Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States.
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States.
Methods Enzymol. 2022;672:317-338. doi: 10.1016/bs.mie.2022.03.017. Epub 2022 Apr 9.
When a replication fork encounters a nick in the parental DNA, the replisome dissociates and the replication fork structure is lost. This outcome is referred to as replication fork "collapse." Collapsed forks can be highly cytotoxic and mutagenic if not appropriately repaired by the cell. However, the events that occur during and after replication fork collapse are unclear. Here, we describe an in vitro system to induce site specific, strand specific replication fork collapse using Xenopus egg extracts, which contain the full set of DNA replication and repair enzymes. We also describe simple assays to monitor the stability of DNA nicks and the different structures formed during replication fork collapse. This methodology permits detailed mechanistic analysis of collapsed forks in vitro.
当复制叉遇到亲本 DNA 中的一个缺口时,复制体解离,复制叉结构丢失。这种结果称为复制叉“崩溃”。如果细胞不能适当修复,崩溃的叉子可能具有高度细胞毒性和致突变性。然而,在复制叉崩溃期间和之后发生的事件尚不清楚。在这里,我们描述了一种使用非洲爪蟾卵提取物诱导特定位置、特定链复制叉崩溃的体外系统,该提取物包含全套 DNA 复制和修复酶。我们还描述了简单的测定法来监测 DNA 切口的稳定性和复制叉崩溃过程中形成的不同结构。这种方法允许在体外对崩溃的叉子进行详细的机制分析。