Evidence map›Paper›PMID 40902103›Full record

ArticleG3 (Bethesda, Md.)2025

Genetic analysis of pigment production in the fungus Exophiala dermatitidis mutant strains obtained via nontargeted UV mutagenesis.

Kamaldeep Chhoker, Georg Hausner, Steven D Harris

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Clinical and Molecular Advances on the Black YeastInternational journal of molecular sciences · 2025
    Review
  2. Regulation of melanin production in fungi.Frontiers in fungal biology · 2025
    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

3 authors.

Kamaldeep ChhokerDepartment of Biological Sciences, University of Manitoba, Winnipeg, MB, Canada R3T 2N2.ORCID 0009-0004-4387-0177
Georg HausnerDepartment of Microbiology, University of Manitoba, Winnipeg, MB, Canada R3T 2N2.
Steven D HarrisDepartment of Biological Sciences, University of Manitoba, Winnipeg, MB, Canada R3T 2N2.ORCID 0000-0001-5196-1977

Funding

National Sciences and Engineering Research Council RGPIN-2018-05349
6 · The paper itself

Abstract

Exophiala dermatitidis is a polyextremotolerant black yeast species. E. dermatitidis produces 1,8-dihydroxynaphthalene (DHN) melanin via the polyketide synthase 1 (PKS1) pathway enabling it to survive harmful conditions. This study focused on random nontargeted mutagenesis to obtain albino (alb) and hyperpigmented (hyp) mutants. Notably, all 17 alb mutants possessed mutations in PKS1 whereas the 113 hyperpigmented (hyp) mutants harbored mutations impacting a range of functions. Cell morphology and phenotypic assays showed additional differences between the alb and hyp mutants. Strikingly, 3 of the albino mutants (alb1, alb2, and alb3) were conditional in that despite the presence of mutations in PKS1 they were able to produce melanin upon exposure to different carbon sources. These mutants otherwise shared similar cell morphology and growth patterns with the obligate albinos. No additional shared mutations were found among the conditional albinos. Temperature and UV irradiation assays demonstrated reduced growth of albino mutants at higher temperatures (i.e. 42 °C) and a greater sensitivity to higher doses of UV. Single nucleotide variant calling showed that some hyperpigmented mutants had a greater number of single nucleotide variants compared to albino strains. To date, this is the first study to generate and characterize conditional albino mutants in E. dermatitidis with the ability to recover melanin production.

Indexed as

ExophialaMutagenesisMutationPigments, BiologicalUltraviolet RaysFungal ProteinsMelaninsPhenotypePolyketide SynthasesFungal ProteinsMelaninsPigments, BiologicalPolyketide Synthases1-8albinoDHN melaninExophiala dermatitidishyperpigmentedphenotypic assayPKS1single nucleotide variants

Identifiers

PMID40902103
PMCPMC12693494

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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.