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Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication
Open accessAbstract
Defects in mitochondrial oxidative phosphorylation have frequently been associated with Alzheimer's disease (AD), and both inherited and somatic mtDNA mutations have been reported in certain AD cases. To determine whether mtDNA mutations contribute more generally to the etiology of AD, we have investigated the sequence of the mtDNA control region (CR) from AD brains for possible disease-causing mutations. Sixty-five percent of the AD brains harbored the T414G mutation, whereas this mutation was absent from all controls. Moreover, cloning and sequencing of the mtDNA CR from patient and control brains revealed that all AD brains had an average 63% increase in heteroplasmic mtDNA CR mutations and that AD brains from patients 80 years and older had a 130% increase in heteroplasmic CR mutations. In addition, these mutations preferentially altered known mtDNA regulatory elements. Certain AD brains harbored the disease-specific CR mutations T414C and T477C, and several AD brains between 74 and 83 years of age harbored the CR mutations T477C, T146C, and T195C, at levels up to 70-80% heteroplasmy. AD patient brains also had an average 50% reduction in the mtDNA L-strand ND6 transcript and in the mtDNA/nuclear DNA ratio. Because reduced ND6 mRNA and mtDNA copy numbers would reduce brain oxidative phosphorylation, these CR mutations could account for some of the mitochondrial defects observed in AD.
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“which has been described in an AD brain [169,170] in which base deletions correlate with complex IV deficiency in an AD hippocampus [171].”
From Mitochondrial Oxidative and Nitrosative Stress and Alzheimer Disease (2020) · cites this paper as [170]
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Citations
Cites
The genetical theory of natural selection
Fisher, R. A. (1930) · doi:10.5962/bhl.title.27468 · Cited by 17,617
Natural Selection of Parental Ability to Vary the Sex Ratio of Offspring
Trivers, R. L., & Willard, D. E. (1973) · Science · doi:10.1126/science.179.4068.90 · Cited by 3,822
Hamilton, W. D. O. (1967) · Science · doi:10.1126/science.156.3774.477 · Cited by 3,605
Charnov, E. L. (1982) · PubMed · Cited by 2,886
Identification Guide to European Passerines
Sevensson, L. (1975) · Medical Entomology and Zoology · Cited by 2,561
ABAD Directly Links Aß to Mitochondrial Toxicity in Alzheimer's Disease
Lustbader, J. W., Cirilli, M., Lin, C., Xu, H. W., Takuma, K., Wang, N., Caspersen, C., Chen, X., Pollak, S., Chaney, M., et al. (2004) · Science · doi:10.1126/science.1091230 · Cited by 1,303
Huang, X., Atwood, C., Hartshorn, M. A., Multhaup, G., Goldstein, L. E., Scarpa, R. C., Cuajungco, M. P., Gray, D. N., Lim, J. T., Moir, R. D., et al. (1999) · Biochemistry · doi:10.1021/bi990438f · Cited by 1,117
MITOCHONDRIAL DNA MAINTENANCE IN VERTEBRATES
Shadel, G. S., & Clayton, D. A. (1997) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.66.1.409 · Cited by 1,059
Tracing European Founder Lineages in the Near Eastern mtDNA Pool
Richards, M. B., Macaulay, V. A., Hickey, E., Vega, E., Sykes, B. C., Guida, V., Rengo, C., Sellitto, D., Cruciani, F., Kivisild, T., et al. (2000) · The American Journal of Human Genetics · doi:10.1016/s0002-9297(07)62954-1 · Cited by 952
Sex Ratio and Local Resource Competition in a Prosimian Primate
Clark, A. B. (1978) · Science · doi:10.1126/science.201.4351.163 · Cited by 910
Research works printed but not linked: 1
- Gibson, G. E. & Huang, H. M. (2002) Front. Biosci. 7, d1007-d1015.11897553
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Croock, D. A., Swart, Y., Sanko, T. J., Mavumengwana, V., Möller, M., Uren, C., & Petersen, D. C. (2025) · Tuberculosis · doi:10.1016/j.tube.2025.102650 · Cited by 4
Sharma, Y., Gupta, J. K., Babu, M. A., Singh, S., & Sindhu, R. K. (2024) · Journal of Molecular Neuroscience · doi:10.1007/s12031-024-02269-5 · Cited by 6
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Rodríguez‐Santiago, B., & Nunes, V. (2004) · Neurobiology of Disease · doi:10.1016/j.nbd.2004.10.004 · Cited by 4
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Wallace, D. C. (2010) · Wiley eBooks · doi:10.1002/9781444327335.ch2 · Cited by 3
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Francione, L. M., & Fisher, P. R. (2010) · Current Chemical Biology · doi:10.2174/2212796811004010032 · Cited by 3
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Wilkins, H. M., Weidling, I., Koppel, S., Wang, X., von Schulze, A., & Swerdlow, R. H. (2018) · The Molecular and Cellular Basis of Neurodegenerative Diseases · doi:10.1016/b978-0-12-811304-2.00013-4 · Cited by 2
