Silva Sonia, Gallina Irene, Eckert-Boulet Nadine, Lisby Michael
Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Methods Mol Biol. 2012;920:433-43. doi: 10.1007/978-1-61779-998-3_30.
Fluorescence microscopy of the DNA damage response in living cells stands out from many other DNA repair assays by its ability to monitor the response to individual DNA lesions in single cells. This is particularly true in yeast, where the frequency of spontaneous DNA lesions is relatively low compared to organisms with much larger genomes such as mammalian cells. Single cell analysis of individual DNA lesions allows specific events in the DNA damage response to be correlated with cell morphology, cell cycle phase, and other specific characteristics of a particular cell. Moreover, fluorescence live cell imaging allows for multiple cellular markers to be monitored over several hours. This chapter reviews useful fluorescent markers and genotoxic agents for studying the DNA damage response in living cells and provides protocols for live cell imaging, time-lapse microscopy, and for induction of site-specific DNA lesions.
活细胞中DNA损伤反应的荧光显微镜检查在许多其他DNA修复检测中脱颖而出,因为它能够监测单细胞中对单个DNA损伤的反应。在酵母中尤其如此,与基因组大得多的生物体(如哺乳动物细胞)相比,酵母中自发DNA损伤的频率相对较低。对单个DNA损伤的单细胞分析可以将DNA损伤反应中的特定事件与细胞形态、细胞周期阶段以及特定细胞的其他特定特征联系起来。此外,荧光活细胞成像可以在数小时内监测多个细胞标记物。本章综述了用于研究活细胞中DNA损伤反应的有用荧光标记物和基因毒性剂,并提供了活细胞成像、延时显微镜检查以及诱导位点特异性DNA损伤的实验方案。