Evidence map›Paper›PMID 30130575›Full record

ArticleFungal genetics and biology : FG & B2018

The epigenetic reader SntB regulates secondary metabolism, development and global histone modifications in Aspergillus flavus.

Brandon T Pfannenstiel, Claudio Greco, Andrew T Sukowaty, Nancy P Keller

Abstract read
In one paragraph

Article in Fungal genetics and biology : FG & B, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. SntB Affects Growth to Regulate Infecting Potential inJournal of fungi (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Article
  5. Polyketides as Secondary Metabolites from the GenusJournal of fungi (Basel, Switzerland) · 2023
    Review
  6. Review
  7. Genetic Regulation of Mycotoxin Biosynthesis.Journal of fungi (Basel, Switzerland) · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. TheJournal of fungi (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Review
  15. Review
  16. Microevolution in the pansecondary metabolome ofProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Article
  18. Review
  19. 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

4 authors.

Brandon T PfannenstielDepartment of Genetics, University of Wisconsin-Madison, Madison, WI, USA.
Claudio GrecoDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA.
Andrew T SukowatyDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA.
Nancy P KellerDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA; Department of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA. Electronic address: npkeller@wisc.edu.

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007133 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PERNA, NICOLE T · 1985 to 2023
$16.5M
Comprehensive analysis of NRPS-derived metabolomes of three Aspergillus speciesR01GM112739 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI KELLER, NANCY P · 2015 to 2023
$2.8M
NIGMS NIH HHS R01 GM112739NIGMS NIH HHS T32 GM007133
6 · The paper itself

Abstract

Due to the role, both beneficial and harmful, that fungal secondary metabolites play in society, the study of their regulation is of great importance. Genes for any one secondary metabolite are contiguously arranged in a biosynthetic gene cluster (BGC) and subject to regulation through the remodeling of chromatin. Histone modifying enzymes can place or remove post translational modifications (PTM) on histone tails which influences how tight or relaxed the chromatin is, impacting transcription of BGCs. In a recent forward genetic screen, the epigenetic reader SntB was identified as a transcriptional regulator of the sterigmatocystin BGC in A. nidulans, and regulated the related metabolite aflatoxin in A. flavus. In this study we investigate the role of SntB in the plant pathogen A. flavus by analyzing both ΔsntB and overexpression sntB genetic mutants. Deletion of sntB increased global levels of H3K9K14 acetylation and impaired several developmental processes including sclerotia formation, heterokaryon compatibility, secondary metabolite synthesis, and ability to colonize host seeds; in contrast the overexpression strain displayed fewer phenotypes. ΔsntB developmental phenotypes were linked with SntB regulation of NosA, a transcription factor regulating the A. flavus cell fusion cascade.

Indexed as

AcetylationAflatoxinsAspergillus flavusEpigenesis, GeneticFungal ProteinsGene Expression Regulation, FungalHistonesMutationPromoter Regions, GeneticReproductionSecondary MetabolismSeedsTranscription FactorsAflatoxinsFungal ProteinsHistonesTranscription FactorsAcetylationAflatoxinHyphal fusionKojic acidSclerotia

Identifiers

PMID30130575
PMCPMC6215504

What OpenQuestion holds

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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.