Evidence map›Paper›PMID 7592388›Full record

ArticleJournal of bacteriology1995

Identification of a novel response regulator required for the swarmer-to-stalked-cell transition in Caulobacter crescentus.

G B Hecht, A Newton

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of bacteriology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

85 citing papers in PubMed, 206 citations in OpenAlex.

  1. Review
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  3. Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  7. ACS synthetic biology · 2023
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  8. Review
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  18. Analysis ofJournal of bacteriology · 2019
    Article
  19. Article
  20. Article

25 more citing papers are in PubMed but not listed here.

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.

G B HechtLewis Thomas Laboratory, Department of Molecular Biology, Princeton University, New Jersey 08544-1014, USA.
A Newton
Princeton University · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
NIGMS NIH HHS GM07388-15
6 · The paper itself

Abstract

The onset of motility late in the Caulobacter crescentus cell cycle depends on a signal transduction pathway mediated by the histidine kinase PleC and response regulator DivK. We now show that pleD, whose function is required for the subsequent loss of motility and stalk formation by the motile swarmer cell, encodes a 454-residue protein with tandem N-terminal response regulator domains D1 and D2 and a novel C-terminal GGDEF domain. The identification of pleD301, a semidominant suppressor of the pleC Mot phenotype, as a mutation predicted to result in a D-53-->G change in the D1 domain supports a role for phosphorylation in the PleD regulator. Disruptions constructed in the pleD open reading frame demonstrated that the gene is not essential and that the pleC phenotype can also be suppressed by a recessive, loss-of-function mutation. These results suggest that PleD is part of a signal transduction pathway controlling stalked-cell differentiation early in the C. crescentus cell cycle.

Indexed as

AllelesAmino Acid SequenceBacterial ProteinsBase SequenceCaulobacter crescentusCell CycleCell DifferentiationCloning, MolecularGenes, BacterialGenetic Complementation TestModels, BiologicalMolecular Sequence DataPhenotypeSequence Analysis, DNASequence Homology, Amino AcidSignal TransductionBacterial ProteinsDivK protein, Caulobacter crescentusPleD protein, Caulobacter crescentus

Identifiers

PMID7592388
PMCPMC177463
OpenAlexW2161465177

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.