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The Journal of Neuroscience, December 1, 1999, 19(23):10318-10323

Cerebellar Granule Cell-Specific and Inducible Expression of Cre Recombinase in the Mouse

Mika Tsujita1, Hisashi Mori1, Masahiko Watanabe2, Misao Suzuki3, Jun-ichi Miyazaki4, and Masayoshi Mishina1, 5

1 Department of Molecular Neurobiology and Pharmacology, School of Medicine, University of Tokyo, Tokyo 113-0033, Japan, 2 Department of Anatomy, Hokkaido University, School of Medicine, Sapporo 060-8638, Japan, 3 Center for Animal Resources and Development, Kumamoto University, Kumamoto 860-0811, Japan, 4 Department of Nutrition and Physiological Chemistry, Osaka University Medical School, Osaka 565-0871, Japan, and 5 CREST, Japan Science and Technology Corporation, Saitama 332-0012, Japan

To develop a cell type-specific and temporal regulation system of gene targeting in the cerebellum, we used the NMDA-type glutamate receptor GluRepsilon 3 subunit gene and Cre recombinase-progesterone receptor fusion (CrePR) gene in combination. Injection of the CrePR gene placed under the control of the 10 kb 5' region of the GluRepsilon 3 gene into C57BL/6 eggs yielded the ECP25 line that strongly expressed the CrePR mRNA selectively in the granule cells of the cerebellum. Using a transgenic mouse carrying a reporter gene for Cre-mediated recombination, we showed that antiprogestins could induce the recombinase activity of CrePR protein in the cerebellar granule cells of the ECP25 line. Thus, the established mouse line will provide a valuable tool to investigate the mechanism of cerebellar function by manipulating molecules in the temporally regulated and granule cell-specific manner.

Key words: Cre recombinase; antiprogestin; cerebellum; cerebellar granule cell; gene targeting; NMDA receptor GluRepsilon 3 subunit; progesterone receptor; transgenic mouse


Copyright © 1999 Society for Neuroscience  0270-6474/99/192310318-06$05.00/0


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