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The essential elements for the noncovalent association of two DNA ends during NHEJ synapsis.
Zhao, Bailin; Watanabe, Go; Morten, Michael J; Reid, Dylan A; Rothenberg, Eli; Lieber, Michael R.
Afiliação
  • Zhao B; Department of Pathology, Department of Biochemistry & Molecular Biology, Department of Molecular Microbiology & Immunology, and Section of Computational & Molecular Biology, USC Norris Comprehensive Cancer Center, University of Southern California Keck School of Medicine, Los Angeles, CA
  • Watanabe G; Department of Pathology, Department of Biochemistry & Molecular Biology, Department of Molecular Microbiology & Immunology, and Section of Computational & Molecular Biology, USC Norris Comprehensive Cancer Center, University of Southern California Keck School of Medicine, Los Angeles, CA
  • Morten MJ; Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY, 10016, USA.
  • Reid DA; Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY, 10016, USA.
  • Rothenberg E; Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY, 10016, USA. eli.rothenberg@nyumc.org.
  • Lieber MR; Department of Pathology, Department of Biochemistry & Molecular Biology, Department of Molecular Microbiology & Immunology, and Section of Computational & Molecular Biology, USC Norris Comprehensive Cancer Center, University of Southern California Keck School of Medicine, Los Angeles, CA
Nat Commun ; 10(1): 3588, 2019 08 09.
Article em En | MEDLINE | ID: mdl-31399561
ABSTRACT
One of the most central questions about the repair of a double-strand DNA break (DSB) concerns how the two free DNA ends are brought together - a step called synapsis. Using single-molecule FRET (smFRET), we show here that both Ku plus XRCC4DNA ligase IV are necessary and sufficient to achieve a flexible synapsis of blunt DNA ends, whereas either alone is not. Addition of XLF causes a transition to a close synaptic state, and maximum efficiency of close synapsis is achieved within 20 min. The promotion of close synapsis by XLF indicates a role that is independent of a filament structure, with action focused at the very ends of each duplex. DNA-PKcs is not required for the formation of either the flexible or close synaptic states. This model explains in biochemical terms the evolutionarily central synaptic role of Ku, X4L4, and XLF in NHEJ for all eukaryotes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quebras de DNA de Cadeia Dupla / Reparo do DNA por Junção de Extremidades Tipo de estudo: Risk_factors_studies Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quebras de DNA de Cadeia Dupla / Reparo do DNA por Junção de Extremidades Tipo de estudo: Risk_factors_studies Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá