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DNA methylation analysis using metal complex formation
Author(s) -
Akimitsu Okamoto,
Kazuo Tanaka,
Keiichi Tainaka,
T. Umemoto,
Akiko Nomura
Publication year - 2007
Publication title -
nucleic acids symposium series
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/nrm014
Subject(s) - dna methylation , cytosine , methylation , osmium , dna , chemistry , gene , biochemistry , gene expression , biology , microbiology and biotechnology , ruthenium , catalysis
Analysis of the cytosine methylation status of a gene is very important for understanding the expression mechanism of genetic information. However, to distinguish 5-methylcytosine (M) from C, i.e., to detect the existence of only one methyl group in a long DNA strand, is not easy. A rapid and selective chemical reaction capable of distinguishing between M and C would become a useful method for efficiently analyzing the status of cytosine methylation at a specific site in a gene. We herein report M-selective oxidation. M was oxidized efficiently by exposure to a reaction mixture containing an osmium complex, making possible a clear distinction from very weak oxidation of C. We readily obtained information on the methylation status at a specific site by means of M-selective oxidation using functional bipyridine ligands.

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