Mitochondrial DNA sequence variation in human evolution and disease - PubMed (original) (raw)
Review
Mitochondrial DNA sequence variation in human evolution and disease
D C Wallace. Proc Natl Acad Sci U S A. 1994.
Abstract
Germ-line and somatic mtDNA mutations are hypothesized to act together to shape our history and our health. Germ-line mtDNA mutations, both ancient and recent, have been associated with a variety of degenerative diseases. Mildly to moderately deleterious germ-line mutations, like neutral polymorphisms, have become established in the distant past through genetic drift but now may predispose certain individuals to late-onset degenerative diseases. As an example, a homoplasmic, Caucasian, tRNA(Gln) mutation at nucleotide pair (np) 4336 has been observed in 5% of Alzheimer disease and Parkinson disease patients and may contribute to the multifactorial etiology of these diseases. Moderately to severely deleterious germ-line mutations, on the other hand, appear repeatedly but are eliminated by selection. Hence, all extant mutations of this class are recent and associated with more devastating diseases of young adults and children. Representative of these mutations is a heteroplasmic mutation in MTND6 at np 14459 whose clinical presentations range from adult-onset blindness to pediatric dystonia and basal ganglial degeneration. To the inherited mutations are added somatic mtDNA mutations which accumulate in random arrays within stable tissues. These mutations provide a molecular clock that measures our age and may cause a progressive decline in tissue energy output that could precipitate the onset of degenerative diseases in individuals harboring inherited deleterious mutations.
Similar articles
- Mitochondrial DNA mutations in diseases of energy metabolism.
Wallace DC. Wallace DC. J Bioenerg Biomembr. 1994 Jun;26(3):241-50. doi: 10.1007/BF00763096. J Bioenerg Biomembr. 1994. PMID: 8077179 Review. - Mitochondrial DNA mutations in human degenerative diseases and aging.
Wallace DC, Shoffner JM, Trounce I, Brown MD, Ballinger SW, Corral-Debrinski M, Horton T, Jun AS, Lott MT. Wallace DC, et al. Biochim Biophys Acta. 1995 May 24;1271(1):141-51. doi: 10.1016/0925-4439(95)00021-u. Biochim Biophys Acta. 1995. PMID: 7599200 Review. - Mitochondrial DNA mutations associated with aging and degenerative diseases.
Ozawa T. Ozawa T. Exp Gerontol. 1995 May-Aug;30(3-4):269-90. doi: 10.1016/0531-5565(94)00057-a. Exp Gerontol. 1995. PMID: 7556507 Review. - Mechanism of somatic mitochondrial DNA mutations associated with age and diseases.
Ozawa T. Ozawa T. Biochim Biophys Acta. 1995 May 24;1271(1):177-89. doi: 10.1016/0925-4439(95)00026-z. Biochim Biophys Acta. 1995. PMID: 7599206 Review. - Mitochondrial DNA mutations and oxidative damage in aging and diseases: an emerging paradigm of gerontology and medicine.
Wei YH. Wei YH. Proc Natl Sci Counc Repub China B. 1998 Apr;22(2):55-67. Proc Natl Sci Counc Repub China B. 1998. PMID: 9615468 Review.
Cited by
- A comparative analysis of chloroplast genomes revealed the chloroplast heteroplasmy of Artemisia annua.
Ding X, Pan H, Shi P, Zhao S, Bao S, Zhong S, Dai C, Chen J, Gong L, Zhang D, Qiu X, Liao B, Huang Z. Ding X, et al. Front Pharmacol. 2024 Aug 14;15:1466578. doi: 10.3389/fphar.2024.1466578. eCollection 2024. Front Pharmacol. 2024. PMID: 39206258 Free PMC article. - Precision mitochondrial medicine.
Chinnery PF. Chinnery PF. Camb Prism Precis Med. 2022 Nov 15;1:e6. doi: 10.1017/pcm.2022.8. eCollection 2023. Camb Prism Precis Med. 2022. PMID: 38550943 Free PMC article. Review. - Increased Diabetes Complications in a Mouse Model of Oxidative Stress Due to 'Mismatched' Mitochondrial DNA.
Januszewski AS, Blake R, Zhang M, Ma B, Anand S, Pinkert CA, Kelly DJ, Jenkins AJ, Trounce IA. Januszewski AS, et al. Antioxidants (Basel). 2024 Feb 1;13(2):187. doi: 10.3390/antiox13020187. Antioxidants (Basel). 2024. PMID: 38397785 Free PMC article. - Deciphering cell states and genealogies of human haematopoiesis.
Weng C, Yu F, Yang D, Poeschla M, Liggett LA, Jones MG, Qiu X, Wahlster L, Caulier A, Hussmann JA, Schnell A, Yost KE, Koblan LW, Martin-Rufino JD, Min J, Hammond A, Ssozi D, Bueno R, Mallidi H, Kreso A, Escabi J, Rideout WM 3rd, Jacks T, Hormoz S, van Galen P, Weissman JS, Sankaran VG. Weng C, et al. Nature. 2024 Mar;627(8003):389-398. doi: 10.1038/s41586-024-07066-z. Epub 2024 Jan 22. Nature. 2024. PMID: 38253266 Free PMC article. - New insights on mitochondrial heteroplasmy observed in ovarian diseases.
Zhou Y, Jin Y, Wu T, Wang Y, Dong Y, Chen P, Hu C, Pan N, Ye C, Shen L, Lin M, Fang T, Wu R. Zhou Y, et al. J Adv Res. 2024 Nov;65:211-226. doi: 10.1016/j.jare.2023.11.033. Epub 2023 Dec 6. J Adv Res. 2024. PMID: 38061426 Free PMC article. Review.
References
- Am J Hum Genet. 1993 Sep;53(3):563-90 - PubMed
- Am J Hum Genet. 1993 Sep;53(3):591-608 - PubMed
- Nat Genet. 1993 Jul;4(3):284-8 - PubMed
- Nat Genet. 1993 Jul;4(3):289-94 - PubMed
- Hum Genet. 1993 Oct;92(4):379-84 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous