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- Title
Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndrome.
- Authors
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
- Abstract
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. The molecular mechanisms underlying deficits in Down syndrome remain unclear. Here, the authors show that copy number restoration of a chromatin remodeler in trisomic mice is sufficient to rescue epigenomic, physiological and cognitive deficits.
- Subjects
PAPHOS (Cyprus); DOWN syndrome; LABORATORY mice; ANIMAL disease models; INDUCED pluripotent stem cells; FRAGILE X syndrome; ANIMAL rescue
- Publication
Nature Communications, 2022, Vol 13, Issue 1, p1
- ISSN
2041-1723
- Publication type
Article
- DOI
10.1038/s41467-022-34200-0