| Project/Area Number |
11660291
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Basic veterinary science/Basic zootechnical science
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| Research Institution | Hokkaido University |
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Principal Investigator |
ONO Etsuro Hokkaido Univ., Inst. Gen. Med., Asso. Prof., 遺伝子病制御研究所, 助教授 (00160903)
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| Co-Investigator(Kenkyū-buntansha) |
TAHARAGUCHI Satoshi Hokkaido Univ., inst. Gen. Med., Inst., 遺伝子病制御研究所, 助手 (30312416)
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| Project Period (FY) |
1999 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥3,800,000 (Direct Cost: ¥3,800,000)
Fiscal Year 2001: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2000: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1999: ¥2,500,000 (Direct Cost: ¥2,500,000)
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| Keywords | Transgenic mice / Pseudorables virus / Borna disease virus / Neuropathogenicity / Trasnscription factor |
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| Research Abstract |
To assess the neuropathogenic potentials of transcription factors of neurotropic viruses, we have generated several transgenic mouse lines.
Pseudorabies virus (PRV) infection in animals other than its natural host almost always gives rise to fatal diseases in the central nervous system as a result of infection of peripheral neurons and subsequent to the brain. To study the role of immediate-early protein (IE180) of PRV in neuropathogenicity, we have generated transgenic mouse lines expressing IE180 in a tetracycline-regulated system (Tet-Off System). The transgenic mice showed cerebellar symptoms such as ataxic gait, tremor and motor discoordination. In the transgenic mice, histopathology of the cerebellum was remarkable for a failure of layer formation and reduced cerebellum sizes. Although the IE180 transcripts were detected in all tissues, no histological abnormality was observed in the tissues other than cerebellum. These findings suggest that IE180 affects the cascade of gene expression for development of the murine cerebellum.
Borna disease virus infection causes a spectrum of behavioral deficits. To study the role of p24 of BDV in neuropathogenicity, we have generated transgenic mouse lines expressing p24 in astrocytes. The transgenic mice showed enhanced intermale aggressiveness and abnormalities in spatial learning. In the transgenic mice, brain-derived neurotrophic factor and synaptophysin were markedly decreased in hippocampus and cerebellum. These findings suggest that expression and accumulation of p24 in astrocytes creates neurodevelopmental disturbances.
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