Evidence map›Paper›PMID 25255436›Full record

ArticlePLoS genetics2014

Differential management of the replication terminus regions of the two Vibrio cholerae chromosomes during cell division.

Gaëlle Demarre, Elisa Galli, Leila Muresan, Evelyne Paly, Ariane David, Christophe Possoz, François-Xavier Barre

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.4field-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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  12. Review
  13. The TLCΦ satellite phage harbors a Xer recombination activation factor.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  14. Article
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  17. Review
  18. The Divided Bacterial Genome: Structure, Function, and Evolution.Microbiology and molecular biology reviews : MMBR · 2017
    Review
  19. Article
  20. Article
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

7 authors at 3 institutions in 1 country.

Gaëlle DemarreCNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
Elisa GalliCNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
Leila MuresanCNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
Evelyne PalyCNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
Ariane DavidCNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
Christophe PossozCNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
François-Xavier BarreCNRS, Centre de Génétique Moléculaire, Gif-sur-Yvette, France; Université Paris-Sud, Orsay, France.
Centre de Génétique Moléculaire · FRCentre National de la Recherche Scientifique · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The replication terminus region (Ter) of the unique chromosome of most bacteria locates at mid-cell at the time of cell division. In several species, this localization participates in the necessary coordination between chromosome segregation and cell division, notably for the selection of the division site, the licensing of the division machinery assembly and the correct alignment of chromosome dimer resolution sites. The genome of Vibrio cholerae, the agent of the deadly human disease cholera, is divided into two chromosomes, chrI and chrII. Previous fluorescent microscopy observations suggested that although the Ter regions of chrI and chrII replicate at the same time, chrII sister termini separated before cell division whereas chrI sister termini were maintained together at mid-cell, which raised questions on the management of the two chromosomes during cell division. Here, we simultaneously visualized the location of the dimer resolution locus of each of the two chromosomes. Our results confirm the late and early separation of chrI and chrII Ter sisters, respectively. They further suggest that the MatP/matS macrodomain organization system specifically delays chrI Ter sister separation. However, TerI loci remain in the vicinity of the cell centre in the absence of MatP and a genetic assay specifically designed to monitor the relative frequency of sister chromatid contacts during constriction suggest that they keep colliding together until the very end of cell division. In contrast, we found that even though it is not able to impede the separation of chrII Ter sisters before septation, the MatP/matS macrodomain organization system restricts their movement within the cell and permits their frequent interaction during septum constriction.

Indexed as

Cell DivisionChromosomes, BacterialDNA ReplicationBacterial ProteinsChromosomal Proteins, Non-HistoneChromosome SegregationRecombination, GeneticSister Chromatid ExchangeTime-Lapse ImagingVibrio choleraeBacterial ProteinsChromosomal Proteins, Non-Histone

Identifiers

PMID25255436
PMCPMC4177673
OpenAlexW1990702669

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.