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.
| Original language | English |
|---|---|
| Title of host publication | Tandem repeats in genes, proteins, and disease |
| Subtitle of host publication | methods and protocols |
| Editors | Danny M. Hatters, Anthony J. Hannan |
| Place of Publication | New York |
| Publisher | Humana Press Inc. |
| Pages | 95-104 |
| Number of pages | 10 |
| ISBN (Electronic) | 9781627034388 |
| ISBN (Print) | 9781627034371 |
| DOIs | |
| Publication status | Published - 2013 |
| Externally published | Yes |
Publication series
| Name | Methods in Molecular Biology |
|---|---|
| Publisher | Humana Press |
| Volume | 1017 |
| ISSN (Print) | 1064-3745 |
Keywords
- aggression
- autism
- fragile X syndrome
- mouse model