Evidence map›Paper›PMID 28034957›Full record

ArticleNucleic acids research2017

A three-dimensional ParF meshwork assembles through the nucleoid to mediate plasmid segregation.

Brett N McLeod, Gina E Allison-Gamble, Madhuri T Barge, Nam K Tonthat, Maria A Schumacher, Finbarr Hayes, Daniela Barillà

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Coordinating plasmid partition with bacterial chromosome segregation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Plasmid partitioning driven by collective migration of ParA between nucleoid lobes.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. CTP andeLife · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  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 2 countries.

Brett N McLeodDepartment of Biology, University of York, Wentworth Way, York YO10 5DD, UK.
Gina E Allison-GambleDepartment of Biology, University of York, Wentworth Way, York YO10 5DD, UK.
Madhuri T BargeDepartment of Biology, University of York, Wentworth Way, York YO10 5DD, UK.
Nam K TonthatDepartment of Biochemistry, Duke University Medical Center, Duke University, Durham, NC 27710, USA.
Maria A SchumacherDepartment of Biochemistry, Duke University Medical Center, Duke University, Durham, NC 27710, USA.
Finbarr HayesFaculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9PL, UK.
Daniela BarillàDepartment of Biology, University of York, Wentworth Way, York YO10 5DD, UK.
University of York · GBDuke University Hospital · USUniversity of Manchester · GB

Funding

Assembly and partition mechanism of Walker-box based segregation machineryR01GM115563 · NIGMS · DUKE UNIVERSITY · PI SCHUMACHER, MARIA · 2015 to 2018
$1.2M
NIGMS NIH HHS R01 GM115563
6 · The paper itself

Abstract

Genome segregation is a fundamental step in the life cycle of every cell. Most bacteria rely on dedicated DNA partition proteins to actively segregate chromosomes and low copy-number plasmids. Here, by employing super resolution microscopy, we establish that the ParF DNA partition protein of the ParA family assembles into a three-dimensional meshwork that uses the nucleoid as a scaffold and periodically shuttles between its poles. Whereas ParF specifies the territory for plasmid trafficking, the ParG partner protein dictates the tempo of ParF assembly cycles and plasmid segregation events by stimulating ParF adenosine triphosphate hydrolysis. Mutants in which this ParG temporal regulation is ablated show partition deficient phenotypes as a result of either altered ParF structure or dynamics and indicate that ParF nucleoid localization and dynamic relocation, although necessary, are not sufficient per se to ensure plasmid segregation. We propose a Venus flytrap model that merges the concepts of ParA polymerization and gradient formation and speculate that a transient, dynamic network of intersecting polymers that branches into the nucleoid interior is a widespread mechanism to distribute sizeable cargos within prokaryotic cells.

Indexed as

1-Acylglycerol-3-Phosphate O-AcyltransferaseDNAEscherichia coliEscherichia coli ProteinsMicroscopy, FluorescenceMutationPlasmidsRepressor ProteinsTime-Lapse Imaging1-Acylglycerol-3-Phosphate O-AcyltransferaseDNAEscherichia coli ProteinsParG protein, E coliplsC protein, E coliRepressor Proteins

Identifiers

PMID28034957
PMCPMC5389482
OpenAlexW2565218132

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.