Division of Oncology, Department of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Methods Mol Biol. 2022;2444:81-103. doi: 10.1007/978-1-0716-2063-2_6.
Single-stranded DNA gaps are frequent structures that accumulate on newly synthesized DNA under conditions of replication stress. The identification of these single-stranded DNA gaps has been instrumental to uncover the mechanisms that allow the DNA replication machinery to skip intrinsic replication obstacles or DNA lesions. DNA fiber assays provide an essential tool for detecting perturbations in DNA replication fork dynamics genome-wide at single molecule resolution along with identifying the presence of single-stranded gaps when used in combination with S1 nuclease. However, electron microscopy is the only technique allowing the actual visualization and localization of single-stranded DNA gaps on replication forks. This chapter provides a detailed method for visualizing single-stranded DNA gaps at the replication fork by electron microscopy including psoralen cross-linking of cultured mammalian cells, extraction of genomic DNA, and finally enrichment of replication intermediates followed by spreading and platinum rotary shadowing of the DNA onto grids. Discussion on identification and analysis of these gaps as well as on the advantages and disadvantages of electron microscopy relative to the DNA fiber technique is also included.
单链 DNA 缺口是在复制应激条件下新合成的 DNA 上频繁出现的结构。这些单链 DNA 缺口的鉴定对于揭示允许 DNA 复制机制跳过内在复制障碍或 DNA 损伤的机制至关重要。DNA 纤维分析提供了一种重要的工具,可在单分子分辨率下对全基因组的 DNA 复制叉动力学进行检测,当与 S1 核酸酶结合使用时,还可以识别单链缺口的存在。然而,电子显微镜是唯一能够实际观察和定位复制叉上单链 DNA 缺口的技术。本章提供了一种通过电子显微镜可视化复制叉上单链 DNA 缺口的详细方法,包括培养的哺乳动物细胞的补骨脂素交联、基因组 DNA 的提取,以及复制中间体的富集,然后将 DNA 铺展到网格上并用铂旋转阴影化。还讨论了这些缺口的鉴定和分析,以及电子显微镜相对于 DNA 纤维技术的优缺点。