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Germline mitochondrial DNA mutations aggravate ageing and can impair brain development
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Ageing is due to an accumulation of various types of damage, and mitochondrial dysfunction has long been considered to be important in this process. There is substantial sequence variation in mammalian mitochondrial DNA (mtDNA), and the high mutation rate is counteracted by different mechanisms that decrease maternal transmission of mutated mtDNA. Despite these protective mechanisms, it is becoming increasingly clear that low-level mtDNA heteroplasmy is quite common and often inherited in humans. We designed a series of mouse mutants to investigate the extent to which inherited mtDNA mutations can contribute to ageing. Here we report that maternally transmitted mtDNA mutations can induce mild ageing phenotypes in mice with a wild-type nuclear genome. Furthermore, maternally transmitted mtDNA mutations lead to anticipation of reduced fertility in mice that are heterozygous for the mtDNA mutator allele (PolgA(wt/mut)) and aggravate premature ageing phenotypes in mtDNA mutator mice (PolgA(mut/mut)). Unexpectedly, a combination of maternally transmitted and somatic mtDNA mutations also leads to stochastic brain malformations. Our findings show that a pre-existing mutation load will not only allow somatic mutagenesis to create a critically high total mtDNA mutation load sooner but will also increase clonal expansion of mtDNA mutations to enhance the normally occurring mosaic respiratory chain deficiency in ageing tissues. Our findings suggest that maternally transmitted mtDNA mutations may have a similar role in aggravating aspects of normal human ageing.
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“These and other data in this section argue inheritance determines an individual's baseline mitochondrial function and durability, and maternal inheritance plays a greater role than paternal inheritance [30].”
From The Alzheimer’s disease mitochondrial cascade hypothesis: progress and perspectives (2014) · cites this paper as [30]
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Cites
Premature ageing in mice expressing defective mitochondrial DNA polymerase
Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J. N., Rovio, A. T., Bruder, C. E., Bohlooly-Y, M., Gidlöf, S., Oldfors, A., Wibom, R., et al. (2004) · Nature · doi:10.1038/nature02517 · Cited by 2,734
Self-citationMitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
Kujoth, G. C., Hiona, A., Pugh, T. D., Someya, S., Panzer, K., Wohlgemuth, S. E., Hofer, T., Seo, A. Y., Sullivan, R., Jobling, W. A., et al. (2005) · Science · doi:10.1126/science.1112125 · Cited by 2,165
Understanding the odd science of aging
Kirkwood, T. B. L. (2005) · Cell · doi:10.1016/j.cell.2005.01.027 · Cited by 1,984
Mitochondrial role in cell aging
Miquel, J., Economos, A. C., Fleming, J., & Johnson, J. E. (1980) · Experimental Gerontology · doi:10.1016/0531-5565(80)90010-8 · Cited by 948
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age
Corral-Debrinski, M., Horton, T., Lott, M. T., Shoffner, J. M., Flint Beal, M., & Wallace, D. C. (1992) · Nature Genetics · doi:10.1038/ng1292-324 · Cited by 890
Detection of a specific mitochondrial DNA deletion in tissues of older humans
Cortopassi, G. A., & Arnheim, N. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.23.6927 · Cited by 788
On the nature of the aging process
Szilard, L. (1959) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.45.1.30 · Cited by 651
Somatic Mitochondrial DNA Mutations in Mammalian Aging
Larsson, N. (2010) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060408-093701 · Cited by 561
Self-citationMitochondrial DNA mutations in human colonic crypt stem cells
Taylor, R. W., Barron, M. J., Borthwick, G. M., Gospel, A., Chinnery, P. F., Samuels, D. C., Taylor, G. A., Plusa, S. M., Needham, S. J., Greaves, L. C., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci19435 · Cited by 530
Strong Purifying Selection in Transmission of Mammalian Mitochondrial DNA
Stewart, J. B., Freyer, C., Elson, J. L., Wredenberg, A., Cansu, Z., Trifunović, A., & Larsson, N. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060010 · Cited by 525
Self-citation
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Research works printed but not linked: 1
- Müller-Höcker, J. Cytochrome-c-oxidase deficient cardiomyocytes in the human heart — an age-related phenomenon. Am. J. Pathol. 134, 1167–1173 (1989)
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Sorted by citations
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Friedman, J. R., & Nunnari, J. (2014) · Nature · doi:10.1038/nature12985 · Cited by 1,803
The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease
