Abstract
Deletions of the mitochondrial DNA (mtDNA) have been shown to accumulate with age in a variety of species regardless of mean or maximal life span. This implies that such mutations are either a molecular biomarker of senescence or that they are more causally linked to senescence itself. One assay that can be used to detect these mtDNA mutations is the long-extension polymerase chain reaction assay. This assay amplifies ~16 kb of the mtDNA in mammalian mitochondria and preferentially amplifies mtDNAs that are either deleted or duplicated. We have applied this assay to the aging human brain and found a heterogeneous array of rearranged mtDNAs. In addition, we have developed in situ polymerase chain reaction to detect mtDNA within individual cells of both the mouse and the human brain as a first step in identifying and enumerating cells containing mutant mtDNAs in situ. Copyright (C) 1999 Elsevier Science Inc.
| Original language | English |
|---|---|
| Pages (from-to) | 565-571 |
| Number of pages | 7 |
| Journal | Neurobiology of Aging |
| Volume | 20 |
| Issue number | 5 |
| DOIs | |
| State | Published - Sep 1999 |
Keywords
- ANT1
- Adenine nucleotide translocator
- Aging
- Deletions
- Energy
- Human brain
- In situ PCR
- Mitochondria
- Mitochondrial DNA mutations
- Mouse
- Oxidative stress
- Superoxide
- Superoxide dismutase
- mtDNA
ASJC Scopus subject areas
- General Neuroscience
- Aging
- Developmental Biology
- Clinical Neurology
- Geriatrics and Gerontology
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