Chan S O, Wong S S, Yeung D C
Department of Biochemistry, University of Hong Kong.
Mol Cell Biochem. 1992 Nov 4;117(1):71-9. doi: 10.1007/BF00230412.
Results from nuclear run-off assays show that exposure of hepatocytes and Reuber H35B hepatoma cells to the tumour promoter, 12-O-tetradecanoylphorbol-13-acetate (TPA), leads to enhanced transcription of c-Ki-ras gene. This increase in transcription in turn results in an accumulation of the functionally active c-Ki-ras message. The half life of c-Ki-ras message in both normal and transformed livers cells is not altered by TPA and is determined to be 3.5 hr. The induction of c-Ki-ras message is accompanied by an increase in the level of c-Ki-ras protein.
核转录试验结果表明,将肝细胞和鲁伯H35B肝癌细胞暴露于肿瘤启动子12 - O - 十四烷酰佛波醇-13 - 乙酸酯(TPA)下,会导致c - Ki - ras基因的转录增强。转录的这种增加进而导致功能性活性c - Ki - ras信使核糖核酸的积累。在正常和转化的肝细胞中,c - Ki - ras信使核糖核酸的半衰期不受TPA影响,经测定为3.5小时。c - Ki - ras信使核糖核酸的诱导伴随着c - Ki - ras蛋白水平的增加。