Stewart, J. B., & Chinnery, P. F. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3966 · Cited by 1,041
Self-citationMitochondrial and metabolic dysfunction in ageing and age-related diseases
Amorim, J. A., Coppotelli, G., Rolo, A. P., Palmeira, C. M., Ross, J. M., & Sinclair, D. A. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00626-7 · Cited by 990
Self-citationThe Alzheimer’s disease mitochondrial cascade hypothesis: progress and perspectives
Swerdlow, R. H., Burns, J. M., & Khan, S. M. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.09.010 · Cited by 786
History and progress of hypotheses and clinical trials for Alzheimer’s disease
Liu, P.-P., Xie, Y., Meng, X.-Y., & Kang, J.-S. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0063-8 · Cited by 723
Maintenance and Expression of Mammalian Mitochondrial DNA
Gustafsson, C. M., Falkenberg, M., & Larsson, N. (2016) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060815-014402 · Cited by 688
Self-citationOvarian ageing: the role of mitochondria in oocytes and follicles
May‐Panloup, P., Boucret, L., de la Barca, J.-M. C., Desquiret‐Dumas, V., Ferré-L’Hôtellier, V., Morinière, C., Descamps, P., Procaccio, V., & Reynier, P. (2016) · Human Reproduction Update · doi:10.1093/humupd/dmw028 · Cited by 585
Mammalian Mitochondria and Aging: An Update
Kauppila, T. E. S., Kauppila, J. H. K., & Larsson, N.-G. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2016.09.017 · Cited by 578
Self-citationMitochondrial allostatic load puts the 'gluc' back in glucocorticoids
Picard, M., Juster, R.-P., & McEwen, B. S. (2014) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2014.22 · Cited by 405
Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing
Latorre-Pellicer, A., Moreno-Loshuertos, R., Lechuga-Vieco, A. V., Sánchez-Cabo, F., Torroja, C., Acín-Pérez, R., Calvo, E., Aix, E., González-Guerra, A., Logan, A., et al. (2016) · Nature · doi:10.1038/nature18618 · Cited by 377
Bao, H., Cao, J., Chen, M., Min, C., Chen, W., Chen, X., Chen, Y., Chen, Y., Chen, Y., Chen, Z., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2305-0 · Cited by 402
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Jang, J. Y., Blum, A., Liu, J., & Finkel, T. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120842 · Cited by 358
Mitochondrial dysfunction in aging: Much progress but many unresolved questions
Payne, B. A. I., & Chinnery, P. F. (2015) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2015.05.022 · Cited by 335
Psychological Stress and Mitochondria: A Conceptual Framework
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Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals
Ye, K., Lü, J., Ma, F., Keinan, A., & Gu, Z. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1403521111 · Cited by 303
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Reddy, P., Ocampo, A., Suzuki, K., Luo, J., Bacman, S. R., Williams, S. L., Sugawara, A., Okamura, D., Tsunekawa, Y., Wu, J., et al. (2015) · Cell · doi:10.1016/j.cell.2015.03.051 · Cited by 302
Extreme heterogeneity of human mitochondrial DNA from organelles to populations
Stewart, J. B., & Chinnery, P. F. (2020) · Nature Reviews Genetics · doi:10.1038/s41576-020-00284-x · Cited by 260
Self-citationMitochondria in Ovarian Aging and Reproductive Longevity
Chiang, J. L., Shukla, P., Pagidas, K., Ahmed, N. S., Karri, S., Gunn, D. D., Hurd, W. W., & Singh, K. K. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101168 · Cited by 242
The genomic landscape of polymorphic human nuclear mitochondrial insertions
Dayama, G., Emery, S. B., Kidd, J. M., & Mills, R. E. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1038 · Cited by 245
Pleiotropic effects of mitochondria in aging
de Lima, T. I., Li, T. Y., Mottis, A., & Auwerx, J. H. (2022) · Nature Aging · doi:10.1038/s43587-022-00191-2 · Cited by 254
Lavrov, D. V., & Pett, W. (2016) · Genome Biology and Evolution · doi:10.1093/gbe/evw195 · Cited by 234
Genomic and epigenomic mechanisms of glucocorticoids in the brain
Gray, J. D., Kogan, J. F., Marrocco, J., & McEwen, B. S. (2017) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2017.97 · Cited by 242
Making Proteins in the Powerhouse
Hällberg, B. M., & Larsson, N. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.07.001 · Cited by 212
Self-citationKotiadis, V. N., Duchen, M. R., & Osellame, L. D. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.10.041 · Cited by 216
Mitochondrial proteostasis in the context of cellular and organismal health and aging
Moehle, E. A., Shen, K., & Dillin, A. G. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.tm117.000893 · Cited by 200
Mechanisms linking mtDNA damage and aging
Pinto, M., & Moraes, C. T. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.05.005 · Cited by 179
