Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, USA.
Nat Struct Mol Biol. 2023 Jan;30(1):115-124. doi: 10.1038/s41594-022-00871-y. Epub 2023 Jan 2.
Genotoxins cause nascent strand degradation (NSD) and fork reversal during DNA replication. NSD and fork reversal are crucial for genome stability and are exploited by chemotherapeutic approaches. However, it is unclear how NSD and fork reversal are triggered. Additionally, the fate of the replicative helicase during these processes is unknown. We developed a biochemical approach to study synchronous, localized NSD and fork reversal using Xenopus egg extracts and validated this approach with experiments in human cells. We show that replication fork uncoupling stimulates NSD of both nascent strands and progressive conversion of uncoupled forks to reversed forks. Notably, the replicative helicase remains bound during NSD and fork reversal. Unexpectedly, NSD occurs before and after fork reversal, indicating that multiple degradation steps take place. Overall, our data show that uncoupling causes NSD and fork reversal and elucidate key events that precede fork reversal.
遗传毒素在 DNA 复制过程中导致新生链降解 (NSD) 和叉反转。NSD 和叉反转对于基因组稳定性至关重要,并且被化学治疗方法利用。然而,不清楚 NSD 和叉反转是如何触发的。此外,在这些过程中复制解旋酶的命运尚不清楚。我们开发了一种生化方法来使用非洲爪蟾卵提取物研究同步、局部 NSD 和叉反转,并通过在人细胞中的实验验证了这种方法。我们表明,复制叉解偶联刺激新生链的 NSD 以及未偶联叉的逐渐转化为反转叉。值得注意的是,复制解旋酶在 NSD 和叉反转过程中保持结合。出乎意料的是,NSD 发生在叉反转之前和之后,表明发生了多个降解步骤。总体而言,我们的数据表明解偶联导致 NSD 和叉反转,并阐明了叉反转之前的关键事件。