Abstract
In mammalian cells, the Ku heterodimer is involved in DNA double-strand-break recognition and repair. We have established in yeast a connection between Ku activity and DNA double-strand-break damage repair, and a connection between Ku activity and commitment to DNA replication. We generated double-stranded DNA breaks in yeast cells in vivo by expressing a restriction endonuclease and have shown that yeast mutants lacking Ku p70 activity died while isogenic wild-type cells did not. Moreover, we have discovered that DNA damage occurs spontaneously during normal yeast mitotic growth, and that Ku functions in repair of this damage. We also observed that mitotically growing Ku p70 mutants have an anomalously high DNA content, suggesting a role for Ku in regulation of DNA synthesis. Finally, we present evidence that Ku p70 function is conserved between yeast, Drosophila, and humans.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Antigens, Nuclear*
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Cell Cycle / physiology*
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Cell Cycle Proteins*
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DNA Damage
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DNA Helicases*
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DNA Repair / physiology*
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DNA Replication / physiology*
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DNA, Fungal / biosynthesis
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DNA, Fungal / genetics
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / physiology*
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Drosophila melanogaster
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Fungal Proteins / genetics
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Fungal Proteins / physiology
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Genetic Complementation Test
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Humans
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Ku Autoantigen
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Mating Factor
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Mutation
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Nuclear Proteins / genetics
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Nuclear Proteins / physiology*
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Peptides / pharmacology
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Phenotype
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Saccharomyces cerevisiae / genetics*
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Saccharomyces cerevisiae Proteins*
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Temperature
Substances
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Antigens, Nuclear
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Cell Cycle Proteins
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DNA, Fungal
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DNA-Binding Proteins
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Fungal Proteins
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Nuclear Proteins
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Peptides
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Saccharomyces cerevisiae Proteins
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high affinity DNA-binding factor, S cerevisiae
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rad9 protein
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Mating Factor
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DNA Helicases
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XRCC5 protein, human
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Xrcc6 protein, human
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Ku Autoantigen