Evidence map›Paper›PMID 24349499›Full record

ArticlePloS one2013

The bZIP transcription factor Fgap1 mediates oxidative stress response and trichothecene biosynthesis but not virulence in Fusarium graminearum.

Mathilde Montibus, Christine Ducos, Marie-Noelle Bonnin-Verdal, Jorg Bormann, Nadia Ponts, Florence Richard-Forget, Christian Barreau

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
11.1field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Global Transcriptomic Changes Elicited byJournal of fungi (Basel, Switzerland) · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Microbe Related Chemical Signalling and Its Application in Agriculture.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. International journal of molecular sciences · 2022
    Article
  18. Article
  19. The NADPH Oxidase A ofJournal of fungi (Basel, Switzerland) · 2021
    Article
  20. 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

7 authors at 2 institutions in 2 countries.

Mathilde MontibusInstitut National de la Recherche Agronomique, Unité de Recherche 1264 MycSA, Villenave d'Ornon, France.
Christine DucosInstitut National de la Recherche Agronomique, Unité de Recherche 1264 MycSA, Villenave d'Ornon, France.
Marie-Noelle Bonnin-VerdalInstitut National de la Recherche Agronomique, Unité de Recherche 1264 MycSA, Villenave d'Ornon, France.
Jorg BormannUniversity of Hamburg, Biocenter Klein Flottbek, Department of Molecular Phytopathology and Genetics, Hamburg, Germany.
Nadia PontsInstitut National de la Recherche Agronomique, Unité de Recherche 1264 MycSA, Villenave d'Ornon, France.
Florence Richard-ForgetInstitut National de la Recherche Agronomique, Unité de Recherche 1264 MycSA, Villenave d'Ornon, France.
Christian BarreauInstitut National de la Recherche Agronomique, Unité de Recherche 1264 MycSA, Villenave d'Ornon, France ; Centre National de la Recherche Scientifique, Unité de Recherche 1264 MycSA, Villenave d'Ornon, France.
Mycologie et Sécurité des Aliments · FRUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Redox sensing is of primary importance for fungi to cope with oxidant compounds found in their environment. Plant pathogens are particularly subject to the oxidative burst during the primary steps of infection. In the budding yeast Saccharomyces cerevisiae, it is the transcription factor Yap1 that mediates the response to oxidative stress via activation of genes coding for detoxification enzymes. In the cereal pathogen Fusarium graminearum, Fgap1 a homologue of Yap1 was identified and its role was investigated. During infection, this pathogen produces mycotoxins belonging to the trichothecenes family that accumulate in the grains. The global regulation of toxin biosynthesis is not completely understood. However, it is now clearly established that an oxidative stress activates the production of toxins by F. graminearum. The involvement of Fgap1 in this activation was investigated. A deleted mutant and a strain expressing a truncated constitutive form of Fgap1 were constructed. None of the mutants was affected in pathogenicity. The deleted mutant showed higher level of trichothecenes production associated with overexpression of Tri genes. Moreover activation of toxin accumulation in response to oxidative stress was no longer observed. Regarding the mutant with the truncated constitutive form of Fgap1, toxin production was strongly reduced. Expression of oxidative stress response genes was not activated in the deleted mutant and expression of the gene encoding the mitochondrial superoxide dismutase MnSOD1 was up-regulated in the mutant with the truncated constitutive form of Fgap1. Our results demonstrate that Fgap1 plays a key role in the link between oxidative stress response and F. graminearum secondary metabolism.

Indexed as

Basic-Leucine Zipper Transcription FactorsFungal ProteinsFusariumGene Expression Regulation, FungalOxidative StressTrichothecenesBasic-Leucine Zipper Transcription FactorsFungal ProteinsTrichothecenes

Identifiers

PMID24349499
PMCPMC3861502
OpenAlexW1994247089

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.