Chagin Vadim O, Reinhart Marius, Cardoso M Cristina
Institute of Cytology, Russian Academy of Science, Saint Petersburg, Russia.
Methods Mol Biol. 2015;1300:43-65. doi: 10.1007/978-1-4939-2596-4_3.
Genomic DNA of a eukaryotic cell is replicated once during the S-phase of the cell cycle to precisely maintain the complete genetic information. In the course of S-phase, semiconservative DNA synthesis is sequentially initiated and performed at thousands of discrete patches of the DNA helix termed replicons. At any given moment of S-phase, multiple replicons are active in parallel in different parts of the genome. In the last decades, tools and methods to visualize DNA synthesis inside cells have been developed. Pulse labeling with nucleotides as well as detecting components of the replication machinery yielded an overall picture of multiple discrete sites of active DNA synthesis termed replication foci (RFi) and forming spatiotemporal patterns within the cell nucleus. Recent advances in fluorescence microscopy and digital imaging in combination with computational image analysis allow a comprehensive quantitative analysis of RFi and provide valuable insights into the organization of the genomic DNA replication process and also of the genome itself. In this chapter, we describe in detail protocols for the visualization and quantification of RFi at different levels of optical and physical resolution.
真核细胞的基因组DNA在细胞周期的S期复制一次,以精确维持完整的遗传信息。在S期过程中,半保留DNA合成在DNA螺旋的数千个离散片段(称为复制子)上依次启动并进行。在S期的任何给定时刻,多个复制子在基因组的不同部分并行活跃。在过去几十年中,已经开发出了可视化细胞内DNA合成的工具和方法。用核苷酸进行脉冲标记以及检测复制机制的组成部分,得到了一幅关于活跃DNA合成的多个离散位点(称为复制灶,RFi)的总体图景,这些位点在细胞核内形成时空模式。荧光显微镜和数字成像技术与计算图像分析相结合的最新进展,使得对RFi进行全面的定量分析成为可能,并为基因组DNA复制过程以及基因组本身的组织提供了有价值的见解。在本章中,我们详细描述了在不同光学和物理分辨率水平下可视化和定量RFi的实验方案。