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DNA甲基化不参与增殖细胞核抗原基因表达的生长调节。

DNA methylation is not involved in growth regulation of gene expression of proliferating cell nuclear antigen.

作者信息

Liu Y W, Chang K J, Liu Y C

机构信息

Institute of Life Science, National Tsing-Hua University, Hsin-Chu, Taiwan.

出版信息

Exp Cell Res. 1993 Oct;208(2):479-84. doi: 10.1006/excr.1993.1269.

DOI:10.1006/excr.1993.1269
PMID:7690711
Abstract

Expression of proliferating cell nuclear antigen (PCNA) gene is growth regulated. By Southern blot analysis with restriction enzymes such as HpaII and MspI, no change of DNA methylation state in this gene was detected during rat liver regeneration. There is only one HpaII site located in the promoter region of rat PCNA gene and this HpaII site was found to be demethylated in both normal and regenerating livers. Human hepatoma cell lines Hep G2 and Hep 3B were used to study the relation of PCNA gene expression and the DNA methylation. There are 16 HpaII sites in human PCNA gene, and according to the HpaII and MspI restriction patterns, many of the HpaII sites were methylated in vivo. Upon serum stimulation of quiescent cells, no change of DNA methylation state in the HpaII and HhaI sites was found. Demethylation by the methylation inhibitor, 5-azacytidine, did not affect the expression of PCNA gene in the hepatoma cells. With the human primary fibroblasts, Y2, the demethylation by 5-azacytidine did not seem to change the growth dependence of PCNA gene expression. This is consistent with the observation that the expression of PCNA gene of some cultured cell lines such as CHO.K1, in which the PCNA gene was unmethylated, showed growth dependence. Also, no variation in methylation pattern of PCNA gene was found among the different rat tissues in which the expression of PCNA varies. Therefore, we conclude that DNA methylation is not involved in growth regulation of the PCNA gene expression.

摘要

增殖细胞核抗原(PCNA)基因的表达受生长调节。用诸如HpaII和MspI等限制性内切酶进行Southern印迹分析,未检测到该基因在大鼠肝脏再生过程中DNA甲基化状态的变化。大鼠PCNA基因的启动子区域仅存在一个HpaII位点,并且发现该HpaII位点在正常肝脏和再生肝脏中均未甲基化。用人肝癌细胞系Hep G2和Hep 3B研究PCNA基因表达与DNA甲基化的关系。人PCNA基因中有16个HpaII位点,根据HpaII和MspI的限制性图谱,许多HpaII位点在体内被甲基化。对静止细胞进行血清刺激后,未发现HpaII和HhaI位点的DNA甲基化状态发生变化。甲基化抑制剂5-氮杂胞苷引起的去甲基化不影响肝癌细胞中PCNA基因的表达。对于人原代成纤维细胞Y2,5-氮杂胞苷引起的去甲基化似乎并未改变PCNA基因表达对生长的依赖性。这与一些培养细胞系(如PCNA基因未甲基化的CHO.K1)中PCNA基因表达表现出对生长的依赖性这一观察结果一致。此外,在PCNA表达不同的不同大鼠组织中,未发现PCNA基因甲基化模式存在差异。因此,我们得出结论,DNA甲基化不参与PCNA基因表达的生长调节。

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