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Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndrome.
Fulton, Sasha L; Wenderski, Wendy; Lepack, Ashley E; Eagle, Andrew L; Fanutza, Tomas; Bastle, Ryan M; Ramakrishnan, Aarthi; Hays, Emma C; Neal, Arianna; Bendl, Jaroslav; Farrelly, Lorna A; Al-Kachak, Amni; Lyu, Yang; Cetin, Bulent; Chan, Jennifer C; Tran, Tina N; Neve, Rachael L; Roper, Randall J; Brennand, Kristen J; Roussos, Panos; Schimenti, John C; Friedman, Allyson K; Shen, Li; Blitzer, Robert D; Robison, Alfred J; Crabtree, Gerald R; Maze, Ian.
Afiliación
  • Fulton SL; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Wenderski W; Department of Pathology, Stanford Medical School, Palo Alto, CA, 94305, USA.
  • Lepack AE; Department of Genetics, Stanford Medical School, Palo Alto, CA, 94305, USA.
  • Eagle AL; Department of Developmental Biology, Stanford Medical School, Palo Alto, CA, 94305, USA.
  • Fanutza T; Howard Hughes Medical Institute, Stanford University, Palo Alto, CA, 94305, USA.
  • Bastle RM; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Ramakrishnan A; Department of Physiology, Michigan State University, East Lansing, MI, 48824, USA.
  • Hays EC; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Neal A; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Bendl J; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Farrelly LA; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Al-Kachak A; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Lyu Y; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Cetin B; Department of Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Chan JC; Center for Disease Neuroepigenomics, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Tran TN; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Neve RL; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Roper RJ; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Brennand KJ; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Roussos P; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Schimenti JC; Department of Biomedical Sciences, Cornell University, Ithaca, NY, 14853, USA.
  • Friedman AK; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, 14853, USA.
  • Shen L; McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
  • Blitzer RD; Department of Biology, Indiana University-Purdue University, Indianapolis, IN, 46202, USA.
  • Robison AJ; Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Crabtree GR; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
  • Maze I; Department of Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Nat Commun ; 13(1): 6384, 2022 10 26.
Article en En | MEDLINE | ID: mdl-36289231
With an incidence of ~1 in 800 births, Down syndrome (DS) is the most common chromosomal condition linked to intellectual disability worldwide. While the genetic basis of DS has been identified as a triplication of chromosome 21 (HSA21), the genes encoded from HSA21 that directly contribute to cognitive deficits remain incompletely understood. Here, we found that the HSA21-encoded chromatin effector, BRWD1, was upregulated in neurons derived from iPS cells from an individual with Down syndrome and brain of trisomic mice. We showed that selective copy number restoration of Brwd1 in trisomic animals rescued deficits in hippocampal LTP, cognition and gene expression. We demonstrated that Brwd1 tightly binds the BAF chromatin remodeling complex, and that increased Brwd1 expression promotes BAF genomic mistargeting. Importantly, Brwd1 renormalization rescued aberrant BAF localization, along with associated changes in chromatin accessibility and gene expression. These findings establish BRWD1 as a key epigenomic mediator of normal neurodevelopment and an important contributor to DS-related phenotypes.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Down / Trastornos del Conocimiento Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome de Down / Trastornos del Conocimiento Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos