D'Ambrosio S M, Setlow R B
Proc Natl Acad Sci U S A. 1976 Jul;73(7):2396-400. doi: 10.1073/pnas.73.7.2396.
Alkaline sedimentation profiles of pulse-labeled DNA from Chinese hamster cells showed that DNA from cells treated with N-acetoxy-acetylaminofluorene or ultraviolet radiation was made in segments smaller than those from untreated cells. Cells treated with a small dose (2.5 muM) of N-acetoxy-acetylaminofluorene or (2.5 J-m-2) 254-nm radiation, several hours before a larger dose (7-10 muM) of N-acetoxy-acetylaminofluorene or 5.0 J.m-2 of 254 nm radiation, also synthesized small DNA after the second dose. However, the rate at which this small DNA was joined together into parental size was appreciably greater than in absence of the small dose. This enhancement of postreplication repair (as a result of the initial small dose) was not observed when cells were incubated with cycloheximide between the two treatments. The results suggest that N-acetoxy-acetylaminofluorene and ultraviolet-damaged DNA from Chinese hamster cells are repaired by similar postreplicative mechanisms that require de novo protein synthesis for enhancement.
中国仓鼠细胞经脉冲标记的DNA的碱性沉降图谱表明,用N - 乙酰氧基 - 乙酰氨基芴或紫外线辐射处理的细胞所产生的DNA片段比未处理细胞的小。在给予较大剂量(7 - 10μM)的N - 乙酰氧基 - 乙酰氨基芴或5.0 J.m-2的254nm辐射前数小时,先用小剂量(2.5μM)的N - 乙酰氧基 - 乙酰氨基芴或(2.5 J.m-2)的254nm辐射处理细胞,在第二次给药后这些细胞也合成了小的DNA。然而,这种小DNA连接成亲本大小的速率明显高于未给予小剂量的情况。当在两次处理之间用环己酰亚胺孵育细胞时,未观察到(由于初始小剂量导致的)复制后修复的这种增强。结果表明,中国仓鼠细胞中N - 乙酰氧基 - 乙酰氨基芴和紫外线损伤的DNA通过类似的复制后机制进行修复,这种机制需要从头合成蛋白质来增强。