Gompers Andrea L, Su-Feher Linda, Ellegood Jacob, Copping Nycole A, Riyadh M Asrafuzzaman, Stradleigh Tyler W, Pride Michael C, Schaffler Melanie D, Wade A Ayanna, Catta-Preta Rinaldo, Zdilar Iva, Louis Shreya, Kaushik Gaurav, Mannion Brandon J, Plajzer-Frick Ingrid, Afzal Veena, Visel Axel, Pennacchio Len A, Dickel Diane E, Lerch Jason P, Crawley Jacqueline N, Zarbalis Konstantinos S, Silverman Jill L, Nord Alex S
Department of Psychiatry and Behavioral Sciences, University of California, Davis, Davis, California, USA.
Department of Neurobiology, Physiology and Behavior, University of California, Davis, Davis, California, USA.
Nat Neurosci. 2017 Aug;20(8):1062-1073. doi: 10.1038/nn.4592. Epub 2017 Jun 26.
The chromatin remodeling gene CHD8 represents a central node in neurodevelopmental gene networks implicated in autism. We examined the impact of germline heterozygous frameshift Chd8 mutation on neurodevelopment in mice. Chd8 mice displayed normal social interactions with no repetitive behaviors but exhibited cognitive impairment correlated with increased regional brain volume, validating that phenotypes of Chd8 mice overlap pathology reported in humans with CHD8 mutations. We applied network analysis to characterize neurodevelopmental gene expression, revealing widespread transcriptional changes in Chd8 mice across pathways disrupted in neurodevelopmental disorders, including neurogenesis, synaptic processes and neuroimmune signaling. We identified a co-expression module with peak expression in early brain development featuring dysregulation of RNA processing, chromatin remodeling and cell-cycle genes enriched for promoter binding by Chd8, and we validated increased neuronal proliferation and developmental splicing perturbation in Chd8 mice. This integrative analysis offers an initial picture of the consequences of Chd8 haploinsufficiency for brain development.
染色质重塑基因CHD8是自闭症相关神经发育基因网络中的一个核心节点。我们研究了种系杂合移码Chd8突变对小鼠神经发育的影响。Chd8小鼠表现出正常的社交互动且无重复行为,但出现了与脑区体积增加相关的认知障碍,证实了Chd8小鼠的表型与人类CHD8突变所报告的病理情况重叠。我们应用网络分析来表征神经发育基因表达,揭示了Chd8小鼠中广泛的转录变化,这些变化涉及神经发育障碍中被破坏的各种通路,包括神经发生、突触过程和神经免疫信号传导。我们鉴定出一个在早期脑发育中表达峰值的共表达模块,其特征是RNA加工、染色质重塑和细胞周期基因失调,这些基因富含Chd8的启动子结合位点,并且我们验证了Chd8小鼠中神经元增殖增加和发育性剪接扰动。这种综合分析提供了Chd8单倍体不足对脑发育影响的初步情况。