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Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform
DNA methylation is the best-studied epigenetic modification and describes the conversion of cytosine to 5-methylcytosine. The importance of this phenomenon is that aberrant promoter hypermethylation is a common occurrence in cancer and is frequently associated with gene silencing. Various techniques...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1361623/ https://www.ncbi.nlm.nih.gov/pubmed/16464820 http://dx.doi.org/10.1093/nar/gnj017 |
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author | Brena, Romulo Martin Auer, Herbert Kornacker, Karl Hackanson, Björn Raval, Aparna Byrd, John C. Plass, Christoph |
author_facet | Brena, Romulo Martin Auer, Herbert Kornacker, Karl Hackanson, Björn Raval, Aparna Byrd, John C. Plass, Christoph |
author_sort | Brena, Romulo Martin |
collection | PubMed |
description | DNA methylation is the best-studied epigenetic modification and describes the conversion of cytosine to 5-methylcytosine. The importance of this phenomenon is that aberrant promoter hypermethylation is a common occurrence in cancer and is frequently associated with gene silencing. Various techniques are currently available for the analysis of DNA methylation. However, accurate and reproducible quantification of DNA methylation remains challenging. In this report, we describe Bio-COBRA (combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform), as a novel approach to quantitative DNA methylation analysis. The combination of a well-established method, COBRA, which interrogates DNA methylation via the restriction enzyme analysis of PCR-amplified bisulfite treated DNAs, with the Bioanalyzer platform allows for the rapid and quantitative assessment of DNA methylation patterns in large sample sets. The sensitivity and reproducibility of Bio-COBRA make it a valuable tool for the analysis of DNA methylation in clinical samples, which could aid in the development of diagnostic and prognostic parameters with respect to disease detection and management. |
format | Text |
id | pubmed-1361623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-13616232006-02-09 Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform Brena, Romulo Martin Auer, Herbert Kornacker, Karl Hackanson, Björn Raval, Aparna Byrd, John C. Plass, Christoph Nucleic Acids Res Methods Online DNA methylation is the best-studied epigenetic modification and describes the conversion of cytosine to 5-methylcytosine. The importance of this phenomenon is that aberrant promoter hypermethylation is a common occurrence in cancer and is frequently associated with gene silencing. Various techniques are currently available for the analysis of DNA methylation. However, accurate and reproducible quantification of DNA methylation remains challenging. In this report, we describe Bio-COBRA (combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform), as a novel approach to quantitative DNA methylation analysis. The combination of a well-established method, COBRA, which interrogates DNA methylation via the restriction enzyme analysis of PCR-amplified bisulfite treated DNAs, with the Bioanalyzer platform allows for the rapid and quantitative assessment of DNA methylation patterns in large sample sets. The sensitivity and reproducibility of Bio-COBRA make it a valuable tool for the analysis of DNA methylation in clinical samples, which could aid in the development of diagnostic and prognostic parameters with respect to disease detection and management. Oxford University Press 2006 2006-02-07 /pmc/articles/PMC1361623/ /pubmed/16464820 http://dx.doi.org/10.1093/nar/gnj017 Text en © The Author 2006. Published by Oxford University Press. All rights reserved |
spellingShingle | Methods Online Brena, Romulo Martin Auer, Herbert Kornacker, Karl Hackanson, Björn Raval, Aparna Byrd, John C. Plass, Christoph Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform |
title | Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform |
title_full | Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform |
title_fullStr | Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform |
title_full_unstemmed | Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform |
title_short | Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform |
title_sort | accurate quantification of dna methylation using combined bisulfite restriction analysis coupled with the agilent 2100 bioanalyzer platform |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1361623/ https://www.ncbi.nlm.nih.gov/pubmed/16464820 http://dx.doi.org/10.1093/nar/gnj017 |
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