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Ku80 C 末端区域与 DNA 依赖性蛋白激酶催化亚基(DNA-PKcs)相互作用的 DNA 要求。

DNA requirements for interaction of the C-terminal region of Ku80 with the DNA-dependent protein kinase catalytic subunit (DNA-PKcs).

作者信息

Radhakrishnan Sarvan Kumar, Lees-Miller Susan P

机构信息

Department of Biochemistry and Molecular Biology, Robson DNA Science Centre, University of Calgary, 3330 Hospital Drive NW, Alberta, T2N 1N4, Canada.

Department of Biochemistry and Molecular Biology, Robson DNA Science Centre, University of Calgary, 3330 Hospital Drive NW, Alberta, T2N 1N4, Canada.

出版信息

DNA Repair (Amst). 2017 Sep;57:17-28. doi: 10.1016/j.dnarep.2017.06.001. Epub 2017 Jun 9.

Abstract

Non-homologous end joining (NHEJ) is the major pathway for the repair of ionizing radiation induced DNA double strand breaks (DSBs) in human cells. Critical to NHEJ is the DNA-dependent interaction of the Ku70/80 heterodimer with the DNA-dependent protein kinase catalytic subunit (DNA-PKcs) to form the DNA-PK holoenzyme. However, precisely how Ku recruits DNA-PKcs to DSBs ends to enhance its kinase activity has remained enigmatic, with contradictory findings reported in the literature. Here we address the role of the Ku80 C-terminal region (CTR) in the DNA-dependent interaction of Ku70/80 with DNA-PKcs using purified components and defined DNA structures. Our results show that the Ku80 CTR is required for interaction with DNA-PKcs on short segments of blunt ended 25bp dsDNA or 25bp dsDNA with a 15-base poly dA single stranded (ss) DNA extension, but this requirement is less stringent on longer dsDNA molecules (35bp blunt ended dsDNA) or 25bp duplex DNA with either a 15-base poly dT or poly dC ssDNA extension. Moreover, the DNA-PKcs-Ku complex preferentially forms on 25 bp DNA with a poly-pyrimidine ssDNA extension.Our work clarifies the role of the Ku80 CTR and dsDNA ends on the interaction of DNA-PKcs with Ku and provides key information to guide assembly and biology of NHEJ complexes.

摘要

非同源末端连接(NHEJ)是人类细胞中修复电离辐射诱导的DNA双链断裂(DSB)的主要途径。NHEJ的关键在于Ku70/80异二聚体与DNA依赖性蛋白激酶催化亚基(DNA-PKcs)的DNA依赖性相互作用,以形成DNA-PK全酶。然而,Ku究竟如何将DNA-PKcs招募到DSB末端以增强其激酶活性仍然是个谜,文献中报道的结果相互矛盾。在这里,我们使用纯化的组分和明确的DNA结构,研究了Ku80 C末端区域(CTR)在Ku70/80与DNA-PKcs的DNA依赖性相互作用中的作用。我们的结果表明,在25bp平端双链DNA或带有15个碱基聚dA单链(ss)DNA延伸的25bp双链DNA的短片段上,Ku80 CTR是与DNA-PKcs相互作用所必需的,但在较长的双链DNA分子(35bp平端双链DNA)或带有15个碱基聚dT或聚dC单链DNA延伸的25bp双链DNA上,这种要求则不那么严格。此外,DNA-PKcs-Ku复合物优先在带有聚嘧啶单链DNA延伸的25bp DNA上形成。我们的工作阐明了Ku80 CTR和双链DNA末端在DNA-PKcs与Ku相互作用中的作用,并为指导NHEJ复合物的组装和生物学提供了关键信息。

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