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Characterizing Social Behavior in Genetically Targeted Mouse Models of Brain Disorders

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Part of the book series: Methods in Molecular Biology ((MIMB,volume 1017))

Abstract

Fragile X syndrome, the leading inherited cause of mental retardation and autism spectrum disorders worldwide, is caused by a tandem repeat expansion in the FMR1 (fragile X mental retardation 1) gene. It presents with a distinct behavioral phenotype which overlaps significantly with that of autism. Emerging evidence suggests that tandem repeat polymorphisms (TRPs) might also play a key role in modulating disease susceptibility for a range of common polygenic disorders, including the broader autism spectrum of disorders (ASD) and other forms of psychiatric illness such as schizophrenia, depression, and bipolar disorder [1]. In order to understand how TRPs and associated gene mutations mediate pathogenesis, various mouse models have been generated. A crucial step in such functional genomics is high-quality behavioral and cognitive phenotyping. This chapter presents a basic behavioral battery for standardized tests for assaying social phenotypes in mouse models of brain disorders, with a focus on aggression.

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Acknowledgements

This work was funded by grants to A.J.H. from the National Health and Medical Research Council (APP1034785 and APP1047674). A.J.H. is an Australian Research Council Future Fellow (FT3).

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Burrows, E.L., Hannan, A.J. (2013). Characterizing Social Behavior in Genetically Targeted Mouse Models of Brain Disorders. In: Hatters, D., Hannan, A. (eds) Tandem Repeats in Genes, Proteins, and Disease. Methods in Molecular Biology, vol 1017. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-438-8_7

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  • DOI: https://doi.org/10.1007/978-1-62703-438-8_7

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  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-62703-437-1

  • Online ISBN: 978-1-62703-438-8

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