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Impaired fear response in mice lacking GIT1
Authors:Robert Schmalzigaug  Ramona M. Rodriguiz  Pamela E. Bonner  Collin E. Davidson  William C. Wetsel  Richard T. Premont
Affiliation:1. Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA;2. Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC 27710, USA;3. Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA;4. Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA;5. Mouse Behavioral and Neuroendocrine Analysis Core Facility, Duke University Medical Center, Durham, NC 27710, USA
Abstract:G protein-coupled receptor kinase interacting protein 1 (GIT1) belongs to the family of Arf GAP proteins and has been implicated in the regulation of G protein-coupled receptor (GPCR) sequestration, cell migration, synapse formation and dendritic spine morphogenesis in neurons. To extend these cellular studies on GIT1 to an in vivo system, we generated mice with globally inactivated Git1 gene by breeding mice carrying a conditional Git1flox allele with mice expressing the CMV-Cre transgene. Although many GIT1 knockout (GIT1-KO) animals died shortly after birth, homozygous mutants that survived the early post-partum period developed normally into adulthood and were fertile. Behavioral analyses of adult GIT1-KO mice revealed normal exploratory, anxiety- and depressive-like behaviors. However, GIT1-KO mice show impaired responses to fear conditioning and fear-potentiated startle. Overall, these findings suggest that GIT1 is involved in the regulation of amygdala-mediated experience-based emotional behaviors.
Keywords:GIT1   GIT2   Knockout mice   Behavior   Fear conditioning
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