Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice

Go Suzuki, Kathryn M. Harper, Takeshi Hiramoto, Takehito Sawamura, Moonsook Lee, Gina Kang, Kenji Tanigaki, Mahalah Buell, Mark A. Geyer, William S. Trimble, Soh Agatsuma, Noboru Hiroi

Research output: Contribution to journalArticlepeer-review

63 Scopus citations


Deletion or duplication of the human chromosome 22q11.2 is associated with many behavioral traits and neuropsychiatric disorders, including autism spectrum disorders and schizophrenia. However, why phenotypes vary widely among individuals with identical deletions or duplications of 22q11.2 and which specific 22q11.2 genes contribute to these phenotypes are still poorly understood. Previous studies have identified a ∼200 kb 22q11.2 region that contributes to behavioral phenotypes in mice. We tested the role of Septin 5 (Sept5), a gene encoded in the ∼200 kb region, in affective behaviors, cognitive capacities and motor activity. To evaluate the impact of genetic backgrounds on behavioral phenotypes of Sept5 deficiency, we used mice on two genetic backgrounds. Our data show that Sept5 deficiency decreased affiliative active social interaction, but this phenotypic expression was influenced by genetic backgrounds. In contrast, Sept5 deficiency decreased anxiety-related behavior, increased prepulse inhibition and delayed acquisition of rewarded goal approach, independent of genetic background. These data suggest that Sept5 deficiency exerts pleiotropic effects on a select set of affective behaviors and cognitive processes and that genetic backgrounds could provide an epistatic influence on phenotypic expression.

Original languageEnglish (US)
Pages (from-to)1652-1660
Number of pages9
JournalHuman molecular genetics
Issue number9
StatePublished - 2009
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)


Dive into the research topics of 'Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice'. Together they form a unique fingerprint.

Cite this