Multiple autism-like behaviors in a novel transgenic mouse model

被引:40
|
作者
Hamilton, Shannon M. [1 ]
Spencer, Corinne M. [2 ]
Harrison, Wilbur R. [1 ,3 ]
Yuva-Paylor, Lisa A. [2 ]
Graham, Deanna F. [2 ]
Daza, Ray A. M. [4 ]
Hevner, Robert F. [4 ,5 ]
Overbeek, Paul A. [3 ]
Paylor, Richard [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[4] Seattle Childrens Res Inst, Ctr Integrat Brain Res, Seattle, WA 98101 USA
[5] Univ Washington, Sch Med, Dept Neurol Surg, Seattle, WA 98104 USA
关键词
Social behavior; Mouse model; Ultrasonic vocalization; Autism; Gene expression; ABNORMAL SOCIAL BEHAVIORS; GENE-EXPRESSION; TASKS RELEVANT; KNOCKOUT MICE; CHILDREN; IDENTIFICATION; AGGRESSION; PHENOTYPES; MUTATION; TWIN;
D O I
10.1016/j.bbr.2010.11.026
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Autism spectrum disorder (ASD) diagnoses are behaviorally based with no defined universal biomarkers, occur at a 1:110 ratio in the population, and predominantly affect males compared to females at approximately a 4:1 ratio. One approach to investigate and identify causes of ASD is to use organisms that display abnormal behavioral responses that model ASD-related impairments. This study describes a novel transgenic mouse, MALTT, which was generated using a forward genetics approach. It was determined that the transgene integrated within a non-coding region on the X chromosome. The MALTT line exhibited a complete repertoire of ASD-like behavioral deficits in all three domains required for an ASD diagnosis: reciprocal social interaction, communication, and repetitive or inflexible behaviors. Specifically, MALTT male mice showed deficits in social interaction and interest, abnormalities in pup and juvenile ultrasonic vocalization communications, and exhibited a repetitive stereotypy. Abnormalities were also observed in the domain of sensory function, a secondary phenotype prevalently associated with ASD. Mapping and expression studies suggested that the Fam46 gene family may be linked to the observed ASD-related behaviors. The MALTT line provides a unique genetic model for examining the underlying biological mechanisms involved in ASD-related behaviors. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 41
页数:13
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