Okazaki Ryuji, Ootsuyama Akira, Yoshida Yasuhiro, Norimura Toshiyuki
Department of Radiation Biology and Health, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka Yahatanishi-ku, Kitakyushu 807-8555, Japan.
Mol Biol Int. 2011;2011:938435. doi: 10.4061/2011/938435. Epub 2011 Dec 12.
Methylation-specific PCR (MSP) of the mouse p53 gene has not yet been reported. We searched the CpG islands, sequenced the bisulfited DNA, and designed PCR primers for methylation and unmethylation sites. DNA from a young mouse produced a strong PCR product with the unmethylated primer and a weaker band with the methylated primer. DNA from an old mouse produced bands of similar intensities with both primers. In radiation-induced tumors, DNA from an old mouse yielded similar bands with both types of primers. We suggest that MSP is a valuable technique for the epigenetic study of the mouse p53 gene.
小鼠p53基因的甲基化特异性PCR(MSP)尚未见报道。我们搜索了CpG岛,对亚硫酸氢盐处理后的DNA进行测序,并针对甲基化和非甲基化位点设计了PCR引物。来自年轻小鼠的DNA与非甲基化引物产生了强PCR产物,与甲基化引物产生了较弱的条带。来自老年小鼠的DNA与两种引物产生的条带强度相似。在辐射诱导的肿瘤中,老年小鼠的DNA与两种类型的引物都产生了相似的条带。我们认为MSP是用于小鼠p53基因表观遗传学研究的一种有价值的技术。