| Project/Area Number |
18602006
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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 |
食の安全
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| Research Institution | National Institute of Health Sciences |
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Principal Investigator |
KIKUCHI Yutaka National Institute of Health Sciences, Division of Microbiology, Researcher (10234197)
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| Project Period (FY) |
2006 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
|
| Budget Amount *help |
¥4,240,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥540,000)
Fiscal Year 2007: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Fiscal Year 2006: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | prion / alternative splicing / GPI-anchor / hypoxia / 選択的スプライシング / スプライシング |
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| Research Abstract |
The human prion protein (PrP) is a glycoprotein with a glycasylphosphatidylinositol (GPI) anchor at its C-terminus. Here I report alternative splicing within exon 2 of the PrP gene (PRNP) in the human glioblastoma cell line T98G. An open reading frame of the alternatively spliced mRNA lacked the GPI anchor signal sequence and encoded a 230-amino acid polypeptide. Its product, GPI-anchorless PrP (GPI^-PrPSV), was unglycosylated and nonionic detergent-soluble and was found in the cytosolic fraction. I also detected low levels of alternatively spliced mRNA in human brain and non-neuronal tissues. On the other hand, I find alternative splicing within exon 3 of the PrP gene in the bovine cornea cell line BCE C/D-lb. The open reading frame of the bovine alternatively spliced mRNA lacked the GPI anchor signal sequence and encoded a 260-amino acid polypeptide. When long-term passaged T98G cells were placed in a low-oxygen environment, alternatively spliced mRNA expression increased while ordinary PrP mRNA expression decreased. These findings imply that oxygen tensions regulate GPI^-PrPSV expression in T98G cells.
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