| Literature DB >> 23589460 |
Jeffrey D Stumpf1, William C Copeland.
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.Entities:
Keywords: Mip1; Pol Gamma; direct repeats; exonuclease; mtDNA deletions
Mesh:
Substances:
Year: 2013 PMID: 23589460 PMCID: PMC3664861 DOI: 10.1534/genetics.113.150920
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562