Pogribny I P, Poirier L A, James S J
Division of Nutritional Toxicology, National Center for Toxicological Research, Food and Drug Administration, Jefferson, AR 72079, USA.
Carcinogenesis. 1995 Nov;16(11):2863-7. doi: 10.1093/carcin/16.11.2863.
Dietary folate/methyl deficiency provides a unique model of endogenous hepatocarcinogenesis in which to study progressive alterations in DNA methylation patterns during tumor progression in vivo. Weanling male F344 rats were given a semi-purified diet deficient in the methyl donors choline, methionine and folic acid for a period of 9 weeks. Using a genomic sequencing procedure based on the PCR amplification of bisulfite-modified DNA, the methylation status of individual CpG sites within exons 6 and 7 of the p53 gene in liver samples from control and deficient rats was determined. Treatment of denatured nuclear DNA with sodium bisulfite quantitatively converts all cytosine residues to uracil which are then amplified as thymine in the PCR reaction. In contrast, 5-methylcytosine is resistant to bisulfite deamination under the reaction conditions and is amplified as cytosine. Automated sequencing of bisulfite-modified DNA will then elucidate the methylation status of each cytosine residue within a defined gene sequence. In addition to evaluation of the methylation status of the p53 gene, the relative activity of the DNA methyltransferase was also quantified in nuclear extracts from control and folate/methyl deficient rats. The results indicate that specific 5-methyl cytosines within the hepatic p53 gene from methyl deficient rats are resistant to demethylation despite the diet-induced decrease in S-adenosylmethionine and the increase in cell proliferation associated with this dietary intervention. Progressive demethylation was observed at other methylated cytosine residues in folate/methyl deficient rats after 9 weeks despite a paradoxical increase in DNA methyltransferase activity. The application of this sequence-specific technology will allow the definition of the methylation status of every CpG site within a coding sequence or promoter region and should provide new insights into mechanisms and consequences of methylation dysregulation during progressive multistage carcinogenesis.
膳食叶酸/甲基缺乏提供了一种内源性肝癌发生的独特模型,可用于研究体内肿瘤进展过程中DNA甲基化模式的渐进性改变。将断奶雄性F344大鼠给予缺乏甲基供体胆碱、蛋氨酸和叶酸的半纯化饮食9周。使用基于亚硫酸氢盐修饰DNA的PCR扩增的基因组测序程序,确定来自对照和缺乏饮食大鼠肝脏样本中p53基因外显子6和7内单个CpG位点的甲基化状态。用亚硫酸氢钠处理变性核DNA可将所有胞嘧啶残基定量转化为尿嘧啶,然后在PCR反应中作为胸腺嘧啶进行扩增。相反,5-甲基胞嘧啶在反应条件下对亚硫酸氢盐脱氨具有抗性,并作为胞嘧啶进行扩增。亚硫酸氢盐修饰DNA的自动测序将阐明定义基因序列内每个胞嘧啶残基的甲基化状态。除了评估p53基因的甲基化状态外,还对来自对照和叶酸/甲基缺乏大鼠的核提取物中DNA甲基转移酶的相对活性进行了定量。结果表明,尽管饮食诱导S-腺苷甲硫氨酸减少以及与这种饮食干预相关的细胞增殖增加,但来自甲基缺乏大鼠肝脏p53基因内的特定5-甲基胞嘧啶对去甲基化具有抗性。尽管DNA甲基转移酶活性出现反常增加,但在9周后,叶酸/甲基缺乏大鼠的其他甲基化胞嘧啶残基处观察到渐进性去甲基化。这种序列特异性技术的应用将允许定义编码序列或启动子区域内每个CpG位点的甲基化状态,并应为多阶段渐进性癌变过程中甲基化失调机制及后果提供新见解。