Journal
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
Volume 44, Issue 4, Pages 313-320Publisher
WILEY
DOI: 10.1002/em.20050
Keywords
rat; mitochondrial DNA; quantitative PCR; mitochondrial deletion; aging
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Funding
- NATIONAL CANCER INSTITUTE [R01CA041843] Funding Source: NIH RePORTER
- NCI NIH HHS [P30 CA41843] Funding Source: Medline
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Changes in mitochondrial DNA copy number and increases in mitochondrial DNA mutations, especially deletions, have been associated with exposure to mutagens and with aging. Common deletions that are the result of recombination between direct repeats in human and rat (4,977 and 4,834, bp, respectively) are known to increase in tissues of aged individuals. Previous studies have used long-distance PCR and Southern blot or quantitative PCR to determine the frequency of deleted mitochondrial DNA. A quantitative PCR (TaqMan) assay was developed to detect both mitochondrial DNA copy number and deletion frequency in the rat. This methodology allows not only the determination of changes in the amount of mitochondrial DNA deletion relative to total mitochondrial DNA but also to determine changes in total mitochondrial DNA relative to genomic DNA. As a validation of the assay in rat liver, the frequency of the common 4,834 bp deletion is shown to increase with age, while the relative mitochondrial DNA copy number rises at a young age (3-60 days), then decreases and holds fairly steady to 2 years of age. (C) 2004 Wiley-Liss, Inc.
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