Liu Lan, Li Jun, Cisneros-Aguirre Metztli, Merkell Arianna, Stark Jeremy M, Gellert Martin, Yang Wei
Laboratory of Molecular Biology, NIDDK, National Institutes of Health, Bethesda, MD, USA.
Department of Cancer Genetics and Epigenetics, Beckman Research Institute of the City of Hope, Duarte, CA, USA.
Nature. 2025 Jun 11. doi: 10.1038/s41586-025-09078-9.
Non-homologous end joining (NHEJ) is the main repair pathway of double-strand DNA breaks in higher eukaryotes. Here we report reconstitution of the final steps of NHEJ and structures of DNA polymerase μ and ligase IV (LIG4) engaged in gap filling and end joining. These reactions take place in a flexible ω-shaped framework composed of XRCC4 and XLF. Two broken DNA ends, each encircled by Ku70-Ku80 internally, are docked onto the ω frame, mediated by LIG4. DNA polymerase and ligase attached to each ω arm repair only one broken strand of a defined polarity; the final steps of NHEJ requires coordination and toggling of a pair of such enzymes. The facilitators XLF and PAXX additively stimulate NHEJ reactions. As DNA-end sensor and protector, LIG4 replaces DNA-PKcs for end joining and bridges the two DNA ends for polymerase to fill remaining gaps. These assemblies present new targets for NHEJ inhibition to enhance efficacy of radiotherapy and accuracy of gene editing.
非同源末端连接(NHEJ)是高等真核生物中双链DNA断裂的主要修复途径。在此,我们报道了NHEJ最后步骤的重建以及参与缺口填充和末端连接的DNA聚合酶μ和连接酶IV(LIG4)的结构。这些反应发生在由XRCC4和XLF组成的灵活的ω形框架中。两条断裂的DNA末端,每条末端内部都被Ku70-Ku80环绕,在LIG4的介导下对接至ω框架上。附着于每个ω臂的DNA聚合酶和连接酶仅修复具有特定极性的一条断裂链;NHEJ的最后步骤需要一对此类酶的协调和切换。促进因子XLF和PAXX可累加地刺激NHEJ反应。作为DNA末端传感器和保护者,LIG4替代DNA-PKcs进行末端连接,并连接两条DNA末端以便聚合酶填补剩余缺口。这些组装体为抑制NHEJ提供了新的靶点,以提高放射治疗的疗效和基因编辑的准确性。