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A modified fluctuation assay reveals a natural mutator phenotype that drives mutation spectrum variation within Saccharomyces cerevisiae

View ORCID ProfilePengyao Jiang, View ORCID ProfileAnja R. Ollodart, Vidha Sudhesh, View ORCID ProfileAlan J. Herr, View ORCID ProfileMaitreya J. Dunham, View ORCID ProfileKelley Harris
doi: https://doi.org/10.1101/2021.01.11.425955
Pengyao Jiang
1Department of Genome Sciences, University of Washington, Seattle, WA
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Anja R. Ollodart
1Department of Genome Sciences, University of Washington, Seattle, WA
2Molecular and Cellular Biology Program, University of Washington, Seattle, WA
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Vidha Sudhesh
1Department of Genome Sciences, University of Washington, Seattle, WA
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Alan J. Herr
3Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA
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Maitreya J. Dunham
1Department of Genome Sciences, University of Washington, Seattle, WA
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Kelley Harris
1Department of Genome Sciences, University of Washington, Seattle, WA
4Department of Computational Biology, Fred Hutchinson Cancer Research Center, Seattle, WA
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  • For correspondence: harriske@uw.edu
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Abstract

Mutations are the source of genetic variation and a prerequisite for evolution. Despite their fundamental importance, however, their rarity makes them expensive and difficult to detect, which has limited our ability to measure the extent to which mutational processes vary within and between species. Here, we use the 1011 Saccharomyces cerevisiae collection to measure variation of mutation rates and spectra among strains isolated from a variety of natural and human-related environments. The mutation spectra of variants segregating in different S. cerevisiae populations exhibit differences in the relative numbers of specific transition and transversion types, a pattern reminiscent of previously observed mutation spectrum differences between populations of humans, great apes, and mice. Such natural variation is thought to reveal historical differences in the activity of particular mutational processes, but is also potentially complicated by other forces such as admixture, genetic drift, and selection. In order to directly test how much of the observed mutation spectrum variation is caused by heritable differences between extant strains of S. cerevisiae, we developed an experimental pipeline to assay de novo mutation rates and spectra of individual strains, using the reporter gene CAN1. We found a 10-fold range of mutation rate variation among 16 haploid strains surveyed. While many strains exhibit similar mutation spectra, two related strains from the panel’s “Mosaic beer” clade, known as AEQ and AAR, share a distinctive mutation spectrum enrichment for C>A mutations. This C>A enrichment found through our experimental pipeline mirrors an enrichment of C>A mutations in rare variants segregating throughout the genomes of AEQ and AAR as well as additional Mosaic beer strains. We deduce that a major axis of S. cerevisiae mutation spectrum variation is likely driven by one or more naturally occurring mutator alleles whose action is measurable in a controlled laboratory environment.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-ND 4.0 International license.
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Posted January 11, 2021.
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A modified fluctuation assay reveals a natural mutator phenotype that drives mutation spectrum variation within Saccharomyces cerevisiae
Pengyao Jiang, Anja R. Ollodart, Vidha Sudhesh, Alan J. Herr, Maitreya J. Dunham, Kelley Harris
bioRxiv 2021.01.11.425955; doi: https://doi.org/10.1101/2021.01.11.425955
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A modified fluctuation assay reveals a natural mutator phenotype that drives mutation spectrum variation within Saccharomyces cerevisiae
Pengyao Jiang, Anja R. Ollodart, Vidha Sudhesh, Alan J. Herr, Maitreya J. Dunham, Kelley Harris
bioRxiv 2021.01.11.425955; doi: https://doi.org/10.1101/2021.01.11.425955

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