Evidence map›Paper›PMID 25138908›Full record

ArticleMolecular microbiology2014

MG428 is a novel positive regulator of recombination that triggers mgpB and mgpC gene variation in Mycoplasma genitalium.

Raul Burgos, Patricia A Totten

Open access · bronzeAbstract read
In one paragraph

Article in Molecular microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Unveiling the stealthy tactics: mycoplasma's immune evasion strategies.Frontiers in cellular and infection microbiology · 2023
    Review
  3. Review
  4. TheAntibiotics (Basel, Switzerland) · 2021
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Activation of σ20-dependent recombination and horizontal gene transfer in Mycoplasma genitalium.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Indian journal of sexually transmitted diseases and AIDS
    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

2 authors at 1 institution in 1 country.

Raul BurgosDepartment of Medicine, Division of Infectious Diseases, University of Washington, Seattle, WA, 98104, USA.
Patricia A Totten
University of Washington · US

Funding

Mycoplasma genitalium Antigenic VariationR56AI071175 · NIAID · UNIVERSITY OF WASHINGTON · PI TOTTEN, PATRICIA A · 2008 to 2009
$613k
Recombination in a Minimal OrganismR21AI097702 · NIAID · UNIVERSITY OF WASHINGTON · PI TOTTEN, PATRICIA A · 2012 to 2013
$412k
NIAID NIH HHS R21 AI097702NIAID NIH HHS R21AI097702NIAID NIH HHS R56 AI071175NIAID NIH HHS R56AI071175
6 · The paper itself

Abstract

The human pathogen Mycoplasma genitalium employs homologous recombination to generate antigenic diversity in the immunodominant MgpB and MgpC proteins. Only recently, some of the molecular factors involved in this process have been characterized, but nothing is known about its regulation. Here, we show that M. genitalium expresses N-terminally truncated RecA isoforms via alternative translation initiation, but only the full-length protein is essential for gene variation. We also demonstrate that overexpression of MG428 positively regulates the expression of recombination genes, including recA, ruvA, ruvB and ORF2, a gene of unknown function co-transcribed with ruvAB. The co-ordinated induction of these genes correlated with an increase of mgpBC gene variation. In contrast, cells lacking MG428 were unable to generate variants despite expressing normal levels of RecA. Similarly, deletion analyses of the recA upstream region defined sequences required for gene variation without abolishing RecA expression. The requirement of these sequences is consistent with the presence of promoter elements associated with MG428-dependent recA induction. Sequences upstream of recA also influence the relative abundance of RecA isoforms, possibly through translational regulation. Overall, these results suggest that MG428 is a positive regulator of recombination and that precise control of recA expression is required to initiate mgpBC variation.

Indexed as

Gene Expression Regulation, BacterialRecombination, GeneticAmino Acid SequenceBacterial ProteinsGene DeletionGene Expression ProfilingMolecular Sequence DataMycoplasma genitaliumRecombinasesSequence AlignmentTranscription FactorsBacterial ProteinsRecombinasesTranscription Factors

Identifiers

PMID25138908
PMCPMC4203379
OpenAlexW2104493229

What OpenQuestion holds

Textmetadata
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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.