Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits

Bibliographic Details
Title: Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits
Authors: Randall J. Platt, Yang Zhou, Ian M. Slaymaker, Ashwin S. Shetty, Niels R. Weisbach, Jin-Ah Kim, Jitendra Sharma, Mitul Desai, Sabina Sood, Hannah R. Kempton, Gerald R. Crabtree, Guoping Feng, Feng Zhang
Source: Cell Reports, Vol 19, Iss 2, Pp 335-350 (2017)
Publisher Information: Elsevier, 2017.
Publication Year: 2017
Collection: LCC:Biology (General)
Subject Terms: Biology (General), QH301-705.5
More Details: Summary: Autism spectrum disorder (ASD) is a heterogeneous disease, but genetically defined models can provide an entry point to studying the molecular underpinnings of this disorder. We generated germline mutant mice with loss-of-function mutations in Chd8, a de novo mutation strongly associated with ASD, and demonstrate that these mice display hallmark ASD behaviors, macrocephaly, and craniofacial abnormalities similar to patient phenotypes. Chd8+/– mice display a broad, brain-region-specific dysregulation of major regulatory and cellular processes, most notably histone and chromatin modification, mRNA and protein processing, Wnt signaling, and cell-cycle regulation. We also find altered synaptic physiology in medium spiny neurons of the nucleus accumbens. Perturbation of Chd8 in adult mice recapitulates improved acquired motor learning behavior found in Chd8+/– animals, suggesting a role for CHD8 in adult striatal circuits. These results support a mechanism linking chromatin modification to striatal dysfunction and the molecular pathology of ASD. : Platt et al. demonstrate that loss-of-function mutation of the high-confidence ASD-associated gene Chd8 results in behavioral and synaptic defects in mice. Keywords: CRISPR, autism spectrum disorder, MRI, behavior, RNA-seq, ChIP-seq, physiology, neocortical development, adeno-associated virus, Cas9 knockin mouse
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2211-1247
Relation: http://www.sciencedirect.com/science/article/pii/S2211124717303984; https://doaj.org/toc/2211-1247
DOI: 10.1016/j.celrep.2017.03.052
Access URL: https://doaj.org/article/aba3bb6682074342a2b284ec87cc7022
Accession Number: edsdoj.ba3bb6682074342a2b284ec87cc7022
Database: Directory of Open Access Journals
More Details
ISSN:22111247
DOI:10.1016/j.celrep.2017.03.052
Published in:Cell Reports
Language:English