 Functions in Transcriptional RegulationR01CA143662 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MUJTABA, SYED SHIRAZ · 2010 to 2012
$926k
NCI NIH HHS 5R01CA143662-02NCI NIH HHS R01 CA143662NIAID NIH HHS 5R01AI057472NIAID NIH HHS R01 AI057472
6 · The paper itself

Abstract

Toxins play a major role in the pathogenesis of Bacillus anthracis by subverting the host defenses. However, besides toxins, B. anthracis expresses effector proteins, whose role in pathogenesis are yet to be investigated. Here we present that suppressor-of-variegation, enhancer-of-zeste, trithorax protein from B. anthracis (BaSET) methylates human histone H1, resulting in repression of NF-κB functions. Notably, BaSET is secreted and undergoes nuclear translocation to enhance H1 methylation in B. anthracis-infected macrophages. Compared with wild type Sterne, delayed growth kinetics and altered septum formation were observed in the BaSET knock-out (BaΔSET) bacilli. Uncontrolled BaSET expression during complementation of the BaSET gene in BaΔSET partially restored growth during stationary phase but resulted in substantially shorter bacilli throughout the growth cycle. Importantly, in contrast to Sterne, the BaΔSET B. anthracis is avirulent in a lethal murine bacteremia model of infection. Collectively, BaSET is required for repression of host transcription as well as proper B. anthracis growth, making it a potentially unique virulence determinant.

Indexed as

Bacillus anthracisEpigenesis, GeneticTranscription, GeneticAnimalsAnthraxBacterial ProteinsGene Expression Regulation, BacterialHeLa CellsHumansMacrophagesMiceNF-kappa BProtein MethyltransferasesVirulence FactorsBacterial ProteinsNF-kappa BProtein MethyltransferasesVirulence FactorsB. anthracisEpigeneticsGene RegulationHistone MethylationHost-pathogen InteractionsMicrobial PathogenesisNF-κBSeptation

Identifiers

PMID23720780
PMCPMC5395026
OpenAlexW1973229609

What OpenQuestion holds

Textmetadata
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.