Literature DB >> 1551433

Multiple mitochondrial DNA deletions in an elderly human individual.

C Zhang1, A Baumer, R J Maxwell, A W Linnane, P Nagley.   

Abstract

We have used the polymerase chain reaction (PCR) to study deletions in the mitochondrial DNA (mtDNA) of an elderly human individual. An extended set of PCR primers has been utilised to identify 10 mitochondrial DNA deletions in a 69-year-old female subject with no known mitochondrial disease. The particular deletions visualised as PCR products depended on the primer pairs used, such that the more distantly separated PCR primers enabled visualisation of larger deletions. Some deletions were common to the heart, brain and skeletal muscle, whereas others were apparently specific to individual tissues. DNA sequencing analysis of PCR products showed that short direct repeat sequences (5 to 13 bp) flanked all deletion breakpoints; in most cases one copy of the repeat was deleted. It is proposed that the accumulation of such multiple deletions is a general phenomenon during the ageing process.

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Year:  1992        PMID: 1551433     DOI: 10.1016/0014-5793(92)80321-7

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


  29 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.  Mitochondrial DNA deletion mutations are concomitant with ragged red regions of individual, aged muscle fibers: analysis by laser-capture microdissection.

Authors:  Z Cao; J Wanagat; S H McKiernan; J M Aiken
Journal:  Nucleic Acids Res       Date:  2001-11-01       Impact factor: 16.971

Review 3.  Beneficial effects of exercise on age-related mitochondrial dysfunction and oxidative stress in skeletal muscle.

Authors:  Anna-Maria Joseph; Peter J Adhihetty; Christiaan Leeuwenburgh
Journal:  J Physiol       Date:  2015-11-21       Impact factor: 5.182

4.  Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers.

Authors:  Entela Bua; Jody Johnson; Allen Herbst; Bridget Delong; Debbie McKenzie; Shahriar Salamat; Judd M Aiken
Journal:  Am J Hum Genet       Date:  2006-07-07       Impact factor: 11.025

5.  Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly.

Authors:  J Müller-Höcker; P Seibel; K Schneiderbanger; B Kadenbach
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

6.  Mutations in mitochondrial DNA accumulate differentially in three different human tissues during ageing.

Authors:  V W Liu; C Zhang; P Nagley
Journal:  Nucleic Acids Res       Date:  1998-03-01       Impact factor: 16.971

7.  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

8.  Mapping frequencies of endogenous oxidative damage and the kinetic response to oxidative stress in a region of rat mtDNA.

Authors:  W J Driggers; G P Holmquist; S P LeDoux; G L Wilson
Journal:  Nucleic Acids Res       Date:  1997-11-01       Impact factor: 16.971

9.  Mutational analysis of the human mitochondrial genome branches into the realm of bacterial genetics.

Authors:  N Howell
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

10.  The mutation rate of the human mtDNA deletion mtDNA4977.

Authors:  R Shenkar; W Navidi; S Tavaré; M H Dang; A Chomyn; G Attardi; G Cortopassi; N Arnheim
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

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