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A transposase-derived gene required for human brain development.
Zapater, Luz Jubierre; Rodriguez-Fos, Elias; Planas-Felix, Merce; Lewis, Sara; Cameron, Daniel; Demarest, Phillip; Nabila, Anika; Zhao, Junfei; Bergin, Paul; Reed, Casie; Yamada, Makiko; Pagnozzi, Alex; Nava, Caroline; Bourel-Ponchel, Emilie; Neilson, Derek E; Dursun, Ali; Özgül, R Köksal; Akar, Halil Tuna; Socci, Nicholas D; Hayes, Matthew; Rabadan, Raul; Torrents, David; Kruer, Michael C; Toth, Miklos; Kentsis, Alex.
Afiliación
  • Zapater LJ; Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10021.
  • Rodriguez-Fos E; Tow Center for Developmental Oncology, Department of Pediatrics, Memorial Sloan Kettering Cancer Center; New York, United States, 10021.
  • Planas-Felix M; Barcelona Supercomputing Center (BSC), Barcelona, Spain, 08034.
  • Lewis S; Barcelona Supercomputing Center (BSC), Barcelona, Spain, 08034.
  • Cameron D; Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital and Departments of Child Health, Neurology, Genetics and Cellular & Molecular Medicine, Phoenix, AZ.
  • Demarest P; Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10021.
  • Nabila A; Tow Center for Developmental Oncology, Department of Pediatrics, Memorial Sloan Kettering Cancer Center; New York, United States, 10021.
  • Zhao J; Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10021.
  • Bergin P; Department of Pharmacology, Weill Cornell Medical College, New York, NY, 10021.
  • Reed C; Program for Mathematical Genomics, Departments of Systems Biology and Biomedical Informatics, Columbia University, New York, NY.
  • Yamada M; Department of Pharmacology, Weill Cornell Medical College, New York, NY, 10021.
  • Pagnozzi A; Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10021.
  • Nava C; Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10021.
  • Bourel-Ponchel E; Tow Center for Developmental Oncology, Department of Pediatrics, Memorial Sloan Kettering Cancer Center; New York, United States, 10021.
  • Neilson DE; CSIRO Health and Biosecurity, The Australian e-Health Research Centre, Brisbane, Australia.
  • Dursun A; Assistance Publique-Hôpitaux de Paris, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.
  • Özgül RK; Research Group on Multimodal Analysis of Brain Function, University of Picardie Jules Verne, France.
  • Akar HT; Pediatric Neurophysiology Unit, Amiens Picardie University Hospital, France.
  • Socci ND; Phoenix Children's Hospital, Phoenix, Arizona.
  • Hayes M; Hacettepe University, Faculty of Medicine & Institute of Child Health, Department of Pediatric Metabolism, Ankara, Turkey.
  • Rabadan R; Hacettepe University, Faculty of Medicine & Institute of Child Health, Department of Pediatric Metabolism, Ankara, Turkey.
  • Torrents D; Hacettepe University, Faculty of Medicine & Institute of Child Health, Department of Pediatric Metabolism, Ankara, Turkey.
  • Kruer MC; Molecular Pharmacology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10021.
  • Toth M; Department of Physics and Computer Science, Xavier University of Louisiana, New Orleans, LA.
  • Kentsis A; Program for Mathematical Genomics, Departments of Systems Biology and Biomedical Informatics, Columbia University, New York, NY.
bioRxiv ; 2023 May 23.
Article en En | MEDLINE | ID: mdl-37163102
ABSTRACT
DNA transposable elements and transposase-derived genes are present in most living organisms, including vertebrates, but their function is largely unknown. PiggyBac Transposable Element Derived 5 (PGBD5) is an evolutionarily conserved vertebrate DNA transposase-derived gene with retained nuclease activity in cells. Vertebrate brain development is known to be associated with prominent neuronal cell death and DNA breaks, but their causes and functions are not well understood. Here, we show that PGBD5 contributes to normal brain development in mice and humans, where its deficiency causes disorder of intellectual disability, movement and seizures. In mice, Pgbd5 is required for the developmental induction of post-mitotic DNA breaks and recurrent somatic genome rearrangements in neurons. Together, these studies nominate PGBD5 as the long-hypothesized neuronal DNA nuclease required for brain function in mammals.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2023 Tipo del documento: Article