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Nat Protoc. 2012 Mar 8;7(4):617-36. doi: 10.1038/nprot.2012.012.

Methylome analysis using MeDIP-seq with low DNA concentrations.

Author information

1
University College London (UCL) Cancer Institute, University College London, London, UK. t.taiwo@ucl.ac.uk

Abstract

DNA methylation is an epigenetic mark that has a crucial role in many biological processes. To understand the functional consequences of DNA methylation on phenotypic plasticity, a genome-wide analysis should be embraced. This in turn requires a technique that balances accuracy, genome coverage, resolution and cost, yet is low in DNA input in order to minimize the drain on precious samples. Methylated DNA immunoprecipitation-sequencing (MeDIP-seq) fulfils these criteria, combining MeDIP with massively parallel DNA sequencing. Here we report an improved protocol using 100-fold less genomic DNA than that commonly used. We show comparable results for specificity (>97%) and enrichment (>100-fold) over a wide range of DNA concentrations (5,000-50 ng) and demonstrate the utility of the protocol for the generation of methylomes from rare bone marrow cells using 160-300 ng of starting DNA. The protocol described here, i.e., DNA extraction to generation of MeDIP-seq library, can be completed within 3-5 d.

PMID:
22402632
DOI:
10.1038/nprot.2012.012
[Indexed for MEDLINE]

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