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Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution
Mitochondria are involved in a number of diverse cellular functions, including energy production, metabolic regulation, apoptosis, calcium homeostasis, cell proliferation, and motility, as well as free radical generation. Mitochondrial DNA (mtDNA) is present at hundreds to thousands of copies per ce...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836731/ https://www.ncbi.nlm.nih.gov/pubmed/31548359 http://dx.doi.org/10.1101/gr.250480.119 |
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author | O'Hara, Ryan Tedone, Enzo Ludlow, Andrew Huang, Ejun Arosio, Beatrice Mari, Daniela Shay, Jerry W. |
author_facet | O'Hara, Ryan Tedone, Enzo Ludlow, Andrew Huang, Ejun Arosio, Beatrice Mari, Daniela Shay, Jerry W. |
author_sort | O'Hara, Ryan |
collection | PubMed |
description | Mitochondria are involved in a number of diverse cellular functions, including energy production, metabolic regulation, apoptosis, calcium homeostasis, cell proliferation, and motility, as well as free radical generation. Mitochondrial DNA (mtDNA) is present at hundreds to thousands of copies per cell in a tissue-specific manner. mtDNA copy number also varies during aging and disease progression and therefore might be considered as a biomarker that mirrors alterations within the human body. Here, we present a new quantitative, highly sensitive droplet digital PCR (ddPCR) method, droplet digital mitochondrial DNA measurement (ddMDM), to measure mtDNA copy number not only from cell populations but also from single cells. Our developed assay can generate data in as little as 3 h, is optimized for 96-well plates, and also allows the direct use of cell lysates without the need for DNA purification or nuclear reference genes. We show that ddMDM is able to detect differences between samples whose mtDNA copy number was close enough as to be indistinguishable by other commonly used mtDNA quantitation methods. By utilizing ddMDM, we show quantitative changes in mtDNA content per cell across a wide variety of physiological contexts including cancer progression, cell cycle progression, human T cell activation, and human aging. |
format | Online Article Text |
id | pubmed-6836731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68367312019-11-20 Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution O'Hara, Ryan Tedone, Enzo Ludlow, Andrew Huang, Ejun Arosio, Beatrice Mari, Daniela Shay, Jerry W. Genome Res Method Mitochondria are involved in a number of diverse cellular functions, including energy production, metabolic regulation, apoptosis, calcium homeostasis, cell proliferation, and motility, as well as free radical generation. Mitochondrial DNA (mtDNA) is present at hundreds to thousands of copies per cell in a tissue-specific manner. mtDNA copy number also varies during aging and disease progression and therefore might be considered as a biomarker that mirrors alterations within the human body. Here, we present a new quantitative, highly sensitive droplet digital PCR (ddPCR) method, droplet digital mitochondrial DNA measurement (ddMDM), to measure mtDNA copy number not only from cell populations but also from single cells. Our developed assay can generate data in as little as 3 h, is optimized for 96-well plates, and also allows the direct use of cell lysates without the need for DNA purification or nuclear reference genes. We show that ddMDM is able to detect differences between samples whose mtDNA copy number was close enough as to be indistinguishable by other commonly used mtDNA quantitation methods. By utilizing ddMDM, we show quantitative changes in mtDNA content per cell across a wide variety of physiological contexts including cancer progression, cell cycle progression, human T cell activation, and human aging. Cold Spring Harbor Laboratory Press 2019-11 /pmc/articles/PMC6836731/ /pubmed/31548359 http://dx.doi.org/10.1101/gr.250480.119 Text en © 2019 O'Hara et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Method O'Hara, Ryan Tedone, Enzo Ludlow, Andrew Huang, Ejun Arosio, Beatrice Mari, Daniela Shay, Jerry W. Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution |
title | Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution |
title_full | Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution |
title_fullStr | Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution |
title_full_unstemmed | Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution |
title_short | Quantitative mitochondrial DNA copy number determination using droplet digital PCR with single-cell resolution |
title_sort | quantitative mitochondrial dna copy number determination using droplet digital pcr with single-cell resolution |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836731/ https://www.ncbi.nlm.nih.gov/pubmed/31548359 http://dx.doi.org/10.1101/gr.250480.119 |
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