Evidence map›Paper›PMID 41474550›Full record

ArticleGenetics2026

Contrasting mutation patterns in haploid and diploid cells from two yeast species.

Kevin Bao, Rutuja Gupte, Neil Braker, Nathaniel P Sharp

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Kevin BaoDepartment of Genetics, University of Wisconsin-Madison, 425-G Henry Mall, Madison, WI 53706, United States.
Rutuja GupteDepartment of Genetics, University of Wisconsin-Madison, 425-G Henry Mall, Madison, WI 53706, United States.
Neil BrakerDepartment of Genetics, University of Wisconsin-Madison, 425-G Henry Mall, Madison, WI 53706, United States.
Nathaniel P SharpDepartment of Genetics, University of Wisconsin-Madison, 425-G Henry Mall, Madison, WI 53706, United States.ORCID 0000-0001-6016-083X

Funding

The evolutionary and genomic drivers of mutation spectraR35GM154954 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Nathaniel Sharp · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM154954NIH HHS R35GM154954
6 · The paper itself

Abstract

There is significant variation in the rate and spectrum of spontaneous mutations among taxa. How this variation is shaped by natural selection remains a subject of debate. The drift-barrier hypothesis proposes that selection generally favors lower mutation rates due to the risk of deleterious mutations but acts less effectively against weak mutator alleles in smaller populations, allowing the mutation rate to increase due to genetic drift. Given this model, we propose that mutation rates may also be elevated in cell types that appear rarely in a population, where DNA replication and repair processes are subject to selection less often. We can begin to test this prediction in yeast species, some of which can be grown in either a haploid or diploid cell state. Existing data on the budding yeast Saccharomyces cerevisiae support this prediction, with a higher mutation rate observed in haploids, which is the rare cell type in natural populations. However, this pattern could also appear if haploidy is inherently mutagenic, regardless of the dominant cell type. To test these alternatives, we conducted a mutation accumulation experiment with haploid and diploid cells of the fission yeast Schizosaccharomyces pombe, in which diploidy is the rare cell type. In this species, we found a higher mutation rate in diploids, consistent with our prediction. In both species, the spectrum of mutations is also influenced by ploidy state. Our findings suggest that limits to selection on mutation may be evident as variation within species.

Indexed as

DiploidyHaploidyMutationMutation RateSchizosaccharomycesMutation AccumulationSaccharomyces cerevisiaeSelection, Geneticloss of heterozygositymat2-102

Identifiers

PMID41474550
PMCPMC13017439

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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.