Abstract
The importance of mitochondrial DNA (mtDNA) deletions in the progeroid phenotype of exonuclease-deficient DNA polymerase γ mice has been intensely debated. We show that disruption of Mip1 exonuclease activity increases mtDNA deletions 160-fold, whereas disease-associated polymerase variants were mostly unaffected, suggesting that exonuclease activity is vital to avoid deletions during mtDNA replication.
Keywords:
Mip1; Pol Gamma; direct repeats; exonuclease; mtDNA deletions.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, N.I.H., Intramural
MeSH terms
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DNA Polymerase I / genetics
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DNA Polymerase I / metabolism*
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DNA, Fungal / analysis
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DNA, Mitochondrial / analysis*
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Microsatellite Repeats / genetics*
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Mitochondria / enzymology*
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Mitochondria / genetics
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Saccharomyces cerevisiae / enzymology
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Saccharomyces cerevisiae / genetics
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Saccharomyces cerevisiae / metabolism*
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Saccharomyces cerevisiae Proteins / genetics
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Saccharomyces cerevisiae Proteins / metabolism*
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Sequence Deletion*
Substances
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DNA, Fungal
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DNA, Mitochondrial
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Saccharomyces cerevisiae Proteins
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DNA Polymerase I
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MIP1 protein, S cerevisiae