Detection and Analysis of DNA Methylation by Pyrosequencing
Hilary A. A. Colyer, Richard Neil Armstrong, Daniel Sharpe, Ken Mills
Abstract
Hilary A. A. Colyer, Richard Neil Armstrong, Daniel Sharpe, Ken Mills
Abstract
Pyrosequencing is a "sequencing by synthesis" technique which can be used to quantify DNA methylation at specific CpG sites within the target region of interest. Biotin labelled polymerase chain reaction (PCR) products form the template for base-pair nucleotide incorporation causing a light emitting cascade reaction resulting in the formation of a pyrogram and the calculation of the percentage methylation for each site. Prior to pyrosequencing, it is essential to bisulphite-convert the DNA sample and then perform locus-specific PCR for the region of interest. One of the PCR primers needs to be biotinylated and a separate sequencing primer is required for the pyrosequencing itself.
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Pyrosequencing is a "sequencing by synthesis" technique which can be used to quantify DNA methylation at specific CpG sites within the target region of interest. Biotin labelled polymerase chain reaction (PCR) products form the template for base-pair nucleotide incorporation causing a light emitting cascade reaction resulting in the formation of a pyrogram and the calculation of the percentage methylation for each site. Prior to pyrosequencing, it is essential to bisulphite-convert the DNA sample and then perform locus-specific PCR for the region of interest. One of the PCR primers needs to be biotinylated and a separate sequencing primer is required for the pyrosequencing itself.
Key concepts: Pyrosequencing, Bisulfite sequencing, Primer (cosmetics), Biology, Illumina Methylation Assay, CpG site, Polymerase chain reaction, Sequencing by ligation