Abstract
We examined mismatch repair (MMR)-defective diploid strains of budding yeast grown for approximately 160 generations to determine whether decreases in spore viability due to the uncovering of recessive lethal mutations correlated with an increase in gross chromosomal rearrangements (GCRs). No GCRs were detected despite dramatic decreases in spore viability, suggesting that frameshift and/or other unrepaired DNA replication lesions play a greater role than chromosomal instability in decreasing viability in MMR-defective strains.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Adaptor Proteins, Signal Transducing
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Base Pair Mismatch / genetics*
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Cell Survival / genetics
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Chromosome Aberrations*
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Frameshift Mutation / physiology
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Fungal Proteins / genetics*
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Gene Rearrangement / physiology
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Genes, Lethal / physiology
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Genes, Recessive / physiology
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Models, Biological
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MutL Protein Homolog 1
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Mutation / physiology*
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Nucleic Acid Hybridization / methods
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Probability
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Saccharomyces cerevisiae / genetics*
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Saccharomyces cerevisiae Proteins
Substances
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Adaptor Proteins, Signal Transducing
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Fungal Proteins
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MLH1 protein, S cerevisiae
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Saccharomyces cerevisiae Proteins
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MutL Protein Homolog 1