Evidence map›Paper›PMID 24463524›Full record

ArticleNature2014

Sequential evolution of bacterial morphology by co-option of a developmental regulator.

Chao Jiang, Pamela J B Brown, Adrien Ducret, Yves V Brun

Open access · greenAbstract read
In one paragraph

Article in Nature, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 73 citations in OpenAlex.

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  14. Cryogenic single-molecule fluorescence annotations for electron tomography reveal in situ organization of key proteins inProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Article
  16. Article
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  18. Asymmetric division yields progeny cells with distinct modes of regulating cell cycle-dependent chromosome methylation.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Chao JiangDepartment of Biology, Indiana University, Bloomington, Indiana 47405, USA.
Pamela J B Brown1] Department of Biology, Indiana University, Bloomington, Indiana 47405, USA [2] Division of Biological Sciences, University of Missouri, Columbia, Missouri 65211, USA.
Adrien DucretDepartment of Biology, Indiana University, Bloomington, Indiana 47405, USA.
Yves V BrunDepartment of Biology, Indiana University, Bloomington, Indiana 47405, USA.
Indiana University Bloomington · US

Funding

GLOBAL CONTROL OF DIFFERENTIATION IN CAULOBACTERR01GM051986 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI BRUN, YVES V · 1995 to 2016
$6.0M
Acquisition of a DeltaVision OMX Super-Resolution Imaging SystemS10RR028697 · NCRR · INDIANA UNIVERSITY INDIANAPOLIS · PI WALCZAK, CLAIRE E · 2010 to 2010
$1.2M
Nutrient Uptake by the Stalk of Caulobacter crescentusF32AI072992 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI BROWN, PAMELA JANE BONNER · 2007 to 2009
$148k
NCRR NIH HHS S10 RR028697NCRR NIH HHS S10RR028697-01NIAID NIH HHS AI072992NIAID NIH HHS F32 AI072992NIGMS NIH HHS GM051986NIGMS NIH HHS R01 GM051986
6 · The paper itself

Abstract

What mechanisms underlie the transitions responsible for the diverse shapes observed in the living world? Although bacteria exhibit a myriad of morphologies, the mechanisms responsible for the evolution of bacterial cell shape are not understood. We investigated morphological diversity in a group of bacteria that synthesize an appendage-like extension of the cell envelope called the stalk. The location and number of stalks varies among species, as exemplified by three distinct subcellular positions of stalks within a rod-shaped cell body: polar in the genus Caulobacter and subpolar or bilateral in the genus Asticcacaulis. Here we show that a developmental regulator of Caulobacter crescentus, SpmX, is co-opted in the genus Asticcacaulis to specify stalk synthesis either at the subpolar or bilateral positions. We also show that stepwise evolution of a specific region of SpmX led to the gain of a new function and localization of this protein, which drove the sequential transition in stalk positioning. Our results indicate that changes in protein function, co-option and modularity are key elements in the evolution of bacterial morphology. Therefore, similar evolutionary principles of morphological transitions apply to both single-celled prokaryotes and multicellular eukaryotes.

Indexed as

Biological EvolutionCell PolarityBacteriaBacterial ProteinsCaulobacteraceaeCaulobacter crescentusCell MembraneEvolution, MolecularModels, BiologicalMolecular Sequence DataPhylogenyProtein TransportBacterial Proteins

Identifiers

PMID24463524
PMCPMC4035126
OpenAlexW2071901717

What OpenQuestion holds

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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.