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Mitochondrial DNA mutations in human degenerative diseases and aging.
- 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.
- Subjects :
- Adult
Aged
Amino Acid Sequence
Animals
Child
Conserved Sequence
Energy Metabolism
Female
Humans
Male
Middle Aged
Mitochondrial Myopathies metabolism
Molecular Sequence Data
Nervous System Diseases genetics
Nervous System Diseases metabolism
Optic Atrophies, Hereditary metabolism
Oxidative Phosphorylation
Pedigree
Sequence Homology, Amino Acid
Aging genetics
Biological Evolution
DNA, Mitochondrial genetics
Mitochondria metabolism
Mitochondrial Myopathies genetics
Mutation
Optic Atrophies, Hereditary genetics
Point Mutation
Subjects
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