MacLeod A R, Rouleau J, Szyf M
Department of Pharmacology and Therapeutics, McGill University, Montreal, PQ Canada.
J Biol Chem. 1995 May 12;270(19):11327-37. doi: 10.1074/jbc.270.19.11327.
We demonstrate that DNA methylation in an adrenocortical tumor cell line, Y1, is controlled by the Ras signaling pathway. Forced expression of a cDNA encoding human GAP120 (hGAP), a down-modulator of Ras activity or delta 9-Jun a transdominant negative mutant of Jun, in Y1 cells reverts the transformed morphology of the cells and results in a reduction in the level of DNA methylation, DNA methyltransferase (MeTase) mRNA, and enzymatic activity. Introduction of an oncogenic Ha-ras into the GAP transfectants results in reversion to a transformed morphology and an increase in the levels of DNA methylation and DNA MeTase activity. Transient transfection CAT assays demonstrate that the expression of DNA MeTase promoter in Y1 cells is regulated by Ras and AP-1. These results establish a molecular link between a major signaling pathway involved in tumorigenesis and DNA methylation.
我们证明,肾上腺皮质肿瘤细胞系Y1中的DNA甲基化受Ras信号通路控制。在Y1细胞中强制表达编码人GAP120(hGAP,一种Ras活性下调因子)的cDNA或δ9-Jun(Jun的反式显性负突变体),可使细胞的转化形态恢复正常,并导致DNA甲基化水平、DNA甲基转移酶(MeTase)mRNA水平及酶活性降低。将致癌性Ha-ras导入GAP转染细胞中会导致细胞形态恢复为转化形态,且DNA甲基化水平和DNA MeTase活性增加。瞬时转染CAT分析表明,Y1细胞中DNA MeTase启动子的表达受Ras和AP-1调控。这些结果在参与肿瘤发生的主要信号通路与DNA甲基化之间建立了分子联系。