» Articles » PMID: 32989265

Extreme Heterogeneity of Human Mitochondrial DNA from Organelles to Populations

Overview
Journal Nat Rev Genet
Specialty Genetics
Date 2020 Sep 29
PMID 32989265
Citations 96
Authors
Affiliations
Soon will be listed here.
Abstract

Contrary to the long-held view that most humans harbour only identical mitochondrial genomes, deep resequencing has uncovered unanticipated extreme genetic variation within mitochondrial DNA (mtDNA). Most, if not all, humans contain multiple mtDNA genotypes (heteroplasmy); specific patterns of variants accumulate in different tissues, including cancers, over time; and some variants are preferentially passed down or suppressed in the maternal germ line. These findings cast light on the origin and spread of mtDNA mutations at multiple scales, from the organelle to the human population, and challenge the conventional view that high percentages of a mutation are required before a new variant has functional consequences.

Citing Articles

Aging-associated accumulation of mitochondrial DNA mutations in tumor origin.

Kong M, Guo L, Xu W, He C, Jia X, Zhao Z Life Med. 2025; 1(2):149-167.

PMID: 39871923 PMC: 11749795. DOI: 10.1093/lifemedi/lnac014.


Mitochondrial diseases: from molecular mechanisms to therapeutic advances.

Wen H, Deng H, Li B, Chen J, Zhu J, Zhang X Signal Transduct Target Ther. 2025; 10(1):9.

PMID: 39788934 PMC: 11724432. DOI: 10.1038/s41392-024-02044-3.


Aging through the lens of mitochondrial DNA mutations and inheritance paradoxes.

Chen J, Li H, Liang R, Huang Y, Tang Q Biogerontology. 2024; 26(1):33.

PMID: 39729246 DOI: 10.1007/s10522-024-10175-x.


Mitochondrial tRNA modifications: functions, diseases caused by their loss, and treatment strategies.

Chujo T, Tomizawa K RNA. 2024; 31(3):382-394.

PMID: 39719325 PMC: 11874988. DOI: 10.1261/rna.080257.124.


Preventing excessive autophagy protects from the pathology of mtDNA mutations in Drosophila melanogaster.

El Fissi N, Rosenberger F, Chang K, Wilhalm A, Barton-Owen T, Hansen F Nat Commun. 2024; 15(1):10719.

PMID: 39715749 PMC: 11666730. DOI: 10.1038/s41467-024-55559-2.


References
1.
Anderson S, Bankier A, Barrell B, de Bruijn M, Coulson A, Drouin J . Sequence and organization of the human mitochondrial genome. Nature. 1981; 290(5806):457-65. DOI: 10.1038/290457a0. View

2.
Holt I, Harding A, Morgan-Hughes J . Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature. 1988; 331(6158):717-9. DOI: 10.1038/331717a0. View

3.
Boulet L, Karpati G, Shoubridge E . Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF). Am J Hum Genet. 1992; 51(6):1187-200. PMC: 1682926. View

4.
Gorman G, Schaefer A, Ng Y, Gomez N, Blakely E, Alston C . Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease. Ann Neurol. 2015; 77(5):753-9. PMC: 4737121. DOI: 10.1002/ana.24362. View

5.
Bendall K, Macaulay V, Baker J, Sykes B . Heteroplasmic point mutations in the human mtDNA control region. Am J Hum Genet. 1996; 59(6):1276-87. PMC: 1914856. View