Evidence map›Paper›PMID 33093592›Full record

ArticleScientific reports2020

Overexpression of the third H-NS paralogue H-NS2 compensates fitness loss in hns mutants of the enteroaggregative Escherichia coli strain 042.

A Prieto, M Bernabeu, L Falgenhauer, T Chakraborty, M Hüttener, A Juárez

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

6 authors at 3 institutions in 2 countries.

A PrietoDepartment of Genetics, Microbiology and Statistics, University of Barcelona, Barcelona, Spain.
M BernabeuDepartment of Genetics, Microbiology and Statistics, University of Barcelona, Barcelona, Spain.
L FalgenhauerInstitute of Hygiene and Environmental Medicine, Justus Liebig University Giessen, Schubertstrasse 81, 35392, Giessen, Germany.
T ChakrabortyGerman Center for Infection Research DZIF, Partner Site Giessen-Marburg-Langen, Campus, Giessen, Germany.
M HüttenerDepartment of Genetics, Microbiology and Statistics, University of Barcelona, Barcelona, Spain.
A JuárezDepartment of Genetics, Microbiology and Statistics, University of Barcelona, Barcelona, Spain. ajuarez@ub.edu.
Universitat de Barcelona · ESGerman Center for Infection Research · DEJustus-Liebig-Universität Gießen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Members of the H-NS protein family play a role both in the chromosome architecture and in the regulation of gene expression in bacteria. The genomes of the enterobacteria encode an H-NS paralogue, the StpA protein. StpA displays specific regulatory properties and provides a molecular backup for H-NS. Some enterobacteria also encode third H-NS paralogues. This is the case of the enteroaggregative E. coli (EAEC) strain 042, which encodes the hns, stpA and hns2 genes. We provide in this paper novel information about the role of the H-NS2 protein in strain 042. A C > T transition in the hns2 promoter leading to increased H-NS2 expression is readily selected in hns mutants. Increased H-NS2 expression partially compensates for H-NS loss. H-NS2 levels are critical for the strain 042 fitness. Under some circumstances, high H-NS2 expression levels dictated by the mutant hns2 promoter can be deleterious. The selection of T > C revertants or of clones harboring insertional inactivations of the hns2 gene can then occur. Temperature also plays a relevant role in the H-NS2 regulatory activity. At 37 °C, H-NS2 targets a subset of the H-NS repressed genes contributing to their silencing. When temperature drops to 25 °C, the repressory ability of H-NS2 is significantly reduced. At low temperature, H-NS plays the main repressory role.

Indexed as

Gene Expression Regulation, BacterialGenetic FitnessMutationChromosomes, BacterialEscherichia coliEscherichia coli ProteinsFimbriae ProteinsEscherichia coli ProteinsFimbriae ProteinsFimG protein, E coli

Identifiers

PMID33093592
PMCPMC7582179
OpenAlexW3093815415

What OpenQuestion holds

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Registered trials

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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.