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lüll A structural model for regulation of NHEJ by DNA-PKcs autophosphorylation Dobbs TA; Tainer JA; Lees-Miller SPDNA Repair (Amst) 2010[Dec]; 9 (12): 1307-14The DNA-dependent protein kinase catalytic subunit (DNA-PKcs) and Ku heterodimer together form the biologically critical DNA-PK complex that plays key roles in the repair of ionizing radiation-induced DNA double-strand breaks through the non-homologous end-joining (NHEJ) pathway. Despite elegant and informative electron microscopy studies, the mechanism by which DNA-PK co-ordinates the initiation of NHEJ has been enigmatic due to limited structural information. Here, we discuss how the recently described small angle X-ray scattering structures of full-length Ku heterodimer and DNA-PKcs in solution, combined with a breakthrough DNA-PKcs crystal structure, provide significant insights into the early stages of NHEJ. Dynamic structural changes associated with a functionally important cluster of autophosphorylation sites play a significant role in regulating the dissociation of DNA-PKcs from Ku and DNA. These new structural insights have implications for understanding the formation and control of the DNA-PK synaptic complex, DNA-PKcs activation and initiation of NHEJ. More generally, they provide prototypic information for the phosphatidylinositol-3 kinase-like (PIKK) family of serine/threonine protein kinases that includes Ataxia Telangiectasia-Mutated (ATM) and ATM-, Rad3-related (ATR) as well as DNA-PKcs.|*DNA Breaks, Double-Stranded[MESH]|*Models, Molecular[MESH]|DNA Helicases/metabolism[MESH]|DNA Repair/genetics/*physiology[MESH]|DNA-Activated Protein Kinase/*metabolism[MESH]|DNA-Binding Proteins/*metabolism[MESH]|Ku Autoantigen[MESH]|Nuclear Proteins/*metabolism[MESH]|Phosphorylation[MESH] |