Behavioral and neuroanatomical characterization of the Fmr1 knockout mouse
Version of Record online: 29 JAN 2002
Copyright © 2002 Wiley-Liss, Inc.
Special Issue: Gene Targeting and Hippocampal Function
Volume 12, Issue 1, pages 39–46, 2002
How to Cite
Mineur, Y. S., Sluyter, F., de Wit, S., Oostra, B. A. and Crusio, W. E. (2002), Behavioral and neuroanatomical characterization of the Fmr1 knockout mouse. Hippocampus, 12: 39–46. doi: 10.1002/hipo.10005
- Issue online: 29 JAN 2002
- Version of Record online: 29 JAN 2002
- Manuscript Accepted: 1 AUG 2001
- Earth and Life Sciences Foundation, Netherlands Organization for Scientific Research. Grant Number: PULS Grant 48.001
- National Institutes of Health. Grant Number: 5 RO1 HD38038
- mossy fiber;
- locomotor activity;
- radial maze learning;
Previous studies showed the Fmr1 knockout (KO) mouse to be an excellent animal model for human fragile-X syndrome. The aim of this study was to further characterize the phenotype of these animals. Neuroanatomically, KO male mice were compared to wild-types (littermates) with respect to their sizes of hippocampal intra- and infrapyramidal mossy fiber (IIPMF) terminal fields. Behaviorally, they were tested in four different paradigms, each measuring different aspects of cognitive and emotional behavior: elevated plus maze (anxiety), neutral cage (aggression), open field (exploration), and radial maze (spatial memory). The results showed a diminished ability for radial maze learning associated with smaller sizes of IIPMF terminal fields. In addition, Fmr1 knockout animals exhibited increased locomotor activity, while no differences were found for aggression and anxiety. These data suggest the involvement of FMRP protein in the development of spatial learning and the sprouting of IIPMF terminal fields. Hippocampus 2002;12:39–46. © 2002 Wiley-Liss, Inc.