| Literature DB >> 21093492 |
Shannon M Hamilton1, Corinne M Spencer, Wilbur R Harrison, Lisa A Yuva-Paylor, Deanna F Graham, Ray A M Daza, Robert F Hevner, Paul A Overbeek, Richard Paylor.
Abstract
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.Entities:
Mesh:
Year: 2010 PMID: 21093492 PMCID: PMC3022332 DOI: 10.1016/j.bbr.2010.11.026
Source DB: PubMed Journal: Behav Brain Res ISSN: 0166-4328 Impact factor: 3.332