Windhofer Frank, Wu Wenqi, Iliakis George
Institute of Medical Radiation Biology, University Duisburg-Essen Medical School, Essen, Germany.
J Cell Physiol. 2007 Nov;213(2):475-83. doi: 10.1002/jcp.21120.
Cells of higher eukaryotes rejoin double strand breaks (DSBs) in their DNA predominantly by a non-homologous DNA end joining (NHEJ) pathway that utilizes the products of DNA-PKcs, Ku, LIG4, XRCC4, XLF/Cernunnos, Artemis as well as DNA polymerase lambda (termed D-NHEJ). Mutants with defects in these proteins remove a large proportion of DSBs from their genome utilizing an alternative pathway of NHEJ that operates as a backup (B-NHEJ). While D-NHEJ relies exclusively on DNA ligase IV, recent work points to DNA ligase III as a component of B-NHEJ. Here, we use RNA interference (RNAi) to further investigate the activity requirements for DNA ligase III and IV in the pathways of NHEJ. We report that 70-80% knock down of LIG3 expression has no detectable effect on DSB rejoining, either in D-NHEJ proficient cells, or in cells where D-NHEJ has been chemically or genetically compromised. Surprisingly, also LIG4 knock down has no effect on repair proficient cells, but inhibits DSB rejoining in a radiosensitive cell line with a hypomorphic LIG4 mutation that severely compromises its activity. The results suggest that complete coverage for D-NHEJ or B-NHEJ is afforded by very low ligase levels and demonstrate residual end joining by DNA ligase IV in cells of patients with mutations in LIG4.
高等真核生物细胞主要通过非同源DNA末端连接(NHEJ)途径修复其DNA中的双链断裂(DSB),该途径利用DNA-PKcs、Ku、LIG4、XRCC4、XLF/Cernunnos、Artemis以及DNA聚合酶λ的产物(称为D-NHEJ)。这些蛋白质存在缺陷的突变体利用作为备用途径的另一种NHEJ途径(B-NHEJ)从其基因组中去除大部分DSB。虽然D-NHEJ仅依赖于DNA连接酶IV,但最近的研究表明DNA连接酶III是B-NHEJ的一个组成部分。在这里,我们使用RNA干扰(RNAi)进一步研究NHEJ途径中DNA连接酶III和IV的活性要求。我们报告称,在D-NHEJ功能正常的细胞中,或在D-NHEJ已受到化学或基因损伤的细胞中,LIG3表达敲低70-80%对DSB重新连接没有可检测到的影响。令人惊讶的是,LIG4敲低对修复功能正常的细胞也没有影响,但在具有低表达LIG4突变且严重损害其活性的放射敏感细胞系中抑制DSB重新连接。结果表明,极低的连接酶水平即可实现对D-NHEJ或B-NHEJ的完全覆盖,并证明LIG4突变患者细胞中DNA连接酶IV存在残余的末端连接。