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Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products

BACKGROUND: To utilize the power of high-throughput sequencers, target enrichment methods have been developed. The majority of these require reagents and equipment that are only available from commercial vendors and are not suitable for the targets that are a few kilobases in length. METHODOLOGY/PRI...

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Detalles Bibliográficos
Autores principales: Maricic, Tomislav, Whitten, Mark, Pääbo, Svante
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2982832/
https://www.ncbi.nlm.nih.gov/pubmed/21103372
http://dx.doi.org/10.1371/journal.pone.0014004
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author Maricic, Tomislav
Whitten, Mark
Pääbo, Svante
author_facet Maricic, Tomislav
Whitten, Mark
Pääbo, Svante
author_sort Maricic, Tomislav
collection PubMed
description BACKGROUND: To utilize the power of high-throughput sequencers, target enrichment methods have been developed. The majority of these require reagents and equipment that are only available from commercial vendors and are not suitable for the targets that are a few kilobases in length. METHODOLOGY/PRINCIPAL FINDINGS: We describe a novel and economical method in which custom made long-range PCR products are used to capture complete human mitochondrial genomes from complex DNA mixtures. We use the method to capture 46 complete mitochondrial genomes in parallel and we sequence them on a single lane of an Illumina GA(II) instrument. CONCLUSIONS/SIGNIFICANCE: This method is economical and simple and particularly suitable for targets that can be amplified by PCR and do not contain highly repetitive sequences such as mtDNA. It has applications in population genetics and forensics, as well as studies of ancient DNA.
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spelling pubmed-29828322010-11-22 Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products Maricic, Tomislav Whitten, Mark Pääbo, Svante PLoS One Research Article BACKGROUND: To utilize the power of high-throughput sequencers, target enrichment methods have been developed. The majority of these require reagents and equipment that are only available from commercial vendors and are not suitable for the targets that are a few kilobases in length. METHODOLOGY/PRINCIPAL FINDINGS: We describe a novel and economical method in which custom made long-range PCR products are used to capture complete human mitochondrial genomes from complex DNA mixtures. We use the method to capture 46 complete mitochondrial genomes in parallel and we sequence them on a single lane of an Illumina GA(II) instrument. CONCLUSIONS/SIGNIFICANCE: This method is economical and simple and particularly suitable for targets that can be amplified by PCR and do not contain highly repetitive sequences such as mtDNA. It has applications in population genetics and forensics, as well as studies of ancient DNA. Public Library of Science 2010-11-16 /pmc/articles/PMC2982832/ /pubmed/21103372 http://dx.doi.org/10.1371/journal.pone.0014004 Text en Maricic et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Maricic, Tomislav
Whitten, Mark
Pääbo, Svante
Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
title Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
title_full Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
title_fullStr Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
title_full_unstemmed Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
title_short Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
title_sort multiplexed dna sequence capture of mitochondrial genomes using pcr products
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2982832/
https://www.ncbi.nlm.nih.gov/pubmed/21103372
http://dx.doi.org/10.1371/journal.pone.0014004
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