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Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA
Across vertebrate genomes methylation of cytosine residues within the context of CpG dinucleotides is a pervasive epigenetic mark that can impact gene expression and has been implicated in various developmental and disease-associated processes. Several biochemical approaches exist to profile DNA met...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287171/ https://www.ncbi.nlm.nih.gov/pubmed/22156374 http://dx.doi.org/10.1093/nar/gkr1207 |
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author | Blackledge, Neil P. Long, Hannah K. Zhou, Jin C. Kriaucionis, Skirmantas Patient, Roger Klose, Robert J. |
author_facet | Blackledge, Neil P. Long, Hannah K. Zhou, Jin C. Kriaucionis, Skirmantas Patient, Roger Klose, Robert J. |
author_sort | Blackledge, Neil P. |
collection | PubMed |
description | Across vertebrate genomes methylation of cytosine residues within the context of CpG dinucleotides is a pervasive epigenetic mark that can impact gene expression and has been implicated in various developmental and disease-associated processes. Several biochemical approaches exist to profile DNA methylation, but recently an alternative approach based on profiling non-methylated CpGs was developed. This technique, called CxxC affinity purification (CAP), uses a ZF-CxxC (CxxC) domain to specifically capture DNA containing clusters of non-methylated CpGs. Here we describe a new CAP approach, called biotinylated CAP (Bio-CAP), which eliminates the requirement for specialized equipment while dramatically improving and simplifying the CxxC-based DNA affinity purification. Importantly, this approach isolates non-methylated DNA in a manner that is directly proportional to the density of non-methylated CpGs, and discriminates non-methylated CpGs from both methylated and hydroxymethylated CpGs. Unlike conventional CAP, Bio-CAP can be applied to nanogram quantities of genomic DNA and in a magnetic format is amenable to efficient parallel processing of samples. Furthermore, Bio-CAP can be applied to genome-wide profiling of non-methylated DNA with relatively small amounts of input material. Therefore, Bio-CAP is a simple and streamlined approach for characterizing regions of the non-methylated DNA, whether at specific target regions or genome wide. |
format | Online Article Text |
id | pubmed-3287171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32871712012-02-27 Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA Blackledge, Neil P. Long, Hannah K. Zhou, Jin C. Kriaucionis, Skirmantas Patient, Roger Klose, Robert J. Nucleic Acids Res Methods Online Across vertebrate genomes methylation of cytosine residues within the context of CpG dinucleotides is a pervasive epigenetic mark that can impact gene expression and has been implicated in various developmental and disease-associated processes. Several biochemical approaches exist to profile DNA methylation, but recently an alternative approach based on profiling non-methylated CpGs was developed. This technique, called CxxC affinity purification (CAP), uses a ZF-CxxC (CxxC) domain to specifically capture DNA containing clusters of non-methylated CpGs. Here we describe a new CAP approach, called biotinylated CAP (Bio-CAP), which eliminates the requirement for specialized equipment while dramatically improving and simplifying the CxxC-based DNA affinity purification. Importantly, this approach isolates non-methylated DNA in a manner that is directly proportional to the density of non-methylated CpGs, and discriminates non-methylated CpGs from both methylated and hydroxymethylated CpGs. Unlike conventional CAP, Bio-CAP can be applied to nanogram quantities of genomic DNA and in a magnetic format is amenable to efficient parallel processing of samples. Furthermore, Bio-CAP can be applied to genome-wide profiling of non-methylated DNA with relatively small amounts of input material. Therefore, Bio-CAP is a simple and streamlined approach for characterizing regions of the non-methylated DNA, whether at specific target regions or genome wide. Oxford University Press 2012-02 2011-12-10 /pmc/articles/PMC3287171/ /pubmed/22156374 http://dx.doi.org/10.1093/nar/gkr1207 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Blackledge, Neil P. Long, Hannah K. Zhou, Jin C. Kriaucionis, Skirmantas Patient, Roger Klose, Robert J. Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA |
title | Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA |
title_full | Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA |
title_fullStr | Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA |
title_full_unstemmed | Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA |
title_short | Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA |
title_sort | bio-cap: a versatile and highly sensitive technique to purify and characterise regions of non-methylated dna |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287171/ https://www.ncbi.nlm.nih.gov/pubmed/22156374 http://dx.doi.org/10.1093/nar/gkr1207 |
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