Evidence map›Paper›PMID 9465034›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

An essential, multicomponent signal transduction pathway required for cell cycle regulation in Caulobacter.

J Wu, N Ohta, A Newton

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 106 citations in OpenAlex.

  1. Review
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  15. Article
  16. Getting in the loop: regulation of development in Caulobacter crescentus.Microbiology and molecular biology reviews : MMBR · 2010
    Review
  17. Article
  18. Synchronization of chromosome dynamics and cell division in bacteria.Cold Spring Harbor perspectives in biology · 2010
    Review
  19. Article
  20. Cellular polarity in prokaryotic organisms.Cold Spring Harbor perspectives in biology · 2009
    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

3 authors at 1 institution in 1 country.

J WuDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
N Ohta
A Newton
Princeton University · US

Funding

REGULATION OF DEVELOPMENT IN CAULOBACTER CRESCENTUSR01GM022299 · NIGMS · PRINCETON UNIVERSITY · PI NEWTON, AUSTIN · 1985 to 1999
–
NIGMS NIH HHS GM22299
6 · The paper itself

Abstract

Cell differentiation and division in Caulobacter crescentus are regulated by a signal transduction pathway mediated by the histidine kinase DivJ and the essential response regulator DivK. Here we report genetic and biochemical evidence that the DivJ and DivK proteins function to control the activity of CtrA, a response regulator required for multiple cell cycle events, including flagellum biosynthesis, DNA replication, and cell division. Temperature-sensitive sokA (suppressor of divK) alleles were isolated as extragenic suppressors of a cold-sensitive divK mutation and mapped to the C terminus of the CtrA protein. The sokA alleles also suppress the lethal phenotype of a divK gene disruption and the cold-sensitive cell division phenotype of divJ mutants. The relationship between these signal transduction components and their target was further defined by demonstrating that the purified DivJ kinase phosphorylates CtrA, as well as DivK. Our studies also showed that phospho-CtrA activates transcription in vitro from the class II flagellar genes and that their promoters are recognized by the principal C. crescentus sigma factor sigma73. We propose that an essential signal transduction pathway mediated by DivJ, DivK, and CtrA coordinates cell cycle and developmental events in C. crescentus by regulating the level of CtrA phosphorylation and transcription from sigma73-dependent class II gene promoters. Our results suggest that an unidentified phosphotransfer protein or kinase (X) is responsible for phosphoryl group transfer to CtrA in the proposed DivJ --> DivK --> X --> CtrA phosphorelay pathway.

Indexed as

DNA-Binding ProteinsTranscription FactorsAllelesBacterial ProteinsBase SequenceCaulobacter crescentusCell CycleGene Expression Regulation, BacterialGene Expression Regulation, DevelopmentalGenes, BacterialGenes, SuppressorGenetic Complementation TestHistidine KinaseMolecular Sequence DataPhosphorylationPromoter Regions, GeneticBacterial ProteinsCtrA protein, CaulobacterDivK protein, Caulobacter crescentusDNA-Binding ProteinsHistidine KinaseProtein KinasesSigma FactorTranscription Factors

Identifiers

PMID9465034
PMCPMC19037
OpenAlexW2089947295

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.