Sung Yubin, Kim Chanwoo, Kim Hajin, Takata Kei-Ichi
Center for Genomic Integrity, Institute for Basic Science, Ulsan, Republic of Korea.
Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Methods Mol Biol. 2025;2933:51-67. doi: 10.1007/978-1-0716-4574-1_8.
DNA replication mediated by DNA polymerases is important not only for replicating genomic DNA but also for repairing damaged DNA. Elucidating the function of each DNA polymerase is essential for understanding how genomic integrity is maintained. Here, we present two types of DNA polymerase assays: one is the conventional method using sequence gel and the other is the single-molecule Förster resonance energy transfer (smFRET) measurement. The conventional method is sensitive and suitable for detecting the end product of DNA replication. On the other hand, the smFRET assay can monitor the intermediate stages of the reaction such as the synapsis between two single-stranded DNAs (ssDNAs). The two assays complement each other and provide information for more detailed analysis when used together.
由DNA聚合酶介导的DNA复制不仅对于基因组DNA的复制很重要,而且对于修复受损DNA也很重要。阐明每种DNA聚合酶的功能对于理解基因组完整性如何维持至关重要。在这里,我们介绍两种类型的DNA聚合酶检测方法:一种是使用序列凝胶的传统方法,另一种是单分子荧光共振能量转移(smFRET)测量。传统方法灵敏度高,适用于检测DNA复制的终产物。另一方面,smFRET检测可以监测反应的中间阶段,例如两条单链DNA(ssDNA)之间的突触。这两种检测方法相互补充,一起使用时可为更详细的分析提供信息。