Evidence map›Paper›PMID 19897644›Full record

ArticleJournal of bacteriology2010

P1 plasmid segregation: accurate redistribution by dynamic plasmid pairing and separation.

Manjistha Sengupta, Henrik Jorck Nielsen, Brenda Youngren, Stuart Austin

Abstract read
In one paragraph

Article in Journal of bacteriology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

47 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. 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
  6. Review
  7. Article
  8. VirB, a key transcriptional regulator ofbioRxiv : the preprint server for biology · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Manjistha SenguptaGene Regulation and Chromosome Biology Laboratory, National Cancer Institute, CCR, NCI-Frederick, Frederick, MD 21702-1201, USA.
Henrik Jorck Nielsen
Brenda Youngren
Stuart Austin

Funding

The automated measurement of foci in fluorescence microscopyZIHBC011161 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AUSTIN, STUART J · 2009 to 2014
$1.4M
The Maintenance of Plasmids in Pathogenic OrganismsZIABC010558 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AUSTIN, STUART J · 2009 to 2011
$1.0M
Intramural NIH HHS
6 · The paper itself

Abstract

Low-copy-number plasmids, such as P1 and F, encode a type Ia partition system (P1par or Fsop) for active segregation of copies to daughter cells. Typical descriptions show a single central plasmid focus dividing and the products moving to the cell quarter regions, ensuring segregation. However, using improved optical and analytical tools and large cell populations, we show that P1 plasmid foci are very broadly distributed. Moreover, under most growth conditions, more than two foci are frequently present. Each focus contains either one or two plasmid copies. Replication and focus splitting occur at almost any position in the cell. The products then move rapidly apart for approximately 40% of the cell length. They then tend to maintain their relative positions. The segregating foci often pass close to or come to rest close to other foci in the cell. Foci frequently appear to fuse during these encounters. Such events occur several times in each cell and cell generation on average. We argue that foci pair with their neighbors and then actively separate again. The net result is an approximately even distribution of foci along the long cell axis on average. We show mathematically that trans-pairing and active separation could greatly increase the accuracy of segregation and would produce the distributions of foci that we observe. Plasmid pairing and separation may constitute a novel fine-tuning mechanism that takes the basic pattern created when plasmids separate after replication and converts it to a roughly even pattern that greatly improves the fidelity of plasmid segregation.

Indexed as

Cell DivisionDNA ReplicationBacteriophage P1DNA, ViralEscherichia coliModels, BiologicalPlasmidsDNA, Viral

Identifiers

PMID19897644
PMCPMC2820840

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.