Cited by 89Evolution and Genetic DynamicsFungal and yeast genetics researchDNA Repair Mechanisms

Ploidy controls the success of mutators and nature of mutations during budding yeast evolution

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Thompson, Dawn A., Desai, Michael M., Murray, Andrew W.·2006·Current Biology

Abstract

Background We used the budding yeast Saccharomyces cerevisiae to ask how elevated mutation rates affect the evolution of asexual eukaryotic populations. Mismatch repair defective and nonmutator strains were competed during adaptation to four laboratory environments (rich medium, low glucose, high salt, and a nonfermentable carbon source).Results In diploids, mutators have an advantage over nonmutators in all conditions, and mutators that win competitions are on average fitter than nonmutator winners. In contrast, haploid mutators have no advantage when competed against haploid nonmutators, and haploid mutator winners are less fit than nonmutator winners. The diploid mutator winners were all superior to their ancestors both in the condition they had adapted to, and in two of the other conditions. This phenotype was due to a mutation or class of mutations that confers a large growth advantage during the respiratory phase of yeast cultures that precedes stationary phase. This generalist mutation(s) was not selected in diploid nonmutator strains or in haploid strains, which adapt primarily by fixing specialist (condition-specific) mutations. In diploid mutators, such mutations also occur, and the majority accumulates after the fixation of the generalist mutation.Conclusions We conclude that the advantage of mutators depends on ploidy and that diploid mutators can give rise to beneficial mutations that are inaccessible to nonmutators and haploid mutators.

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Crossref · 10.1016/j.cub.2006.06.070

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  • Mutations can be more readily assimilated in a diploid than in a haploid organism, since deleterious mutations are potentially buffered by a functional version.

    “Mutations can be more readily assimilated in a diploid than in a haploid organism, since deleterious mutations are potentially buffered by a functional version (Thompson et al., 2006).”

    From The evolution of drug resistance in clinical isolates of Candida albicans. (2015) · cites this paper as Thompson et al., 2006

  • Past work in S. cerevisiae suggests that diploids adapt more quickly in msh2 mutant backgrounds, rather than less, suggesting that ploidy may play the opposite role, at least in S. cerevisiae.

    “However, past work in S. cerevisiae suggests that diploids adapt more quickly in msh2 mutant backgrounds, rather than less, suggesting that ploidy may play the opposite role, at least in S. cerevisiae (Thompson et al., 2006).”

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References 41 · Cited by 89

Authors
Thompson, D. A., Desai, M. M., & Murray, A. W.
Affiliations
Harvard University (US)
Corresponding author
Murray, Andrew W.
Venue
Current Biology
Publisher
Elsevier BV
Published
2006-08
Volume
16
Issue
16
Pages
1581-1590
ISSN
0960-9822 (ISSN-L)
OpenAlex
W2113430775
Cited by
89
References
41
Citations by year
2025: 2 · 2023: 4 · 2022: 5 · 2021: 2 · 2020: 5 · 2019: 3 · 2018: 4 · 2017: 10 · 2016: 5 · 2015: 7 · 2014: 6 · 2013: 6 · 2012: 5
FWCI
2.27
Type
journal article
Language
en
Open access
Locations
  • Current Biology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01gm055840-07)
  • National Cancer Institute (CA96470, P20CA096470)
  • National Institute of General Medical Sciences (P50GM068763, GM 55840)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
Keywords
mutation rate, mutators, ploidy, Saccharomyces cerevisiae, DNA mismatch repair, diploids, haploid plants, competition (biology), adaptation, fitness, respiratory growth, stationary phase
MeSH terms
Adaptation, Physiological, Flow Cytometry, Mutation, Ploidies, Saccharomyces cerevisiae, Evolution, Molecular

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