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Lookup NU author(s): Dr Brendan PayneORCiD, Dr Lynsey Cree, Professor Patrick Chinnery
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© Springer Science+Business Media New York 2015. All right reserved. Understanding the biology of mitochondrial DNA (mtDNA) at the single-cell level has yielded important insights into inheritance, disease, and normal aging. In nuclear gene disorders of mtDNA maintenance, neurodegeneration, and aging, different somatic mtDNA mutations exist within individual cells and may be missed by techniques applied to whole tissue DNA extract. We therefore provide a method for characterizing mtDNA within single skeletal muscle fibers. During embryogenesis, mtDNA content is subject to a tight bottleneck and this may account for differential segregation of mutant mtDNA in offspring. We also present a method to study this phenomenon by single-cell analysis of embryonic PGCs (primordial germ cells).
Author(s): Payne BAI, Cree L, Chinnery PF
Editor(s): Weissig V; Edeas M
Publication type: Book Chapter
Publication status: Published
Book Title: Mitochondrial Medicine
Year: 2015
Volume: 1264
Pages: 67-76
Print publication date: 29/01/2015
Online publication date: 06/01/2015
Acceptance date: 01/01/1900
Series Title: Methods in Molecular Biology
Publisher: Springer New York
Place Published: New York, NY, USA
URL: https://doi.org/10.1007/978-1-4939-2257-4_7
DOI: 10.1007/978-1-4939-2257-4_7
Notes: 9781493922567 Hardback ISBN
Library holdings: Search Newcastle University Library for this item
ISBN: 9781493922574