Evidence map›Paper›PMID 23909720›Full record

ArticleMolecular microbiology2013

The DivJ, CbrA and PleC system controls DivK phosphorylation and symbiosis in Sinorhizobium meliloti.

Francesco Pini, Benjamin Frage, Lorenzo Ferri, Nicole J De Nisco, Saswat S Mohapatra, Lucilla Taddei, Antonella Fioravanti, Frederique Dewitte, Marco Galardini, Matteo Brilli and 6 more

Open access · greenAbstract read
In one paragraph

Article in Molecular microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact, top 94% 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

37 citing papers in PubMed, 6 citations in OpenAlex.

  1. Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. TheJournal of bacteriology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. DNA Methylation inmSystems · 2022
    Article
  7. Article
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  11. Review
  12. Article
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  16. Review
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  18. Article
  19. Disulfide cross-linking influences symbiotic activities of nodule peptide NCR247.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  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

16 authors at 4 institutions in 4 countries.

Francesco PiniInterdisciplinary Research Institute USR3078, CNRS-Université Lille Nord de France, 50 avenue de Halley, Villeneuve d'Ascq Cedex, France.
Benjamin Frage
Lorenzo Ferri
Nicole J De Nisco
Saswat S Mohapatra
Lucilla Taddei
Antonella Fioravanti
Frederique Dewitte
Marco Galardini
Matteo Brilli
Vincent Villeret
Marco Bazzicalupo
Alessio Mengoni
Graham C Walker
Anke Becker
Emanuele G Biondi
University of Florence · ITMassachusetts Institute of Technology · USPhilipps University of Marburg · DECentre National de la Recherche Scientifique · FR

Funding

MOLEULAR GENETICS OF RHIZOBIUM PLASMIDSR01GM031030 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WALKER, GRAHAM C · 1985 to 2020
$8.6M
NIGMS NIH HHS GM31010NIGMS NIH HHS R01 GM031030
6 · The paper itself

Abstract

Sinorhizobium meliloti is a soil bacterium that invades the root nodules it induces on Medicago sativa, whereupon it undergoes an alteration of its cell cycle and differentiates into nitrogen-fixing, elongated and polyploid bacteroid with higher membrane permeability. In Caulobacter crescentus, a related alphaproteobacterium, the principal cell cycle regulator, CtrA, is inhibited by the phosphorylated response regulator DivK. The phosphorylation of DivK depends on the histidine kinase DivJ, while PleC is the principal phosphatase for DivK. Despite the importance of the DivJ in C. crescentus, the mechanistic role of this kinase has never been elucidated in other Alphaproteobacteria. We show here that the histidine kinases DivJ together with CbrA and PleC participate in a complex phosphorylation system of the essential response regulator DivK in S. meliloti. In particular, DivJ and CbrA are involved in DivK phosphorylation and in turn CtrA inactivation, thereby controlling correct cell cycle progression and the integrity of the cell envelope. In contrast, the essential PleC presumably acts as a phosphatase of DivK. Interestingly, we found that a DivJ mutant is able to elicit nodules and enter plant cells, but fails to establish an effective symbiosis suggesting that proper envelope and/or low CtrA levels are required for symbiosis.

Indexed as

Gene Expression Regulation, BacterialProtein Processing, Post-TranslationalSymbiosisBacterial ProteinsMedicago sativaPhosphorylationSinorhizobium melilotiBacterial Proteins

Identifiers

PMID23909720
PMCPMC3793127
OpenAlexW1563546096

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.