Allele-specific methylation analysis on upstream promoter region of H19 by methylation-specific PCR with confronting two-pair primers

生物 DNA甲基化 甲基化 分子生物学 发起人 亚硫酸氢盐测序 CpG站点 遗传学 表观遗传学 基因 差异甲基化区 照明菌甲基化试验
作者
Hiromi Sasamoto,Takeshi Nagasaka,Kenji Notohara,Kazuhide Ozaki,Hiroshi Isozaki,Noriaki Tanaka,Nagahide Matsubara
出处
期刊:International Journal of Oncology [Spandidos Publishing]
卷期号:25 (5): 1273-1278 被引量:13
标识
DOI:10.3892/ijo.25.5.1273
摘要

H19 and IGF2 genes are imprinted genes and expressed differently depending on whether they are carried by a chromosome of maternal or paternal origin; H19 is expressed only from the maternal allele and IGF2 only from the paternally inherited allele. The upstream promoter region of H19 has the imprinting-control region (ICR) or CTCF binding sites, where the methylation status of this region is critical to the regulation of imprinting of the H19/IGF2 locus located in chromosome 11p15. There are various reports on imprinting disorders in this region. In colorectal cancer aberrant biallelic methylation of CTCF binding site has been reported, and aberrant hypomethylation of this region in bladder cancer. Thus, certain human neoplasms have either hyper- or hypo-methylation in the ICR. Hence it is still difficult to analyze allele-specific methylation disorder of the region, or differentially methylated regions (DMR), locate upstream of H19. Here we report a new method, which could distinguish paternal epigenetic or maternal epigenetic pattern by a single PCR assay, to combine methylation-specific PCR and PCR with confronting two-pair primers (MSP-CTPP). Using this method, we investigated the region close to H19 ICR in 161 colorectal cancer and 65 gastric cancer cases.

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