Electrochemical detection of 5-methylcytosine in bisulfite-treated DNA

被引:21
作者
Bartosik, Martin [1 ,2 ]
Fojta, Miroslav [1 ,3 ]
Palecek, Emil [1 ]
机构
[1] Acad Sci Czech Republ, Inst Biophys, Vvi, CS-61265 Brno, Czech Republic
[2] Masaryk Mem Canc Inst, Brno 65653, Czech Republic
[3] Masaryk Univ, Cent European Inst Technol, CZ-62500 Brno, Czech Republic
关键词
DNA methylation; 5-Methylcytosine analysis; Sodium bisulfite; Mercury electrode; Solid amalgam electrode; NUCLEIC-ACID BASES; POLAROGRAPHIC-BEHAVIOR; STRIPPING VOLTAMMETRY; OSZILLOGRAPHISCHE POLAROGRAPHIE; SUBMICROMOLAR CONCENTRATIONS; CYTOSINE METHYLATION; AMALGAM ELECTRODES; MERCURY-ELECTRODE; CPG ISLAND; GENE;
D O I
10.1016/j.electacta.2012.05.115
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
DNA methylation is an important epigenetic event playing crucial roles in physiologic and pathologic processes. We show that methylation of cytosine (C) residues in DNA can be easily detected electrochemically using mercury or solid amalgam electrodes. Reduction peaks of untreated single-stranded methylated and non-methylated oligodeoxynucleotides (ODN) do not significantly differ. Using DNA bisulfite treatment, reducible Cs are transformed into nonreducible uracil residues, strongly decreasing square wave voltammetric C reduction peaks. On the other hand. 5-methylcytosine (mC) residues resist the bisulfite treatment and display almost unchanged reduction peak. Desulfonation step should be omitted because uracil sulfonation improves the resolution of C from mC. By combining DNA bisulfite treatment with square wave voltammetry. DNA methylation can be determined quantitatively at nanomolar and subnamolar ODN concentrations. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
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