Warren W, Crathorn A R, Shooter K V
Biochim Biophys Acta. 1979 Jun 20;563(1):82-8. doi: 10.1016/0005-2787(79)90009-1.
V79-379A cells growing in suspension culture were treated with N-methyl-N-nitrosourea at concentrations of 0.6 and 1.2 mM. After incubation for periods from 1 to 48 h DNA was isolated from the cells and the concentrations of 7-methylguanine, O6-methylguanine, 3-methyladenine and methyl phosphotriesters were determined. After correction for dilution resulting from DNA synthesis during the incubation it was found that no loss of O6-methylguanine or methylphosphotriesters occurred; 7-methylguanine disappeared with a half-life of 22 h and 3-methyladenine was detectable only immediately after the initial treatment. The results show that these cells eliminate 7-methylguanine and 3-methyladenine from DNA by a repair process but are unable to excise or repair O6-methylguanine or methyl phosphotriesters.
悬浮培养的V79 - 379A细胞用浓度为0.6和1.2 mM的N - 甲基 - N - 亚硝基脲处理。孵育1至48小时后,从细胞中分离DNA,并测定7 - 甲基鸟嘌呤、O6 - 甲基鸟嘌呤、3 - 甲基腺嘌呤和甲基磷酸三酯的浓度。校正孵育期间DNA合成导致的稀释后,发现O6 - 甲基鸟嘌呤或甲基磷酸三酯没有损失;7 - 甲基鸟嘌呤以22小时的半衰期消失,3 - 甲基腺嘌呤仅在初始处理后立即可检测到。结果表明,这些细胞通过修复过程从DNA中消除7 - 甲基鸟嘌呤和3 - 甲基腺嘌呤,但无法切除或修复O6 - 甲基鸟嘌呤或甲基磷酸三酯。