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Mechanism and Regulation of DNA-Protein Crosslink Repair by the DNA-Dependent Metalloprotease SPRTN.
Stingele, Julian; Bellelli, Roberto; Alte, Ferdinand; Hewitt, Graeme; Sarek, Grzegorz; Maslen, Sarah L; Tsutakawa, Susan E; Borg, Annabel; Kjær, Svend; Tainer, John A; Skehel, J Mark; Groll, Michael; Boulton, Simon J.
Afiliación
  • Stingele J; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
  • Bellelli R; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
  • Alte F; Center for Integrated Protein Science at the Department Chemie, Lehrstuhl für Biochemie, Technische Universität München, Lichtenbergstrasse 4, 85747 Garching, Germany.
  • Hewitt G; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
  • Sarek G; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
  • Maslen SL; MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK.
  • Tsutakawa SE; Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
  • Borg A; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
  • Kjær S; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
  • Tainer JA; Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA; Department of Molecular and Cellular Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
  • Skehel JM; MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK.
  • Groll M; Center for Integrated Protein Science at the Department Chemie, Lehrstuhl für Biochemie, Technische Universität München, Lichtenbergstrasse 4, 85747 Garching, Germany.
  • Boulton SJ; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. Electronic address: simon.boulton@crick.ac.uk.
Mol Cell ; 64(4): 688-703, 2016 11 17.
Article en En | MEDLINE | ID: mdl-27871365
Covalent DNA-protein crosslinks (DPCs) are toxic DNA lesions that interfere with essential chromatin transactions, such as replication and transcription. Little was known about DPC-specific repair mechanisms until the recent identification of a DPC-processing protease in yeast. The existence of a DPC protease in higher eukaryotes is inferred from data in Xenopus laevis egg extracts, but its identity remains elusive. Here we identify the metalloprotease SPRTN as the DPC protease acting in metazoans. Loss of SPRTN results in failure to repair DPCs and hypersensitivity to DPC-inducing agents. SPRTN accomplishes DPC processing through a unique DNA-induced protease activity, which is controlled by several sophisticated regulatory mechanisms. Cellular, biochemical, and structural studies define a DNA switch triggering its protease activity, a ubiquitin switch controlling SPRTN chromatin accessibility, and regulatory autocatalytic cleavage. Our data also provide a molecular explanation on how SPRTN deficiency causes the premature aging and cancer predisposition disorder Ruijs-Aalfs syndrome.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Proteínas de Schizosaccharomyces pombe / Proteínas de Caenorhabditis elegans / Proteínas de Unión al ADN / Reparación del ADN / Proteína de la Xerodermia Pigmentosa del Grupo A Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Proteínas de Schizosaccharomyces pombe / Proteínas de Caenorhabditis elegans / Proteínas de Unión al ADN / Reparación del ADN / Proteína de la Xerodermia Pigmentosa del Grupo A Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article
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