The low abundance of clonally expanded mitochondrial DNA point mutations in aged substantia nigra neurons

  • Clonally expanded mitochondrial DNA (mtDNA) deletions accumulate with age in human substantia nigra (SN) and high levels cause respiratory chain deficiency. In other human tissues, mtDNA point mutations clonally expand with age. Here, the abundance of mtDNA point mutations within single SN neurons from aged controls was investigated. From 31 single cytochrome c oxidase normal SN neurons, only one clonally expanded mtDNA point mutation was identified, suggesting in these neurons mtDNA point mutations occur rarely, whereas mtDNA deletions are frequently observed. This contrasts observations in mitotic tissues and suggests that different forms of mtDNA maintenance may exist in these two cell types.

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Metadaten
Author:Amy K. Reeve, Kim J. Krishnan, Geoffrey Taylor, Joanna L. Elson, Andreas BenderGND, Robert W. Taylor, Christopher M. Morris, Doug M. Turnbull
URN:urn:nbn:de:bvb:384-opus4-1139738
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/113973
ISSN:1474-9718OPAC
ISSN:1474-9726OPAC
Parent Title (English):Aging Cell
Publisher:Wiley
Place of publication:Weinheim
Type:Article
Language:English
Year of first Publication:2009
Publishing Institution:Universität Augsburg
Release Date:2024/07/11
Volume:8
Issue:4
First Page:496
Last Page:498
DOI:https://doi.org/10.1111/j.1474-9726.2009.00492.x
Institutes:Medizinische Fakultät
Medizinische Fakultät / Lehrstuhl für Neurorehabilitation
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Licence (German):Sonstige Open-Access-Lizenz