4.8 Article

Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA

Journal

NUCLEIC ACIDS RESEARCH
Volume 40, Issue 4, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkr1207

Keywords

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Funding

  1. Wellcome Trust
  2. Medical Research Council
  3. Cancer Research UK
  4. European Molecular Biology Organization
  5. Lister Institute of Preventative Medicine
  6. Ludwig Institute for Cancer Research Ltd
  7. Nuffield Department of Clinical Medicine
  8. Medical Research Council [G1000801a, MC_UU_12009/8] Funding Source: researchfish
  9. MRC [MC_UU_12009/8] Funding Source: UKRI

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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.

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