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Publication : Impairment of social behavior and communication in mice lacking the Uba6-dependent ubiquitin activation system.

First Author  Lee JY Year  2015
Journal  Behav Brain Res Volume  281
Pages  78-85 PubMed ID  25523030
Mgi Jnum  J:224069 Mgi Id  MGI:5661162
Doi  10.1016/j.bbr.2014.12.019 Citation  Lee JY, et al. (2015) Impairment of social behavior and communication in mice lacking the Uba6-dependent ubiquitin activation system. Behav Brain Res 281:78-85
abstractText  The Uba6-Use1 ubiquitin enzyme cascade is a poorly understood arm of the ubiquitin-proteasome system required for mouse development. Recently, we reported that Uba6 brain-specific knockout (termed NKO) mice display abnormal social behavior and neuronal development due to a decreased spine density and accumulation of Ube3a and Shank3. To better characterize a potential role for NKO mice in autism spectrum disorders (ASDs), we performed a comprehensive behavioral characterization of the social behavior and communication of NKO mice. Our behavioral results confirmed that NKO mice display social impairments, as indicated by fewer vocalizations and decreased social interaction. We conclude that UBA6 NKO mice represent a novel ASD mouse model of anti-social and less verbal behavioral symptoms.
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