Sequence-selective 5-methylcytosine oxidation for epigenotyping.

Akimitsu Okamoto, Kazuki Tainaka
Author Information
  1. Akimitsu Okamoto: Department of Synthetic Chemistry and Biological Chemistry, Faculty of Engineering, Kyoto University, Kyoto 615-8510, Japan.

Abstract

Methylation of DNA is an epigenetic modification that can play an important role in the control of gene expression in mammalian cells. The development of a simple and convenient method for site-specific discrimination of cytosine methylation is imperative for genomic studies. Here we report a facile method for distinguishing between cytosine and 5-methylcytosine. Osmium tetroxide caused the dihydroxylation of the C5-C6 double bond of 5-methylcytosine under an appropriate reaction conditions. The oxidation of 5-methylcytosine-containing target DNA was controlled by hybridization with a guide DNA. This technique facilitates the typing of cytosine methylation at a specific site of the target DNA.

MeSH Term

5-Methylcytosine
Base Sequence
Cytosine
DNA
DNA Methylation
Genotype
Hydroxylation
Nucleic Acid Hybridization
Osmium Tetroxide
Oxidation-Reduction

Chemicals

5-Methylcytosine
Cytosine
DNA
Osmium Tetroxide

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