| Project/Area Number |
17300117
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Neurochemistry/Neuropharmacology
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| Research Institution | Tokyo University of Pharmacy and Life Science |
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Principal Investigator |
YANAGI Shigeru Tokyo University of Pharmacy and Life Science, School of Life Sciences, Professor (60252003)
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| Co-Investigator(Kenkyū-buntansha) |
FUKUDA Toshifumi Tokyo University of Pharmacy and Life Sciences, School of Life Sciences, Research Associate (50372313)
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| Project Period (FY) |
2005 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥15,990,000 (Direct Cost: ¥14,700,000、Indirect Cost: ¥1,290,000)
Fiscal Year 2007: ¥5,590,000 (Direct Cost: ¥4,300,000、Indirect Cost: ¥1,290,000)
Fiscal Year 2006: ¥5,000,000 (Direct Cost: ¥5,000,000)
Fiscal Year 2005: ¥5,400,000 (Direct Cost: ¥5,400,000)
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| Keywords | Axon guidance / Semanhorin / Redox signaling / ROS / GTPase CRAG / PML body / Polvglutamine disease / Gene therapy / 脳神経 / 脳神経疾患 |
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| Research Abstract |
Semaphorins play a critical role in axon guidance as repulsive factors and CRMP family proteins are believed to be involved in semaphorin signaling. We have identified a novel GTPase named CRAG containing a nuclear localization signal sequence (NLS) as a binding protein of collapsin response mediator protein (CRMP) -associated molecule (CRAM ICRMP-51) . In neurons, CRAG plays an important role for reactive oxygen species (ROS) -mediated stress response including semaphorin3A signaling. Interestingly, CRAG forms unique nuclear inclusion associated with PML bodies after stimulation of semaphorin3A. This result supports that semaphorins utilize redox signaling and provides new concept that semaphorins may regulate transcriptional regulation in nudes by activation of CRAG.
On the other hand, CRAG was found to be involved in the molecular mechanism of polyglutamine disease. Actually, CRAG associates with and PML, leading to a large ling-like stnicture of PML body with ubiquitination which is characteristic of polyglutamine diseases. Importantly, CRAG promoted a rapid degradation of misfolded polyglutamine proteins in the nuclear inclusions through ubiquitin-proteasome pathway and attenuated their cell toxicity. Most recently, we showed that lentivector-mediated CRAG expression in cerebellar neurons cleared PolyQ aggregates and strikingly ameliorated severe ataxia in model mice of polyglutamine disease.
In the near future, targeted expression of CRAG is a potential gene therapy for human polyglutamine diseases.
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