Perry M E, Rolfe M, McIntyre P, Commane M, Stark G R
Department of Molecular Biology, Imperial Cancer Research Fund, Lincoln's Inn Fields, London, Great Britain.
Mutat Res. 1992 May;276(3):189-97. doi: 10.1016/0165-1110(92)90008-w.
Treatment of Syrian hamster kidney cells with the demethylating agent 5-aza-2'-deoxycytidine (azadC) increased both the frequency and the rate of gene amplification appreciably. AzadC caused substantial DNA demethylation, which is likely to be responsible. The magnitude of the increases depended on the concentrations of both azadC and the drug used for selection. A transient stress response is not responsible since the increases were not dependent on cytotoxicity and were still apparent after several weeks. We discuss mechanisms by which azadC treatment may induce amplification by rendering DNA more prone to this process or by increasing the transcription of genes whose protein products stimulate amplification.
用去甲基化剂5-氮杂-2'-脱氧胞苷(azadC)处理叙利亚仓鼠肾细胞,可显著提高基因扩增的频率和速率。AzadC导致了大量的DNA去甲基化,这可能是其原因所在。增加的幅度取决于azadC和用于选择的药物的浓度。短暂的应激反应并非原因,因为增加并不依赖于细胞毒性,并且在数周后仍然明显。我们讨论了azadC处理可能通过使DNA更容易发生这一过程或通过增加其蛋白质产物刺激扩增的基因的转录来诱导扩增的机制。