Evidence map›Paper›PMID 26590283›Full record

ArticleApplied and environmental microbiology2016

MvaT Family Proteins Encoded on IncP-7 Plasmid pCAR1 and the Host Chromosome Regulate the Host Transcriptome Cooperatively but Differently.

Choong-Soo Yun, Yurika Takahashi, Masaki Shintani, Toshiharu Takeda, Chiho Suzuki-Minakuchi, Kazunori Okada, Hisakazu Yamane, Hideaki Nojiri

Abstract read
In one paragraph

Article in Applied and environmental microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. The H-NS homologues MvaT and MvaU repress CRISPR-Cas inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  3. Article
  4. Why do plasmids manipulate the expression of bacterial phenotypes?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Reconsidering plasmid maintenance factors for computational plasmid design.Computational and structural biotechnology journal · 2019
    Review
  11. Article
  12. 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

8 authors.

Choong-Soo YunBiotechnology Research Center, The University of Tokyo, Tokyo, Japan Agricultural Bioinformatics Research Unit, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Yurika TakahashiBiotechnology Research Center, The University of Tokyo, Tokyo, Japan Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University, Imizu, Toyama, Japan.
Masaki ShintaniBiotechnology Research Center, The University of Tokyo, Tokyo, Japan Applied Chemistry and Biochemical Engineering Course, Department of Engineering, Graduate School of Integrated Science and Technology, Shizuoka University, Hamamatsu, Shizuoka, Japan.
Toshiharu TakedaBiotechnology Research Center, The University of Tokyo, Tokyo, Japan.
Chiho Suzuki-MinakuchiBiotechnology Research Center, The University of Tokyo, Tokyo, Japan.
Kazunori OkadaBiotechnology Research Center, The University of Tokyo, Tokyo, Japan.
Hisakazu YamaneBiotechnology Research Center, The University of Tokyo, Tokyo, Japan.
Hideaki NojiriBiotechnology Research Center, The University of Tokyo, Tokyo, Japan Agricultural Bioinformatics Research Unit, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan anojiri@mail.ecc.u-tokyo.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MvaT proteins are members of the H-NS family of proteins in pseudomonads. The IncP-7 conjugative plasmid pCAR1 carries an mvaT-homologous gene, pmr. In Pseudomonas putida KT2440 bearing pCAR1, pmr and the chromosomally carried homologous genes, turA and turB, are transcribed at high levels, and Pmr interacts with TurA and TurB in vitro. In the present study, we clarified how the three MvaT proteins regulate the transcriptome of P. putida KT2440(pCAR1). Analyses performed by a modified chromatin immunoprecipitation assay with microarray technology (ChIP-chip) suggested that the binding regions of Pmr, TurA, and TurB in the P. putida KT2440(pCAR1) genome are almost identical; nevertheless, transcriptomic analyses using mutants with deletions of the genes encoding the MvaT proteins during the log and early stationary growth phases clearly suggested that their regulons were different. Indeed, significant regulon dissimilarity was found between Pmr and the other two proteins. Transcription of a larger number of genes was affected by Pmr deletion during early stationary phase than during log phase, suggesting that Pmr ameliorates the effects of pCAR1 on host fitness more effectively during the early stationary phase. Alternatively, the similarity of the TurA and TurB regulons implied that they might play complementary roles as global transcriptional regulators in response to plasmid carriage.

Indexed as

Gene Expression Regulation, BacterialTranscriptomeBacterial ProteinsChromosomes, BacterialDNA, BacterialGene Expression ProfilingGenetic FitnessGenome, BacterialImmunoprecipitationMicroarray AnalysisPlasmidsPseudomonas putidaRegulonSequence DeletionTrans-ActivatorsBacterial ProteinsDNA, BacterialMvaT protein, PseudomonasTrans-Activators

Identifiers

PMID26590283
PMCPMC4725287

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.