| Project/Area Number |
09680803
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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 |
Neuroscience in general
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| Research Institution | Tokyo Metropolitan Institute for Neuroscience (1998)
Okazaki National Research Institutes (1997) |
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Principal Investigator |
KOIKE Satoshi Tokyo Metropolitan Institute for Neuroscience Department of Microbiology and Immunology, Research Scientist, 微生物学・免疫学研究部門, 副参事研究員 (30195630)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 1998: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1997: ¥2,100,000 (Direct Cost: ¥2,100,000)
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| Keywords | cerebral cortex / fuctional area |
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| Research Abstract |
Cerebral cortex of mammals is devided into seraval fuctional areas such as motor, visual, and orditory ares. Each areas are characterized with specific cytoarchtetures and neuroal connections. To investigate the structural and fuctional difference at the molecular level, we attempted to isolate genes which is expressed in a specific area of the cerebral cortex of the old-world monkey, Macaca fascicularis. Two areas, primary motor cortex (area 4 of Broadmann) and primary visual cortex (area 17 of Broadmann) are examined since the difference of the two areas are the biggest as judged by the cytoarchtechture. Poly (A) RNAs are prepared from these areas. Two approach 1) supression subtractive hybridization (SSH : Diachenko et al. (1996) PNAS 93 : 6025-6030)and 2) serial anaylisis of gene expression (SAGE : Velculescu et al. (1995) Science 270 : 484-487) were employed.
1) SSH : We have succeded in several preliminary conditioning experiments using mouse brain and mouse skeltal muscle. It was possible to isolate brain-specific and muscle-specific genes. However, monkey genes expressing in a area-specific mannar were not isolated.
2) SAGE : We have sequenced about 1,500 tags from area 4 and 17. In order to obtain reliable data, we need to sequence ten times more tags. However, there are some technical problems to continue this methods. Technical improvements are required to continue this approach.
Conclusion : It was not possible to isolate genes which are expressed in some specific area of the cerebral cortex using the two methods above. The difference of gene expression pattern between the two regions may be too small to analyze wiith the methods above. New approach such as differential display may be needed to isolate such genes.
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