Literature DB >> 8428629

The point mutation of mitochondrial DNA characteristic for MERRF disease is found also in healthy people of different ages.

C Münscher1, T Rieger, J Müller-Höcker, B Kadenbach.   

Abstract

The A-to-G transition mutation in the tRNA(Lys) gene of mitochondrial DNA (mtDNA), characteristic for the maternally inherited MERRF syndrome (myoclonic epilepsy with ragged red fibers), has been identified by point mutation-specific polymerase chain reaction in extraocular muscle from 11 of 16 healthy people of different ages. No mutation was found in navel-string samples from 5 newborns, in HeLa cells, and in 2 individuals younger than 20 years. On the other hand, the mutation is present in all 5 tested 74-89-year-old individuals and in 6 of 9 20-70-year-old individuals. The amount of mutated from total mtDNA was estimated by 'mispairing PCR' in extraocular muscle of 2 individuals of 74 and 89 years to 2.0 and 2.4%, respectively. In most tissue samples the MERRF mutation occurs together with the 'common deletion' of mtDNA, which was previously shown to accumulate in healthy individuals with increasing age. It is proposed that during aging, deletions and point mutations of mtDNA accumulate, which could impair mitochondrial energetics.

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Year:  1993        PMID: 8428629     DOI: 10.1016/0014-5793(93)81484-h

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  21 in total

1.  The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method.

Authors:  D G Murdock; N C Christacos; D C Wallace
Journal:  Nucleic Acids Res       Date:  2000-11-01       Impact factor: 16.971

2.  Human brain contains high levels of heteroplasmy in the noncoding regions of mitochondrial DNA.

Authors:  E E Jazin; L Cavelier; I Eriksson; L Oreland; U Gyllensten
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-29       Impact factor: 11.205

Review 3.  Mitochondrial DNA repair in aging and disease.

Authors:  Nadiya M Druzhyna; Glenn L Wilson; Susan P LeDoux
Journal:  Mech Ageing Dev       Date:  2008-03-13       Impact factor: 5.432

4.  Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging.

Authors:  F Pallotti; X Chen; E Bonilla; E A Schon
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

5.  Mitochondrial mutational spectra in human cells and tissues.

Authors:  K Khrapko; H A Coller; P C André; X C Li; J S Hanekamp; W G Thilly
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-09       Impact factor: 11.205

Review 6.  Mitochondrial involvement in the ageing process. Facts and controversies.

Authors:  E J Brierley; M A Johnson; O F James; D M Turnbull
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

7.  Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells.

Authors:  I Trounce; J Schmiedel; H C Yen; S Hosseini; M D Brown; J J Olson; D C Wallace
Journal:  Nucleic Acids Res       Date:  2000-05-15       Impact factor: 16.971

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

Review 9.  Mitochondrial DNA sequence variation in human evolution and disease.

Authors:  D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

10.  The unusual structures of the hot-regions flanking large-scale deletions in human mitochondrial DNA.

Authors:  J H Hou; Y H Wei
Journal:  Biochem J       Date:  1996-09-15       Impact factor: 3.857

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