Wang Yan, Zheng Wenli, Luo Junfeng, Zhang Dingdong, Zuhong Lu
The State Key Laboratory of Bioelectronics, Department of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.
Anal Biochem. 2006 Dec 15;359(2):183-8. doi: 10.1016/j.ab.2006.09.001. Epub 2006 Sep 25.
Increasing interest in DNA methylation has resulted in the recent development of array-based methods. However, these method require complex sample treatment processes, such as bisulfite modification in the liquid state of every sample. Here, we describe a microarray-based technology for interrogating DNA methylation status of multiple DNA samples at the same time, in which the DNA samples are first dotted on membranes and then treated with bisulfite directly. In this assay, plasmid pUC19 DNA is immobilized on nylon membranes and soaked in bisulfite reaction mixtures for 16h to convert unmethylated Cs to Us, and methylated Cs remain unchanged. The probes for detecting the methylation patterns of CpG sites are hybridized with the converted DNA dotted on the membranes, and the signals are revealed by chemiluminescence of DIG-labeled probes. The experiments show that this method can simplify the experimental processes and increase the efficiency of the bisulfite treatment. This new method could be used as a convenient tool for detecting the methylation status of multiple genes for a large number of samples in the future.
对DNA甲基化的兴趣日益增加,导致了基于芯片方法的最新发展。然而,这些方法需要复杂的样品处理过程,例如对每个样品的液态进行亚硫酸氢盐修饰。在这里,我们描述了一种基于微阵列的技术,用于同时检测多个DNA样品的DNA甲基化状态,其中DNA样品首先点样在膜上,然后直接用亚硫酸氢盐处理。在该检测中,质粒pUC19 DNA固定在尼龙膜上,并在亚硫酸氢盐反应混合物中浸泡16小时,以将未甲基化的C转化为U,而甲基化的C保持不变。用于检测CpG位点甲基化模式的探针与点样在膜上的转化后的DNA杂交,信号通过DIG标记探针的化学发光显示。实验表明,该方法可以简化实验过程,提高亚硫酸氢盐处理的效率。这种新方法将来可作为一种方便的工具,用于检测大量样品中多个基因的甲基化状态。