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Cryo-EM visualization of DNA-PKcs structural intermediates in NHEJ.
Chen, Siyu; Vogt, Alex; Lee, Linda; Naila, Tasmin; McKeown, Ryan; Tomkinson, Alan E; Lees-Miller, Susan P; He, Yuan.
Afiliação
  • Chen S; Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
  • Vogt A; Interdisciplinary Biological Sciences Program, Northwestern University. Evanston, IL, USA.
  • Lee L; Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
  • Naila T; Interdisciplinary Biological Sciences Program, Northwestern University. Evanston, IL, USA.
  • McKeown R; Department of Biochemistry and Molecular Biology, Robson DNA Science Centre and Arnie Charbonneau Cancer Institute, University of Calgary, Calgary, Alberta T2N 4N1, Canada.
  • Tomkinson AE; Department of Internal Medicine and Molecular Genetics and Microbiology and the University of New Mexico Comprehensive Cancer Center, University of New Mexico, Albuquerque, NM, USA.
  • Lees-Miller SP; Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
  • He Y; Interdisciplinary Biological Sciences Program, Northwestern University. Evanston, IL, USA.
Sci Adv ; 9(22): eadg2838, 2023 06 02.
Article em En | MEDLINE | ID: mdl-37256947
DNA double-strand breaks (DSBs), one of the most cytotoxic forms of DNA damage, can be repaired by the tightly regulated nonhomologous end joining (NHEJ) machinery (Stinson and Loparo and Zhao et al.). Core NHEJ factors form an initial long-range (LR) synaptic complex that transitions into a DNA-PKcs (DNA-dependent protein kinase, catalytic subunit)-free, short-range state to align the DSB ends (Chen et al.). Using single-particle cryo-electron microscopy, we have visualized three additional key NHEJ complexes representing different transition states, with DNA-PKcs adopting distinct dimeric conformations within each of them. Upon DNA-PKcs autophosphorylation, the LR complex undergoes a substantial conformational change, with both Ku and DNA-PKcs rotating outward to promote DNA break exposure and DNA-PKcs dissociation. We also captured a dimeric state of catalytically inactive DNA-PKcs, which resembles structures of other PIKK (Phosphatidylinositol 3-kinase-related kinase) family kinases, revealing a model of the full regulatory cycle of DNA-PKcs during NHEJ.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Quinase Ativada por DNA / Reparo do DNA por Junção de Extremidades Tipo de estudo: Prognostic_studies Idioma: En Revista: Sci Adv Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Quinase Ativada por DNA / Reparo do DNA por Junção de Extremidades Tipo de estudo: Prognostic_studies Idioma: En Revista: Sci Adv Ano de publicação: 2023 Tipo de documento: Article