Literature DB >> 7753635

Increased frequency of deletions in the mitochondrial genome with age of Caenorhabditis elegans.

S Melov1, G J Lithgow, D R Fischer, P M Tedesco, T E Johnson.   

Abstract

We have developed a long-extension-PCR strategy which amplifies approximately half of the mitochondrial genome (6.3 kb) of Caenorhabditis elegans using an individual worm as target. We analyzed three strains over their life span to assess the number of detectable deletions in the mitochondrial genome. Two of these strains are wild-type for life span while the third is mutant in the age-1 gene, approximately doubling its maximum life span. At the mean life span in wild-type strains, there was a significant difference between the frequency of deletions detected in the mitochondrial genome compared with the mean number of deletions in young animals. In addition, deletions in the mitochondrial genome occur at a significantly lower rate in age-1 mutants as compared with wild type. We cloned and identified the breakpoints of two deletions and found that one of the deletions had a direct repeat of 8 bp at the breakpoint. This is the largest single study (over 900 individual animals) characterizing the frequency of deletions in the mitochondrial genome as a function of age yet carried out.

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Year:  1995        PMID: 7753635      PMCID: PMC306871          DOI: 10.1093/nar/23.8.1419

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  36 in total

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Authors:  T E Johnson
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Authors:  L Pikó; A J Hougham; K J Bulpitt
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10.  Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

Authors:  S Mita; R Rizzuto; C T Moraes; S Shanske; E Arnaudo; G M Fabrizi; Y Koga; S DiMauro; E A Schon
Journal:  Nucleic Acids Res       Date:  1990-02-11       Impact factor: 16.971

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  32 in total

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7.  Cytosolic ribosomal mutations that abolish accumulation of circular intron in the mitochondria without preventing senescence of Podospora anserina.

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8.  Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle.

Authors:  S Melov; J M Shoffner; A Kaufman; D C Wallace
Journal:  Nucleic Acids Res       Date:  1995-10-25       Impact factor: 16.971

9.  Hydrogen sulfide is an endogenous regulator of aging in Caenorhabditis elegans.

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10.  Disruption of insulin signalling preserves bioenergetic competence of mitochondria in ageing Caenorhabditis elegans.

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