Li Huaixing, Shi Ke, Chen Ruiwen, He Yan, Wu Dan, Sun Shuhan
Department of Medical Genetics, Division of Basic Medical Sciences, Second Military Medical University, Shanghai, China.
Acta Biochim Biophys Sin (Shanghai). 2007 Mar;39(3):181-6. doi: 10.1111/j.1745-7270.2007.00269.x.
The p53 promoter-based green fluorescent protein (GFP) and luciferase reporter gene assays have been established for detecting DNA damage induced by genotoxic agents. To evaluate the system, NIH3T3 cells transfected with either pHP53-GFP or pMP53-GFP construct were treated with mitomycin or 5-fluorouracil. Expression of the GFP reporter gene was significantly and specifically induced in the cells exposed to mitomycin or 5-fluorouracil. Then we treated NIH3T3 cells harboring pHP53-Luc or pMP53-Luc vector with mitomycin, 5-fluorouracil or cisplatin at various concentrations. Similarly, exposure of the cells to these agents with genotoxic potentials resulted in a dose-dependent induction in luciferase reporter gene expression. Thus, these in vitro reporter gene assays could provide an ideal system for quick assessment or screening of agents with genotoxic potential.
基于p53启动子的绿色荧光蛋白(GFP)和荧光素酶报告基因检测方法已被用于检测遗传毒性剂诱导的DNA损伤。为了评估该系统,用丝裂霉素或5-氟尿嘧啶处理转染了pHP53-GFP或pMP53-GFP构建体的NIH3T3细胞。在暴露于丝裂霉素或5-氟尿嘧啶的细胞中,GFP报告基因的表达被显著且特异性地诱导。然后,我们用不同浓度的丝裂霉素、5-氟尿嘧啶或顺铂处理携带pHP53-Luc或pMP53-Luc载体的NIH3T3细胞。同样,将细胞暴露于这些具有遗传毒性的试剂中会导致荧光素酶报告基因表达呈剂量依赖性诱导。因此,这些体外报告基因检测方法可为快速评估或筛选具有遗传毒性潜力的试剂提供理想的系统。