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大鼠胃蛋白酶原基因在胚胎、成年和肿瘤组织中的DNA甲基化与表达

DNA methylation and expression of the rat pepsinogen gene in embryonic, adult, and neoplastic tissues.

作者信息

Ichinose M, Miki K, Furihata C, Tatematsu M, Ichihara Y, Ishihara T, Katsura I, Sogawa K, Fujii-Kuriyama Y, Tanji M

机构信息

Department of Biophysics and Biochemistry, Faculty of Science, University of Tokyo, Japan.

出版信息

Cancer Res. 1988 Mar 15;48(6):1603-9.

PMID:3345531
Abstract

The relationship between methylation and expression of rat pepsinogen 1 (Pg1) genes was investigated in various tissues. On Northern blotting with a Pg1 complementary DNA probe, Pg1 mRNA was detected only in the glandular stomach of normal rats. Methylation analysis with Msp1/HpaII and Hha1 revealed tissue specific methylation patterns of Pg1 genes with less methylated in the stomach than in other normal tissues not expressing the genes. During stomach development, there was a progressive increase in the Pg1 mRNA level that almost coincided with change in the mucosal pepsinogen level and progressive demethylation after the onset of transcription. Thus, there was an inverse correlation between methylation and expression of Pg1 genes, suggesting a role of DNA methylation in Pg1 gene regulation during normal differentiation, although not its primary role in gene activation. There was no detectable Pg1 mRNA in either primary or transplanted stomach cancers induced by N-methyl-N'-nitro-N-nitrosoguanidine. The methylation patterns of Pg1 genes were different from those of normal tissues that expressed the gene and of those that did not and no simple correlation was observed between methylation and expression of Pg1 genes. This result is consistent with a previous finding that DNA methylation is deranged in tumor cells.

摘要

研究了大鼠胃蛋白酶原1(Pg1)基因甲基化与表达在各种组织中的关系。用Pg1互补DNA探针进行Northern印迹分析时,仅在正常大鼠的腺胃中检测到Pg1 mRNA。用Msp1/HpaII和Hha1进行甲基化分析显示,Pg1基因存在组织特异性甲基化模式,胃中的甲基化程度低于其他不表达该基因的正常组织。在胃发育过程中,Pg1 mRNA水平逐渐升高,这几乎与黏膜胃蛋白酶原水平的变化以及转录开始后的逐渐去甲基化同时发生。因此,Pg1基因的甲基化与表达呈负相关,这表明DNA甲基化在正常分化过程中对Pg1基因调控起作用,尽管它在基因激活中并非主要作用。在N-甲基-N'-硝基-N-亚硝基胍诱导的原发性或移植性胃癌中均未检测到Pg1 mRNA。Pg1基因的甲基化模式与表达该基因的正常组织以及不表达该基因的正常组织不同,且未观察到Pg1基因甲基化与表达之间的简单相关性。这一结果与之前关于肿瘤细胞中DNA甲基化紊乱的发现一致。

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