Evidence map›Paper›PMID 26621053›Full record

ArticleScientific reports2015

Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG.

Rita Figueira, Daniel R Brown, Delfim Ferreira, Matthew J G Eldridge, Lynn Burchell, Zhensheng Pan, Sophie Helaine, Sivaramesh Wigneshweraraj

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–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

28 citing papers in PubMed.

  1. Global proteolysis during starvation governs proteome remodeling and a survival-regrowth trade-off in bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  2. Maltose aids in the growth ofFEMS microbes · 2026
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  6. Serving Two Masters: Effect ofAntibiotics (Basel, Switzerland) · 2023
    Article
  7. Article
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  10. Review
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  13. Phosphoproteome Study ofFrontiers in microbiology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Wide lag time distributions break a trade-off between reproduction and survival in bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  18. Review
  19. The expanded specificity and physiological role of a widespread N-degron recognin.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  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

8 authors.

Rita FigueiraMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.
Daniel R BrownMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.
Delfim FerreiraMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.
Matthew J G EldridgeMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.
Lynn BurchellMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.
Zhensheng PanMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.
Sophie HelaineMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.
Sivaramesh WigneshwerarajMRC Centre for Molecular Microbiology and Infection, Imperial College London, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/G020434/1Medical Research Council MR/J006874/1Medical Research Council MR/M009629/1Wellcome Trust 100958
6 · The paper itself

Abstract

The Escherichia coli eukaryote-like serine/threonine kinase, encoded by yeaG, is expressed in response to diverse stresses, including nitrogen (N) starvation. A role for yeaG in bacterial stress response is unknown. Here we reveal for the first time that wild-type E. coli displays metabolic heterogeneity following sustained periods of N starvation, with the metabolically active population displaying compromised viability. In contrast, such heterogeneity in metabolic activity is not observed in an E. coli ∆yeaG mutant, which continues to exist as a single and metabolically active population and thus displays an overall compromised ability to survive sustained periods of N starvation. The mechanism by which yeaG acts, involves the transcriptional repression of two toxin/antitoxin modules, mqsR/mqsA and dinJ/yafQ. This, consequently, has a positive effect on the expression of rpoS, the master regulator of the general bacterial stress response. Overall, results indicate that yeaG is required to fully execute the rpoS-dependent gene expression program to allow E. coli to adapt to sustained N starvation and unravels a novel facet to the regulatory basis that underpins adaptive response to N stress.

Indexed as

Adaptation, PhysiologicalBacterial ProteinsBacterial ToxinsDNA-Binding ProteinsEscherichia coli K12Escherichia coli ProteinsGene DeletionNitrogenProtein Serine-Threonine KinasesSigma FactorBacterial ProteinsBacterial ToxinsDinJ protein, E coliDNA-Binding ProteinsEscherichia coli ProteinsMqsA protein, E coliMqsR protein, E coliNitrogenProtein Serine-Threonine KinasesSigma Factorsigma factor KatF protein, BacteriaYafQ protein, E coliYeaG protein, E coli

Identifiers

PMID26621053
PMCPMC4664914

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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.