Changes of mitochondrial ultrastructure and function during ageing in mice and Drosophila
Brandt, T., Mourier, A., Tain, L. S., Partridge, L., Larsson, N., & Kühlbrandt, W. (2017) · eLife · doi:10.7554/elife.24662 · Cited by 186
Self-citationIndependent impacts of aging on mitochondrial DNA quantity and quality in humans
Zhang, R., Wang, Y., Ye, K., Picard, M. A., & Gu, Z. (2017) · BMC Genomics · doi:10.1186/s12864-017-4287-0 · Cited by 178
Greaves, L. C., Nooteboom, M., Elson, J. L., Tuppen, H. A. L., Taylor, G. A., Commane, D. M., Arasaradnam, R. P., Khrapko, K., Taylor, R. W., Kirkwood, T. B. L., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004620 · Cited by 172
Dobson, P. F., Dennis, E. P., Hipps, D., Reeve, A. K., Laude, A., Bradshaw, C., Stamp, C., Smith, A., Deehan, D. J., Turnbull, D. M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-68566-2 · Cited by 173
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Lazo, S., Hooten, N. N., Green, J., Eitan, E., Mode, N. A., Liu, Q., Zonderman, A. B., Ezike, N., Mattson, M. P., Ghosh, P., et al. (2020) · Aging Cell · doi:10.1111/acel.13283 · Cited by 163
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Samanta, S., He, Y., Sharma, A. K., Kim, J., Pan, W., Yang, Z., Li, J. W., Yan, W., Liu, L., Qu, J., et al. (2019) · Chem · doi:10.1016/j.chempr.2019.03.011 · Cited by 157
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Daniels, T. E., Olsen, E. M., & Tyrka, A. R. (2020) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-082719-104030 · Cited by 157
Zhang, K., Deng, R., Teng, X., Li, Y., Sun, Y., Ren, X., & Li, J. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b05309 · Cited by 144
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Jiang, M., Kauppila, T. E. S., Motori, E., Li, X., Atanassov, I., Folz‐Donahue, K., Bonekamp, N. A., Albarran-Gutierrez, S., Stewart, J. B., & Larsson, N. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.07.003 · Cited by 144
Self-citationKauppila, J. H. K., Baines, H. L., Bratić, A. M., Simard, M., Freyer, C., Mourier, A., Stamp, C., Filograna, R., Larsson, N., Greaves, L. C., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.037 · Cited by 143
Self-citationPhenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors
Pickett, S. J., Grady, J. P., Ng, Y. S., Gorman, G. S., Schaefer, A. M., Wilson, I., Cordell, H. J., Turnbull, D. M., Taylor, R. W., & McFarland, R. (2018) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.532 · Cited by 141
Smith, A. L. M., Whitehall, J. C., Bradshaw, C., Gay, D. M., Robertson, F. M., Blain, A. P., Hudson, G., Pyle, A., Houghton, D., Hunt, M., et al. (2020) · Nature Cancer · doi:10.1038/s43018-020-00112-5 · Cited by 140
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LaFountaine, J. S., Fathe, K., & Smyth, H. D. C. (2015) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2015.08.029 · Cited by 111
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains
Wei, W., Keogh, M. J., Wilson, I., Coxhead, J., Ryan, S., Rollinson, S. J., Griffin, H. R., Kurzawa‐Akanbi, M., Santibanez‐Koref, M., Talbot, K., et al. (2017) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0404-6 · Cited by 128
Potential factors result in diminished ovarian reserve: a comprehensive review
Zhu, Q., Li, Y., Ma, J., Ma, H., & Liang, X. (2023) · Journal of Ovarian Research · doi:10.1186/s13048-023-01296-x · Cited by 141
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Folgueras, A. R., Freitas-Rodríguez, S., Velasco, G., & López-Otín, C. (2018) · Circulation Research · doi:10.1161/circresaha.118.312204 · Cited by 113
Aryaman, J., Johnston, I. G., & Jones, N. S. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2018.00718 · Cited by 123
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Stewart, J. B., & Larsson, N. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004670 · Cited by 113
Self-citationAge-related accumulation of de novo mitochondrial mutations in mammalian oocytes and somatic tissues
Arbeithuber, B., Hester, J., Cremona, M. A., Stoler, N., Zaidi, A. A., Higgins, B., Anthony, K., Chiaromonte, F., Díaz, F. J., & Makova, K. D. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000745 · Cited by 115
The control of mtDNA replication during differentiation and development
John, J. C. S. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.10.036 · Cited by 113
Ross, J. M., Olson, L., & Coppotelli, G. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160819458 · Cited by 113
Self-citationUPRmt-mediated cytoprotection and organismal aging
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Mitofusin 1 is required for female fertility and to maintain ovarian follicular reserve
Zhang, M., Bener, M. B., Jiang, Z., Wang, T., Esencan, E., Scott, R., Horváth, T. L., & Seli, E. U. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1799-3 · Cited by 110
