Cited by 14Fungal Infections and StudiesFungal and yeast genetics researchEvolution and Genetic Dynamics

A spontaneous mutation in DNA polymerase POL3 during in vitro passaging causes a hypermutator phenotype in Cryptococcus species

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Boyce, Kylie J., Cao, Chengjun, Xue, Chaoyang, Idnurm, Alexander·2020·DNA Repair

Abstract

Passaging of microbes in vitro can lead to the selection of microevolved derivatives with differing properties to their original parent strains. One well characterised instance is the phenotypic differences observed between the series of strains derived from the type strain of the human pathogenic fungus Cryptococcus neoformans. A second case was reported in the close relative Cryptococcus deneoformans, in which a well-studied isolate ATCC 24067 (52D) altered its phenotypic characteristics after in vitro passaging in different laboratories. One of these derivatives, ATCC 24067A, has decreased virulence and also exhibits a hypermutator phenotype, in which the mutation rate is increased compared to wild type. In this study, the molecular basis behind the changes in the lineage of ATCC 24067 was determined by next-generation sequencing of the parent and passaged strain genomes. This analysis resulted in the identification of a point mutation that causes a D270G amino acid substitution within the exonuclease proofreading domain of the DNA polymerase delta subunit encoded by POL3. Complementation with POL3 confirmed that this mutation is responsible for the hypermutator phenotype of this strain. Regeneration of the mutation in C. neoformans, to eliminate the additional mutations present in the ATCC 24067A genetic background, demonstrated that the hypermutator phenotype of the pol3 D270G mutant causes rapid microevolution in vitro but does not result in decreased virulence. These findings indicate that mutator strains can emerge in these pathogenic fungi without conferring a fitness cost, but the subsequent rapid accumulation of mutations can be deleterious.

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Crossref · 10.1016/j.dnarep.2019.102751

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  • A mutation in the proofreading domain of POL3 was shown to confer the hypermutator phenotype.

    “a mutation in the proofreading domain of POL3 (encoding the catalytic subunit of DNA polymerase δ) was also shown to confer the hypermutator phenotype31.”
  • A subset of Cryptococcus isolates have been identified as hypermutator strains, which contain mutations in core genes in the DNA mismatch repair pathway, most notably MSH2.

    “a subset of Cryptococcus isolates have been identified as hypermutator strains30,31, which contain mutations in core genes in the DNA mismatch repair pathway, most notably MSH2 (refs30,32,33)”

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Authors
Boyce, K. J., Cao, C., Xue, C., & Idnurm, A.
Affiliations
  • RMIT University (AU)
  • Rutgers, The State University of New Jersey (US)
  • The University of Melbourne (AU)
Corresponding author
  • Boyce, Kylie J.
  • Idnurm, Alexander
Venue
DNA Repair
Publisher
Elsevier BV
Published
2020-02
Volume
86
Pages
102751
ISSN
  • 1568-7856 (ISSN-L)
  • 1568-7864
OpenAlex
W2990757339
Cited by
14
References
52
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2022: 4 · 2021: 3 · 2020: 3
FWCI
1.90
Type
journal article
Language
en
Open access
Locations
  • DNA repair (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • RMIT Research Repository (RMIT University Library) (submittedVersion)
  • Figshare (submittedVersion, cc-by)
  • Minerva Access (University of Melbourne) (submittedVersion)
Funders
Australian Research Council (FT130100146, LP170100548)
Topics
  • Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
Keywords
hypermutator phenotype, DNA polymerase delta, Cryptococcus neoformans, Cryptococcus deneoformans, microevolution, mutator strains, virulence, fungal genome sequencing, complementation
MeSH terms
Animals, Cryptococcosis, Cryptococcus neoformans, DNA Polymerase III, Fungal Proteins, Phenotype, Serial Passage, Point Mutation, Sequence Analysis, DNA, Amino Acid Substitution, Mice, High-Throughput Nucleotide Sequencing

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