Evidence map›Paper›PMID 21799784›Full record

ArticlePloS one2011

A defined terminal region of the E. coli chromosome shows late segregation and high FtsK activity.

Marie Deghorain, Carine Pagès, Jean-Christophe Meile, Mathieu Stouf, Hervé Capiaux, Romain Mercier, Christian Lesterlin, Bernard Hallet, François Cornet

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. How Xer-exploiting mobile elements overcome cellular control.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  9. Structures of the nucleoid occlusion protein SlmA bound to DNA and the C-terminal domain of the cytoskeletal protein FtsZ.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  10. Defining the rate-limiting processes of bacterial cytokinesis.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  11. Review
  12. Article
  13. Cell cycle regulation by the bacterial nucleoid.Current opinion in microbiology · 2014
    Review
  14. Review
  15. FtsK actively segregates sister chromosomes in Escherichia coli.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  16. Article
  17. Molecular motors for DNA translocation in prokaryotes.Current opinion in biotechnology · 2012
    Review
  18. Article
  19. Single-molecule imaging of DNA curtains reveals mechanisms of KOPS sequence targeting by the DNA translocase FtsK.Proceedings of the National Academy of Sciences of the United States of America · 2012
    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

9 authors at 3 institutions in 2 countries.

Marie DeghorainLaboratoire de Microbiologie et de Génétique Moléculaire, CNRS, Toulouse, France.
Carine Pagès
Jean-Christophe Meile
Mathieu Stouf
Hervé Capiaux
Romain Mercier
Christian Lesterlin
Bernard Hallet
François Cornet
Laboratoire de Microbiologie et Génétique Moléculaires · FRCentre National de la Recherche Scientifique · FRUCLouvain · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe FtsK DNA-translocase controls the last steps of chromosome segregation in E. coli. It translocates sister chromosomes using the KOPS DNA motifs to orient its activity, and controls the resolution of dimeric forms of sister chromosomes by XerCD-mediated recombination at the dif site and their decatenation by TopoIV. METHODOLOGY: We have used XerCD/dif recombination as a genetic trap to probe the interaction of FtsK with loci located in different regions of the chromosome. This assay revealed that the activity of FtsK is restricted to a ∼400 kb terminal region of the chromosome around the natural position of the dif site. Preferential interaction with this region required the tethering of FtsK to the division septum via its N-terminal domain as well as its translocation activity. However, the KOPS-recognition activity of FtsK was not required. Displacement of replication termination outside the FtsK high activity region had no effect on FtsK activity and deletion of a part of this region was not compensated by its extension to neighbouring regions. By observing the fate of fluorescent-tagged loci of the ter region, we found that segregation of the FtsK high activity region is delayed compared to that of its adjacent regions. SIGNIFICANCE: Our results show that a restricted terminal region of the chromosome is specifically dedicated to the last steps of chromosome segregation and to their coupling with cell division by FtsK.

Indexed as

Chromosome SegregationChromosomes, BacterialDNA, BacterialEscherichia coli K12Escherichia coli ProteinsMembrane ProteinsNucleotide MotifsProtein Structure, TertiarySequence DeletionDNA, BacterialEscherichia coli ProteinsFtsK protein, E coliMembrane Proteins

Identifiers

PMID21799784
PMCPMC3140498
OpenAlexW2059770256

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.