Effects of inhibitors of DNA synthesis and protein synthesis on the rate of DNA synthesis after exposure of mammalian cells to ultraviolet light

T.D. Griffiths , D.B. Dahle, P.J. Meechan, J.G. Carpenter
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引用次数: 7

Abstract

Chinese hamster V-79 cells were treated with metabolic inhibitors of DNA or protein synthesis for various intervals of time after exposure of 3.0 or 5.0 J · m−2. After removal of the metabolic block(s) the rate of DNA synthesis was followed by measuring the incorporation of [14C]thymidine into acid-insoluble material. A 2.5 or 5.0 h incubation with cycloheximide or hydroxyurea was effective in delaying the onset of the recovery in the rate of DNA synthesis that normally becomes evident several hours after exposure to ultraviolet light. By using concentrations of cycloheximide or hydroxyurea that inhibit DNA synthesis by a similar amount (70%), but protein synthesis by vastly different amounts (95% for cycloheximide; 0% for hydroxyurea), it was apparent that the delay in recovery caused by the treatment of the cells with cycloheximide could be accounted for entirely by its inhibitory effect on DNA synthesis. This suggests that the recovery in DNA synthetic rates following exposure of V-79 cells to ultraviolet light does not appear to require de novo protein synthesis, and therefore does not appear to require the involement of an inducible DNA repair process.

DNA合成和蛋白质合成抑制剂对哺乳动物细胞暴露于紫外光后DNA合成速率的影响
在3.0或5.0 J·m−2暴露后,用不同时间间隔的DNA或蛋白质合成代谢抑制剂处理中国仓鼠V-79细胞。去除代谢阻滞后,通过测量[14C]胸腺嘧啶与酸不溶性物质的掺入来跟踪DNA合成速率。用环己亚胺或羟基脲孵育2.5或5.0小时,可有效延缓DNA合成速率恢复的开始,这种恢复通常在紫外线照射数小时后变得明显。通过使用浓度相似的环己亚胺或羟基脲抑制DNA合成(70%),但对蛋白质合成的抑制量却大不相同(环己亚胺95%;(0%为羟基脲),显然,用环己亚胺处理细胞所造成的恢复延迟可以完全由其对DNA合成的抑制作用来解释。这表明,V-79细胞暴露于紫外线后DNA合成率的恢复似乎不需要从头合成蛋白质,因此似乎不需要诱导DNA修复过程的参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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