Mitophagy plays a central role in mitochondrial ageing
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Mitochondrial dysfunction and ovarian aging
Wang, T., Zhang, M., Jiang, Z., & Seli, E. U. (2017) · American Journal of Reproductive Immunology · doi:10.1111/aji.12651 · Cited by 109
No recombination of mtDNA after heteroplasmy for 50 generations in the mouse maternal germline
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Self-citationCause or casualty: The role of mitochondrial DNA in aging and age-associated disease
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Yang, L., Lin, X., Tang, H., Fan, Y., Zeng, S., Jia, L., Li, Y., Shi, Y., He, S., Wang, H., et al. (2020) · Aging Cell · doi:10.1111/acel.13206 · Cited by 108
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Hodgkinson, A., Idaghdour, Y., Gbeha, E., Grenier, J., Hip-Ki, E., Bruat, V., Goulet, J.-P., de Malliard, T., & Awadalla, P. (2014) · Science · doi:10.1126/science.1251110 · Cited by 101
Theurey, P., & Pizzo, P. (2018) · Genes · doi:10.3390/genes9010022 · Cited by 108
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Self-citationFocusing on mitochondria in the brain: from biology to therapeutics
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Li, M., Rothwell, R., Vermaat, M., Wachsmuth, M., Schröder, R., Laros, J. F. J., van Oven, M., Bakker, P. I. W. D., Bovenberg, J. A., van Duijn, C. M., et al. (2016) · Genome Research · doi:10.1101/gr.203216.115 · Cited by 101
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Aging: A mitochondrial DNA perspective, critical analysis and an update
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Beekman, M., Dowling, D. K., & Aanen, D. K. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0440 · Cited by 91
Kukreja, L., Kujoth, G. C., Prolla, T. A., LEUVEN, F. V., & Vassar, R. J. (2014) · Molecular Neurodegeneration · doi:10.1186/1750-1326-9-16 · Cited by 85
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Hurd, T. R., Herrmann, B., Sauerwald, J., Sanny, J., Grosch, M., & Lehmann, R. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.11.004 · Cited by 78
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Gaziev, A. I., Abdullaev, S., & Podlutsky, A. (2014) · Biogerontology · doi:10.1007/s10522-014-9515-2 · Cited by 77
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Kauppila, J. H. K., Bonekamp, N. A., Mourier, A., Isokallio, M. A., Just, A., Kauppila, T. E. S., Stewart, J. B., & Larsson, N. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky456 · Cited by 81
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Moro, L. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8111983 · Cited by 73
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Tower, J. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.10.008 · Cited by 68
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Li, Y., Wu, Y., Xu, R., Guo, J., Quan, F., Zhang, Y., Huang, D., Pei, Y., Gao, H., Liu, W., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43552-0 · Cited by 69
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Mitochondrial DNA Repair in Neurodegenerative Diseases and Ageing
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Metadata
- Authors
- Ross, J. M., Stewart, J. B., Hagström, E., Brené, S., Mourier, A., Coppotelli, G., Freyer, C., Lagouge, M., Hoffer, B. J., Olson, L., & Larsson, N.-G.
- Affiliations
- Karolinska Institutet (SE)
- Max Planck Institute for Biology of Ageing (DE)
- University Hospitals of Cleveland (US)
- Corresponding author
- Olson, Lars
- Larsson, Nils-Göran
- ORCID
- Venue
- Nature
- Published
- 2013-08-21
- Volume
- 501
- Issue
- 7467
- Pages
- 412-415
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3820420
- OpenAlex
- W2088995367
- Cited by
- 273
- References
- 33
- Citations by year
- 2026: 11 · 2025: 18 · 2024: 19 · 2023: 12 · 2022: 17 · 2021: 12 · 2020: 27 · 2019: 22 · 2018: 27 · 2017: 18 · 2016: 23 · 2015: 21 · 2014: 32 · 2013: 13
- FWCI
- 13.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- National Institute on Aging (AG04418, P01AG004418)
- National Institute of Neurological Disorders and Stroke (R01NS070825, NS 070825)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- aging, brain malformations, somatic mtDNA mutations, mitochondrial heteroplasmy, clonal expansion, respiratory chain deficiency, fertility, mouse mutants, mitochondrial dysfunction, brain development, somatic mosaicism
- MeSH terms
- Aging, Alleles, Animals, Brain, Cell Nucleus, DNA, Mitochondrial, Extrachromosomal Inheritance, Female, Heterozygote, Litter Size, Male, Mice, Inbred C57BL, Mitochondria, Mutation, Phenotype, Reproduction, Stochastic Processes, Mutagenesis, Genome, Mice
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