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 approximately 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.
journal_name
Neurobiol Agingjournal_title
Neurobiology of agingauthors
Melov S,Schneider JA,Coskun PE,Bennett DA,Wallace DCdoi
10.1016/s0197-4580(99)00092-5subject
Has Abstractpub_date
1999-09-01 00:00:00pages
565-71issue
5eissn
0197-4580issn
1558-1497pii
S0197458099000925journal_volume
20pub_type
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journal_title:Neurobiology of aging
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journal_title:Neurobiology of aging
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journal_title:Neurobiology of aging
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