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Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay

Mitochondrial dysfunction is implicated in a vast array of diseases and conditions, such as Alzheimer's disease, cancer, and aging. Alterations in mitochondrial DNA (mtDNA) may provide insight into the processes that either initiate or propagate this dysfunction. Here, we describe a unique mult...

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Detalles Bibliográficos
Autores principales: Phillips, Nicole R., Sprouse, Marc L., Roby, Rhonda K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894387/
https://www.ncbi.nlm.nih.gov/pubmed/24463429
http://dx.doi.org/10.1038/srep03887
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author Phillips, Nicole R.
Sprouse, Marc L.
Roby, Rhonda K.
author_facet Phillips, Nicole R.
Sprouse, Marc L.
Roby, Rhonda K.
author_sort Phillips, Nicole R.
collection PubMed
description Mitochondrial dysfunction is implicated in a vast array of diseases and conditions, such as Alzheimer's disease, cancer, and aging. Alterations in mitochondrial DNA (mtDNA) may provide insight into the processes that either initiate or propagate this dysfunction. Here, we describe a unique multiplex assay which simultaneously provides assessments of mtDNA copy number and the proportion of genomes with common large deletions by targeting two mitochondrial sites and one nuclear locus. This probe-based, single-tube multiplex provides high specificity while eliminating well-to-well variability that results from assaying nuclear and mitochondrial targets individually.
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spelling pubmed-48943872016-06-10 Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay Phillips, Nicole R. Sprouse, Marc L. Roby, Rhonda K. Sci Rep Article Mitochondrial dysfunction is implicated in a vast array of diseases and conditions, such as Alzheimer's disease, cancer, and aging. Alterations in mitochondrial DNA (mtDNA) may provide insight into the processes that either initiate or propagate this dysfunction. Here, we describe a unique multiplex assay which simultaneously provides assessments of mtDNA copy number and the proportion of genomes with common large deletions by targeting two mitochondrial sites and one nuclear locus. This probe-based, single-tube multiplex provides high specificity while eliminating well-to-well variability that results from assaying nuclear and mitochondrial targets individually. Nature Publishing Group 2014-01-27 /pmc/articles/PMC4894387/ /pubmed/24463429 http://dx.doi.org/10.1038/srep03887 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Phillips, Nicole R.
Sprouse, Marc L.
Roby, Rhonda K.
Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay
title Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay
title_full Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay
title_fullStr Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay
title_full_unstemmed Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay
title_short Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: A multiplex real-time PCR assay
title_sort simultaneous quantification of mitochondrial dna copy number and deletion ratio: a multiplex real-time pcr assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894387/
https://www.ncbi.nlm.nih.gov/pubmed/24463429
http://dx.doi.org/10.1038/srep03887
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