Evidence map›Paper›PMID 25681180›Full record

ArticleApplied and environmental microbiology2015

Disparate independent genetic events disrupt the secondary metabolism gene perA in certain symbiotic Epichloë species.

Daniel Berry, Johanna E Takach, Christopher L Schardl, Nikki D Charlton, Barry Scott, Carolyn A Young

Open access · bronzeAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
9.8field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. The Compatibility of theJournal of fungi (Basel, Switzerland) · 2026
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  3. Identification and Characterization of ThreeJournal of fungi (Basel, Switzerland) · 2025
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  5. Identification of ThreeJournal of fungi (Basel, Switzerland) · 2022
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  6. Article
  7. Dissection of the epoxyjanthitrem pathway inFrontiers in fungal biology · 2022
    Article
  8. Genetic Diversity of the Symbiotic FungusFrontiers in microbiology · 2021
    Article
  9. Article
  10. Novel Antifungal Activity ofMicroorganisms · 2020
    Article
  11. Review
  12. Efficient nonenzymatic cyclization and domain shuffling drive pyrrolopyrazine diversity from truncated variants of a fungal NRPS.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Article
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  17. Article
  18. Article
  19. 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

6 authors at 3 institutions in 2 countries.

Daniel BerryInstitute of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
Johanna E TakachThe Samuel Roberts Noble Foundation, Ardmore, Oklahoma, USA.
Christopher L SchardlDepartment of Plant Pathology, University of Kentucky, Lexington, Kentucky, USA.
Nikki D CharltonThe Samuel Roberts Noble Foundation, Ardmore, Oklahoma, USA.
Barry ScottInstitute of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
Carolyn A YoungThe Samuel Roberts Noble Foundation, Ardmore, Oklahoma, USA cayoung@noble.org.
Noble Research Institute · USMassey University · NZUniversity of Kentucky · US

Funding

ZEBRAFISH VISUAL FUNCTION RECOVERY FOLLOWING OPTIC NERVE DAMAGEP20RR016481 · NCRR · UNIVERSITY OF LOUISVILLE · PI BARTON, HAZEL A · 2001 to 2011
$34.8M
Geometry of gene cophylogenies as relates to genome evolution and speciationR01GM086888 · NIGMS · UNIVERSITY OF KENTUCKY · PI YOSHIDA, RURIKO · 2008 to 2012
$1.4M
NCRR NIH HHS 2 P20 RR-16481NCRR NIH HHS P20 RR016481NIGMS NIH HHS R01 GM086888NIGMS NIH HHS R01GM086888
6 · The paper itself

Abstract

Peramine is an insect-feeding deterrent produced by Epichloë species in symbiotic association with C3 grasses. The perA gene responsible for peramine synthesis encodes a two-module nonribosomal peptide synthetase. Alleles of perA are found in most Epichloë species; however, peramine is not produced by many perA-containing Epichloë isolates. The genetic basis of these peramine-negative chemotypes is often unknown. Using PCR and DNA sequencing, we analyzed the perA genes from 72 Epichloë isolates and identified causative mutations of perA null alleles. We found nonfunctional perA-ΔR* alleles, which contain a transposon-associated deletion of the perA region encoding the C-terminal reductase domain, are widespread within the Epichloë genus and represent a prevalent mutation found in nonhybrid species. Disparate phylogenies of adjacent A2 and T2 domains indicated that the deletion of the reductase domain (R*) likely occurred once and early in the evolution of the genus, and subsequently there have been several recombinations between those domains. A number of novel point, deletion, and insertion mutations responsible for abolishing peramine production in full-length perA alleles were also identified. The regions encoding the first and second adenylation domains (A1 and A2, respectively) were common sites for such mutations. Using this information, a method was developed to predict peramine chemotypes by combining PCR product size polymorphism analysis with sequencing of the perA adenylation domains.

Indexed as

MutationEpichloeFungal ProteinsHeterocyclic Compounds, 2-RingMolecular Sequence DataPeptide SynthasesPhylogenyPoaceaePolyaminesPolymerase Chain ReactionSecondary MetabolismSequence Analysis, DNASymbiosisFungal ProteinsHeterocyclic Compounds, 2-RingPeptide SynthasesperaminePolyamines

Identifiers

PMID25681180
PMCPMC4375322
OpenAlexW2127026827

What OpenQuestion holds

Textmetadata
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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.