J 2012

Electrochemical detection of 5-methylcytosine in bisulfite-treated DNA

BARTOSIK, Martin, Miroslav FOJTA and Emil PALECEK

Basic information

Original name

Electrochemical detection of 5-methylcytosine in bisulfite-treated DNA

Authors

BARTOSIK, Martin (203 Czech Republic), Miroslav FOJTA (203 Czech Republic, guarantor, belonging to the institution) and Emil PALECEK (203 Czech Republic)

Edition

Electrochimica Acta, Oxford, Pergamon-Elsevier Science, 2012, 0013-4686

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

10610 Biophysics

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

není předmětem státního či obchodního tajemství

Impact factor

Impact factor: 3.777

RIV identification code

RIV/00216224:14740/12:00073027

Organization unit

Central European Institute of Technology

UT WoS

000308259500010

Keywords in English

DNA methylation; 5-Methylcytosine analysis; Sodium bisulfite; Mercury electrode; Solid amalgam electrode

Tags

Tags

International impact, Reviewed
Změněno: 13/4/2014 10:30, Olga Křížová

Abstract

V originále

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.