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oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips

DNA methylation analysis has become an integral part of biomedical research. For high-throughput applications such as epigenome-wide association studies, the Infinium HumanMethylation450 (450K) BeadChip is currently the platform of choice. However, BeadChip processing relies on traditional bisulfite...

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Detalles Bibliográficos
Autores principales: Stewart, Sabrina K., Morris, Tiffany J., Guilhamon, Paul, Bulstrode, Harry, Bachman, Martin, Balasubramanian, Shankar, Beck, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304834/
https://www.ncbi.nlm.nih.gov/pubmed/25175075
http://dx.doi.org/10.1016/j.ymeth.2014.08.009
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author Stewart, Sabrina K.
Morris, Tiffany J.
Guilhamon, Paul
Bulstrode, Harry
Bachman, Martin
Balasubramanian, Shankar
Beck, Stephan
author_facet Stewart, Sabrina K.
Morris, Tiffany J.
Guilhamon, Paul
Bulstrode, Harry
Bachman, Martin
Balasubramanian, Shankar
Beck, Stephan
author_sort Stewart, Sabrina K.
collection PubMed
description DNA methylation analysis has become an integral part of biomedical research. For high-throughput applications such as epigenome-wide association studies, the Infinium HumanMethylation450 (450K) BeadChip is currently the platform of choice. However, BeadChip processing relies on traditional bisulfite (BS) based protocols which cannot discriminate between 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC). Here, we report the adaptation of the recently developed oxidative bisulfite (oxBS) chemistry to specifically detect both 5mC and 5hmC in a single workflow using 450K BeadChips, termed oxBS-450K. Supported by validation using mass spectrometry and pyrosequencing, we demonstrate reproducible (R(2) > 0.99) detection of 5hmC in human brain tissue using the optimised oxBS-450K protocol described here.
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spelling pubmed-43048342015-01-27 oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips Stewart, Sabrina K. Morris, Tiffany J. Guilhamon, Paul Bulstrode, Harry Bachman, Martin Balasubramanian, Shankar Beck, Stephan Methods Article DNA methylation analysis has become an integral part of biomedical research. For high-throughput applications such as epigenome-wide association studies, the Infinium HumanMethylation450 (450K) BeadChip is currently the platform of choice. However, BeadChip processing relies on traditional bisulfite (BS) based protocols which cannot discriminate between 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC). Here, we report the adaptation of the recently developed oxidative bisulfite (oxBS) chemistry to specifically detect both 5mC and 5hmC in a single workflow using 450K BeadChips, termed oxBS-450K. Supported by validation using mass spectrometry and pyrosequencing, we demonstrate reproducible (R(2) > 0.99) detection of 5hmC in human brain tissue using the optimised oxBS-450K protocol described here. Academic Press 2015-01-15 /pmc/articles/PMC4304834/ /pubmed/25175075 http://dx.doi.org/10.1016/j.ymeth.2014.08.009 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Stewart, Sabrina K.
Morris, Tiffany J.
Guilhamon, Paul
Bulstrode, Harry
Bachman, Martin
Balasubramanian, Shankar
Beck, Stephan
oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips
title oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips
title_full oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips
title_fullStr oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips
title_full_unstemmed oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips
title_short oxBS-450K: A method for analysing hydroxymethylation using 450K BeadChips
title_sort oxbs-450k: a method for analysing hydroxymethylation using 450k beadchips
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304834/
https://www.ncbi.nlm.nih.gov/pubmed/25175075
http://dx.doi.org/10.1016/j.ymeth.2014.08.009
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