Evidence map›Paper›PMID 24706744›Full record

ArticleJournal of bacteriology2014

FlgN is required for flagellum-based motility by Bacillus subtilis.

Lynne S Cairns, Victoria L Marlow, Taryn B Kiley, Christopher Birchall, Adam Ostrowski, Phillip D Aldridge, Nicola R Stanley-Wall

Open access · hybridAbstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Motility inMicroorganisms · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Quantification of Motility inFrontiers in microbiology · 2022
    Article
  8. Review
  9. Completed Genomic Sequence ofG3 (Bethesda, Md.) · 2020
    Article
  10. Genomic sequencing-based mutational enrichment analysis identifies motility genes in a genetically intractable gut microbe.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  11. 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

7 authors at 2 institutions in 1 country.

Lynne S CairnsDivision of Molecular Microbiology, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
Victoria L MarlowDivision of Molecular Microbiology, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
Taryn B KileyDivision of Molecular Microbiology, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
Christopher BirchallCentre for Bacterial Cell Biology, Newcastle University, Newcastle upon Tyne, United Kingdom.
Adam OstrowskiDivision of Molecular Microbiology, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
Phillip D AldridgeCentre for Bacterial Cell Biology, Newcastle University, Newcastle upon Tyne, United Kingdom.
Nicola R Stanley-WallDivision of Molecular Microbiology, College of Life Sciences, University of Dundee, Dundee, United Kingdom n.r.stanleywall@dundee.ac.uk.ORCID http://orcid.org/0000-0002-5936-9721
University of Dundee · GBNewcastle University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D526161/1Biotechnology and Biological Sciences Research Council BB/H002340/1Biotechnology and Biological Sciences Research Council BB/I006915/1Wellcome Trust 083524/Z/07/ZWellcome Trust 093714/Z/10/Z
6 · The paper itself

Abstract

The assembly of the bacterial flagellum is exquisitely controlled. Flagellar biosynthesis is underpinned by a specialized type III secretion system that allows export of proteins from the cytoplasm to the nascent structure. Bacillus subtilis regulates flagellar assembly using both conserved and species-specific mechanisms. Here, we show that YvyG is essential for flagellar filament assembly. We define YvyG as an orthologue of the Salmonella enterica serovar Typhimurium type III secretion system chaperone, FlgN, which is required for the export of the hook-filament junction proteins, FlgK and FlgL. Deletion of flgN (yvyG) results in a nonmotile phenotype that is attributable to a decrease in hag translation and a complete lack of filament polymerization. Analyses indicate that a flgK-flgL double mutant strain phenocopies deletion of flgN and that overexpression of flgK-flgL cannot complement the motility defect of a ΔflgN strain. Furthermore, in contrast to previous work suggesting that phosphorylation of FlgN alters its subcellular localization, we show that mutation of the identified tyrosine and arginine FlgN phosphorylation sites has no effect on motility. These data emphasize that flagellar biosynthesis is differentially regulated in B. subtilis from classically studied Gram-negative flagellar systems and questions the biological relevance of some posttranslational modifications identified by global proteomic approaches.

Indexed as

Amino Acid SequenceBacillus subtilisBacterial ProteinsFlagellaGene Expression Regulation, BacterialMolecular Sequence DataMovementMutationBacterial ProteinsFlgN protein, Bacteria

Identifiers

PMID24706744
PMCPMC4054197
OpenAlexW2120133080

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.