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Mitochondrial DNA mutations in human degenerative diseases and aging.

Authors :
Wallace DC
Shoffner JM
Trounce I
Brown MD
Ballinger SW
Corral-Debrinski M
Horton T
Jun AS
Lott MT
Source :
Biochimica et biophysica acta [Biochim Biophys Acta] 1995 May 24; Vol. 1271 (1), pp. 141-51.
Publication Year :
1995

Abstract

A wide variety of mitochondrial DNA (mtDNA) mutations have recently been identified in degenerative diseases of the brain, heart, skeletal muscle, kidney and endocrine system. Generally, individuals inheriting these mitochondrial diseases are relatively normal in early life, develop symptoms during childhood, mid-life, or old age depending on the severity of the maternally-inherited mtDNA mutation; and then undergo a progressive decline. These novel features of mtDNA disease are proposed to be the product of the high dependence of the target organs on mitochondrial bioenergetics, and the cumulative oxidative phosphorylation (OXPHOS) defect caused by the inherited mtDNA mutation together with the age-related accumulation mtDNA mutations in post-mitotic tissues.

Details

Language :
English
ISSN :
0006-3002
Volume :
1271
Issue :
1
Database :
MEDLINE
Journal :
Biochimica et biophysica acta
Publication Type :
Academic Journal
Accession number :
7599200
Full Text :
https://doi.org/10.1016/0925-4439(95)00021-u