Evidence map›Paper›PMID 25176632›Full record

ArticleCurrent biology : CB2014

Failsafe mechanisms couple division and DNA replication in bacteria.

Heidi A Arjes, Allison Kriel, Nohemy A Sorto, Jared T Shaw, Jue D Wang, Petra Anne Levin

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
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  3. Review
  4. mSystems · 2024
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  5. Creating Polyploid Escherichia Coli and Its Application in Efficient L-Threonine Production.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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  6. Article
  7. Connecting sequence features within the disordered C-terminal linker ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Article
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  11. Article
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  17. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Heidi A ArjesDepartment of Biology, Washington University, St. Louis, MO 63130, USA.
Allison KrielDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Nohemy A SortoDepartment of Chemistry, University of California, Davis, 1 Shields Avenue, Davis, CA 95616, USA.
Jared T ShawDepartment of Chemistry, University of California, Davis, 1 Shields Avenue, Davis, CA 95616, USA.
Jue D WangDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Bacteriology, University of Wisconsin, Madison, WI 53706, USA.
Petra Anne LevinDepartment of Biology, Washington University, St. Louis, MO 63130, USA. Electronic address: plevin@wustl.edu.
University of California, Davis · USWashington University in St. Louis · USBaylor College of Medicine · USUniversity of Wisconsin–Madison · US

Funding

TRAINING PROGRAM IN CELLULAR AND MOLECULAR BIOLOGYT32GM007067 · NIGMS · WASHINGTON UNIVERSITY · PI TRUE-KROB, HEATHER L · 1985 to 2020
$20.4M
TEMPORAL AND SPATIAL CONTROL OF B SUBTILIS CYTOKINESISR01GM064671 · NIGMS · WASHINGTON UNIVERSITY · PI LEVIN, PETRA ANNE · 2002 to 2016
$3.9M
Control of GTP Homeostasis by (p)ppGppR01GM084003 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI WANG, JUE D. · 2009 to 2017
$2.2M
New Research Initiatives and Collaborative Interdisciplinary Research ($10,000-$2R01AI080931 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SHAW, JARED THOMAS · 2010 to 2014
$1.9M
NIGMS NIH HHS R01 GM064671NIGMS NIH HHS R01 GM084003NIGMS NIH HHS T32 GM007067
6 · The paper itself

Abstract

The past 20 years have seen tremendous advances in our understanding of the mechanisms underlying bacterial cytokinesis, particularly the composition of the division machinery and the factors controlling its assembly [1]. At the same time, we understand very little about the relationship between cell division and other cell-cycle events in bacteria. Here we report that inhibiting division in Bacillus subtilis and Staphylococcus aureus quickly leads to an arrest in the initiation of new rounds of DNA replication, followed by a complete arrest in cell growth. Arrested cells are metabolically active but are unable to initiate new rounds of either DNA replication or division when shifted to permissive conditions. Inhibiting DNA replication results in entry into a similar quiescent state in which cells are unable to resume growth or division when returned to permissive conditions. Our data suggest the presence of two failsafe mechanisms: one linking division to the initiation of DNA replication and another linking the initiation of DNA replication to division. These findings contradict the prevailing view of the bacterial cell cycle as a series of coordinated but uncoupled events. Importantly, the terminal nature of the cell-cycle arrest validates the bacterial cell-cycle machinery as an effective target for antimicrobial development.

Indexed as

Cell DivisionDNA ReplicationBacillus subtilisStaphylococcus aureus

Identifiers

PMID25176632
PMCPMC4175050
OpenAlexW2009531024

What OpenQuestion holds

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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.