Boyko Alex, Kovalchuk Igor
Department of Biological Sciences, University of Lethbridge, Lethbridge, AB, Canada.
Methods Mol Biol. 2010;631:23-31. doi: 10.1007/978-1-60761-646-7_3.
DNA methylation is a major mechanism for the reversible control of gene expression, chromatin structure, and genome stability. Methylation analysis at a given locus allows one to evaluate levels of chromatin packaging, gene expression, and even homologous recombination. We have shown that the combined bisulfite restriction analysis (COBRA) assay makes it possible to analyze methylation levels at a defined locus. The major steps are: bisulfite conversion of nonmethylate cytosines to uracils, locus-specific PCR amplification of converted DNA, restriction digestion, and analysis of restriction patterns on the gel. Due to the availability of various restriction enzymes that have cytosines in the restriction recognition sequence, the assay allows analysis of various cytosines, including those potentially targeted for symmetrical and nonsymmetrical methylation.
DNA甲基化是基因表达、染色质结构和基因组稳定性可逆调控的主要机制。对给定基因座进行甲基化分析可使人们评估染色质包装水平、基因表达甚至同源重组情况。我们已经表明,联合亚硫酸氢盐限制分析(COBRA)检测法能够分析特定基因座的甲基化水平。主要步骤如下:将未甲基化的胞嘧啶亚硫酸氢盐转化为尿嘧啶,对转化后的DNA进行基因座特异性PCR扩增,进行限制性酶切消化,以及分析凝胶上的限制性酶切图谱。由于在限制性识别序列中存在胞嘧啶的各种限制性内切酶可供使用,该检测法能够分析各种胞嘧啶,包括那些可能成为对称和非对称甲基化靶点的胞嘧啶。