Evidence map›Paper›PMID 25816203›Full record

ArticlePLoS genetics2015

Transcriptomic profiling of Yersinia pseudotuberculosis reveals reprogramming of the Crp regulon by temperature and uncovers Crp as a master regulator of small RNAs.

Aaron M Nuss, Ann Kathrin Heroven, Barbara Waldmann, Jan Reinkensmeier, Michael Jarek, Michael Beckstette, Petra Dersch

Abstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Journal of bacteriology · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Small RNAs beyond Model Organisms: Have We Only Scratched the Surface?International journal of molecular sciences · 2022
    Article
  13. A Peroxide-Responding sRNA Evolved from a Peroxidase mRNA.Molecular biology and evolution · 2022
    Article
  14. Yersiniabactin contributes to overcoming zinc restriction duringProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
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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

7 authors.

Aaron M NussDepartment of Molecular Infection Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Ann Kathrin HerovenDepartment of Molecular Infection Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Barbara WaldmannDepartment of Molecular Infection Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Jan ReinkensmeierFaculty of Technology and Center for Biotechnology (CeBiTec), Bielefeld University, Germany.
Michael JarekDepartment of Genome Analytics, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Michael BeckstetteDepartment of Molecular Infection Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Petra DerschDepartment of Molecular Infection Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One hallmark of pathogenic yersiniae is their ability to rapidly adjust their life-style and pathogenesis upon host entry. In order to capture the range, magnitude and complexity of the underlying gene control mechanisms we used comparative RNA-seq-based transcriptomic profiling of the enteric pathogen Y. pseudotuberculosis under environmental and infection-relevant conditions. We identified 1151 individual transcription start sites, multiple riboswitch-like RNA elements, and a global set of antisense RNAs and previously unrecognized trans-acting RNAs. Taking advantage of these data, we revealed a temperature-induced and growth phase-dependent reprogramming of a large set of catabolic/energy production genes and uncovered the existence of a thermo-regulated 'acetate switch', which appear to prime the bacteria for growth in the digestive tract. To elucidate the regulatory architecture linking nutritional status to virulence we also refined the CRP regulon. We identified a massive remodelling of the CRP-controlled network in response to temperature and discovered CRP as a transcriptional master regulator of numerous conserved and newly identified non-coding RNAs which participate in this process. This finding highlights a novel level of complexity of the regulatory network in which the concerted action of transcriptional regulators and multiple non-coding RNAs under control of CRP adjusts the control of Yersinia fitness and virulence to the requirements of their environmental and virulent life-styles.

Indexed as

Gene Expression ProfilingCyclic AMPCyclic AMP Receptor ProteinFungal ProteinsGene-Environment InteractionGene Expression Regulation, FungalRegulonRiboswitchRNA, AntisenseTemperatureTranscription Initiation SiteYersinia pseudotuberculosisCyclic AMPCyclic AMP Receptor ProteinFungal ProteinsRiboswitchRNA, Antisense

Identifiers

PMID25816203
PMCPMC4376681

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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.