Robarts Research Institute and Department of Biochemistry, Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario N6A 5B7, Canada.
Robarts Research Institute and Department of Biochemistry, Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario N6A 5B7, Canada.
Mutat Res Rev Mutat Res. 2015 Jan-Mar;763:15-29. doi: 10.1016/j.mrrev.2014.06.002. Epub 2014 Jul 4.
Ku is an abundant, highly conserved DNA binding protein found in both prokaryotes and eukaryotes that plays essential roles in the maintenance of genome integrity. In eukaryotes, Ku is a heterodimer comprised of two subunits, Ku70 and Ku80, that is best characterized for its central role as the initial DNA end binding factor in the "classical" non-homologous end joining (C-NHEJ) pathway, the main DNA double-strand break (DSB) repair pathway in mammals. Ku binds double-stranded DNA ends with high affinity in a sequence-independent manner through a central ring formed by the intertwined strands of the Ku70 and Ku80 subunits. At the break, Ku directly and indirectly interacts with several C-NHEJ factors and processing enzymes, serving as the scaffold for the entire DNA repair complex. There is also evidence that Ku is involved in signaling to the DNA damage response (DDR) machinery to modulate the activation of cell cycle checkpoints and the activation of apoptosis. Interestingly, Ku is also associated with telomeres, where, paradoxically to its DNA end-joining functions, it protects the telomere ends from being recognized as DSBs, thereby preventing their recombination and degradation. Ku, together with the silent information regulator (Sir) complex is also required for transcriptional silencing through telomere position effect (TPE). How Ku associates with telomeres, whether it is through direct DNA binding, or through protein-protein interactions with other telomere bound factors remains to be determined. Ku is central to the protection of organisms through its participation in C-NHEJ to repair DSBs generated during V(D)J recombination, a process that is indispensable for the establishment of the immune response. Ku also functions to prevent tumorigenesis and senescence since Ku-deficient mice show increased cancer incidence and early onset of aging. Overall, Ku function is critical to the maintenance of genomic integrity and to proper cellular and organismal development.
Ku 是一种在原核生物和真核生物中都丰富存在的高度保守的 DNA 结合蛋白,在维持基因组完整性方面发挥着重要作用。在真核生物中,Ku 是由两个亚基 Ku70 和 Ku80 组成的异源二聚体,其特征在于它作为“经典”非同源末端连接(C-NHEJ)途径中最初的 DNA 末端结合因子的核心作用,该途径是哺乳动物中主要的 DNA 双链断裂(DSB)修复途径。Ku 通过由 Ku70 和 Ku80 亚基交织的链形成的中央环,以序列非依赖性的方式与双链 DNA 末端高亲和力结合。在断裂处,Ku 直接和间接与几种 C-NHEJ 因子和加工酶相互作用,作为整个 DNA 修复复合物的支架。也有证据表明 Ku 参与信号转导至 DNA 损伤反应(DDR)机制,以调节细胞周期检查点的激活和细胞凋亡的激活。有趣的是,Ku 也与端粒相关联,与它的 DNA 末端连接功能相反,它保护端粒末端不被识别为 DSB,从而防止它们的重组和降解。Ku 与沉默信息调节剂(Sir)复合物一起,也需要通过端粒位置效应(TPE)来实现转录沉默。Ku 如何与端粒相关联,是通过直接 DNA 结合,还是通过与其他与端粒结合的因子的蛋白质-蛋白质相互作用,仍有待确定。Ku 通过参与 C-NHEJ 修复 V(D)J 重组过程中产生的 DSB,对保护生物体至关重要,该过程对于建立免疫反应是不可或缺的。Ku 还具有预防肿瘤发生和衰老的作用,因为 Ku 缺陷小鼠显示出癌症发病率增加和衰老提前。总的来说,Ku 功能对于维持基因组完整性以及适当的细胞和机体发育至关重要。