Project/Area Number |
12680753
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Neurochemistry/Neuropharmacology
|
Research Institution | Osaka University |
Principal Investigator |
TAIRA Eiichi Osaka University Graduate School of Medicine, Associate Professor, 医学系研究科, 助教授 (60263240)
|
Co-Investigator(Kenkyū-buntansha) |
TANAKA Hidekazu Osaka University Graduate School of Medicine, Assistant Professor, 医学系研究科, 助手 (70273638)
MIKI Naomasa Osaka University Graduate School of Medicine, Professor, 医学系研究科, 教授 (40094445)
|
Project Period (FY) |
2000 – 2003
|
Project Status |
Completed (Fiscal Year 2003)
|
Budget Amount *help |
¥4,100,000 (Direct Cost: ¥4,100,000)
Fiscal Year 2003: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2002: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2001: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2000: ¥1,800,000 (Direct Cost: ¥1,800,000)
|
Keywords | Cell adhesion molecule / Genomic cloning / Regulation of gene expression / Neurite promotion / 免疫グロブリンスーパーファミリー / 細胞内領域 / 神経突起 / 微絨毛 / 細胞接着 / 海馬 / 脊髄後根神経節 / 細胞骨格 |
Research Abstract |
1) Characterization of gicerin gene We have isolated 16kbp of mouse gicerin gene and determined the sequence. We clarified that the gicerin gene is organized by 16 exons and two isoforms are generated by an alternative splicing of exon 15. Next we determined the promoter region of gicerin gene and determined a responsible domain for growth factor stimulation. The domain was also confirmed by a gel reterdation assay. 2) Analysis of gicerin function in the neurite promotion from PC12 cells. We clarified that increase of gicerin expression in PC 12 cells enhanced neurite promotion. 3) Generation of transgenic mouse, which constitutively express gicerin in nerve cells We established three lines of transgenic mouse, which express gicerin in nerve cells. In order to establish them, we introduced gicerin cDNA with neurofilament promoter as well as GFP with neurofilament promoter.
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