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Xu, M., Li, T., Liu, X., Islam, B., Xiang, Y., Zou, X., & Wang, J. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04311-9 · Cited by 2
Kabelíková, P., Ivovič, D., Sumbalová, Z., Karhánek, M., TATAYOVA, L., Škopková, M., Cagalinec, M., Bruderová, V., Roška, J., & Jurkovičová, D. (2024) · Cancer Drug Resistance · doi:10.20517/cdr.2024.141 · Cited by 2
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Fu, T., Chen, X., Zhang, S., Fu, Y., Huang, L., & Xiong, W. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-25-00495 · Cited by 1
de Miranda, A. S., Vieira, É. L. M., Teixeira, A. L., & Bauer, M. E. (2026) · NeuroImmunoModulation · doi:10.1159/000550781 · Cited by 1
Shi, N., & Li, X. (2026) · Frontiers in Aging · doi:10.3389/fragi.2026.1830839 · Cited by 1
Mitochondrial DNA in neurons and its modulation by neurotoxins
Santos, M. S. (2006) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1
Mitochondrial Dysfunction in Stem Cell Aging
Meiliana, A., Dewi, N. M., & Wijaya, A. (2015) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v7i1.18 · Cited by 1
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Niemi, A. (2005) · Cited by 1
Perna, S., Bologna, C., Cavagna, P., Bernardinelli, L., Guido, D., Peroni, G., & Rondanelli, M. (2016) · Genetika · doi:10.2298/gensr1602515p · Cited by 1
Mitochondrial DNA mutations in gynecological cancers
Księżakowska‐Łakoma, K., Nowińska-Serwach, A., & Wilczyński, J. R. (2011) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 1
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Farooqui, A. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809937-7.00004-5 · Cited by 1
Mitochondrial abnormalities in neurological disorders
Ferreira, A. F. F., Singulani, M. P., & de Britto, L. R. G. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822416-8.00012-9 · Cited by 1
Kamfar, S., Danaei, B., Rahimi, S., & Zeinali, V. (2024) · Mitochondrion · doi:10.1016/j.mito.2024.101888 · Cited by 1
Golden, T. R., Morten, K., Johnson, F., Samper, E., & Melov, S. (2005) · Elsevier eBooks · doi:10.1016/b978-012088387-5/50008-x · Cited by 1
Coenzyme Q, mtDNA and Mitochondrial Dysfunction During Aging
Quiles, J. L., Varela‐López, A., Navarro‐Hortal, M. D., & Battino, M. A. (2020) · Springer eBooks · doi:10.1007/978-3-030-45642-9_10 · Cited by 1
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Ganguly, B. B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90456-8.00001-6 · Cited by 1
Wallace, D. C. (2005) · Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics · doi:10.1002/047001153x.g105317 · Cited by 1
Role of Environmental and Inflammatory Toxicity in Neuronal Cell Death
Somayajulu‐Nitu, M., Domazet-Damjanov, D., Matei, A., Schwartzenberger, E., Cohen, J. S., & Pandey, S. (2008) · The Open Toxicology Journal · doi:10.2174/1874340400802010026 · Cited by 1
Dechant, J. J. (2013) · D-Scholarship@Pitt (University of Pittsburgh)
Mitochondrial Involvement in Neurodegeneration and Aging
Pickrell, A. M. (2012)
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Ortiz, G. G., Pacheco-Moisés, F. P., García-Trejo, J. D. J., Rocio, E., Miguel, A., Jose, A., Irma, E., Arias‐Merino, E. D., & de la Ros, A. C. (2011) · InTech eBooks · doi:10.5772/16713
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Metadata
- Authors
- Coskun, P. E., Beal, M. F., & Wallace, D. C.
- Affiliations
- University of California, Irvine (US)
- Corresponding author
- Wallace, Douglas C.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2004-07-09
- Volume
- 101
- Issue
- 29
- Pages
- 10726-10731
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC490002
- OpenAlex
- W2126773395
- Cited by
- 556
- References
- 89
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 14 · 2023: 18 · 2022: 35 · 2021: 38 · 2020: 28 · 2019: 25 · 2018: 18 · 2017: 16 · 2016: 23 · 2015: 15 · 2014: 19 · 2013: 30 · 2012: 24
- FWCI
- 11.29
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ellison Medical Foundation
- Emory University
- National Institutes of Health
- University of California, Irvine
- National Institute on Aging (R01AG020729, AG-13154, AG 20729, R01AG013154)
- National Institute of Neurological Disorders and Stroke (NS-21328, R01NS021328)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- Alzheimer's disease, mitochondrial DNA, mitochondrial DNA control region, somatic mutations, heteroplasmy, mitochondrial transcription, mitochondrial DNA replication, oxidative phosphorylation, mitochondrial DNA copy number, brain aging
- MeSH terms
- Aged, Aged, 80 and over, Alzheimer Disease, Brain, DNA Mutational Analysis, DNA Replication, DNA, Mitochondrial, Humans, Mutation, Oxidative Phosphorylation, Transcription, Genetic, Locus Control Region
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