Chatterjee Surajit, Chaubet Loïc, van den Berg Aafke, Mukhortava Ann, Gulkis Mitch, Çağlayan Melike
bioRxiv. 2024 Mar 29:2024.03.28.587287. doi: 10.1101/2024.03.28.587287.
DNA ligases repair the strand breaks are made continually and naturally throughout the genome, if left unrepaired and allowed to persist, they can lead to genome instability in the forms of lethal double-strand (ds) breaks, deletions, and duplications. DNA ligase 1 (LIG1) joins Okazaki fragments during the replication machinery and seals nicks at the end of most DNA repair pathways. Yet, how LIG1 recognizes its target substrate is entirely missing. Here, we uncover the dynamics of nick DNA binding by LIG1 at the single-molecule level. Our findings reveal that LIG1 binds to dsDNA both specifically and non-specifically and exhibits diffusive behavior to form a stable complex at the nick. Furthermore, by comparing with the LIG1 C-terminal protein, we demonstrate that the N-terminal non-catalytic region promotes binding enriched at nick sites and facilitates an efficient nick search process by promoting 1D diffusion along the DNA. Our findings provide a novel single-molecule insight into the nick binding by LIG1, which is critical to repair broken phosphodiester bonds in the DNA backbone to maintain genome integrity.
DNA连接酶修复基因组中持续自然产生的链断裂,如果不进行修复并任其持续存在,它们会以致死性双链(ds)断裂、缺失和重复的形式导致基因组不稳定。DNA连接酶1(LIG1)在复制机制中连接冈崎片段,并在大多数DNA修复途径结束时封闭切口。然而,LIG1如何识别其靶底物却完全未知。在这里,我们在单分子水平上揭示了LIG1与切口DNA结合的动力学。我们的研究结果表明,LIG1与双链DNA既有特异性结合也有非特异性结合,并表现出扩散行为以在切口处形成稳定的复合物。此外,通过与LIG1 C末端蛋白比较,我们证明N末端非催化区域促进在切口位点富集的结合,并通过促进沿DNA的一维扩散来促进有效的切口搜索过程。我们的研究结果为LIG1与切口结合提供了新的单分子见解,这对于修复DNA主链中断裂的磷酸二酯键以维持基因组完整性至关重要。