Evidence map›Paper›PMID 30422330›Full record

ArticleMolecular microbiology2019

Protease-deficient SOS constitutive cells have RecN-dependent cell division phenotypes.

Alyson R Warr, Anastasiia N Klimova, Amy N Nwaobasi, Steven J Sandler

Open access · greenAbstract read
In one paragraph

Article in Molecular microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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  5. An Epistasis Analysis ofGenetics · 2020
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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

4 authors at 1 institution in 1 country.

Alyson R WarrDepartment of Microbiology, Morrill Science Center IV N203, University of Massachusetts Amherst, Amherst, MA, 01003, USA.
Anastasiia N KlimovaMolecular and Cellular Biology Program, University of Massachusetts Amherst, Amherst, MA, 01003, USA.
Amy N NwaobasiDepartment of Microbiology, Morrill Science Center IV N203, University of Massachusetts Amherst, Amherst, MA, 01003, USA.
Steven J SandlerDepartment of Microbiology, Morrill Science Center IV N203, University of Massachusetts Amherst, Amherst, MA, 01003, USA.
University of Massachusetts Amherst · US

Funding

Structure and Function of the Bacterial PrimosomeR01GM098885 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI James L Keck · 2012 to 2026
$4.0M
NIGMS NIH HHS R01 GM098885NIH HHS GM098885
6 · The paper itself

Abstract

In Escherichia coli, after DNA damage, the SOS response increases the transcription (and protein levels) of approximately 50 genes. As DNA repair ensues, the level of transcription returns to homeostatic levels. ClpXP and other proteases return the high levels of several SOS proteins to homeostasis. When all SOS genes are constitutively expressed and many SOS proteins are stabilized by the removal of ClpXP, microscopic analysis shows that cells filament, produce mini-cells and have branching protrusions along their length. The only SOS gene required (of 19 tested) for the cell length phenotype is recN. RecN is a member of the Structural Maintenance of Chromosome (SMC) class of proteins. It can hold pieces of DNA together and is important for double-strand break repair (DSBR). RecN is degraded by ClpXP. Overexpression of recN

Indexed as

Cell DivisionSOS Response, GeneticsBacterial ProteinsDNA Restriction EnzymesEscherichia coliMicroscopyPeptide HydrolasesPhenotypeBacterial ProteinsDNA Restriction EnzymesPeptide HydrolasesRecN protein, Bacteria

Identifiers

PMID30422330
PMCPMC6368896
OpenAlexW2900536401

What OpenQuestion holds

Textmetadata
LicenceTDM
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.