| Project/Area Number |
17590611
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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 |
Gastroenterology
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| Research Institution | Yamagata University |
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Principal Investigator |
SAITO Takafumi Yamagata University, Department of Gastroenterology, Associate Professor, 医学部, 助教授 (80250918)
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| Co-Investigator(Kenkyū-buntansha) |
KAWATA Sumio Yamagata University, Department of Gastroenterology, Professor, 医学部, 教授 (90183285)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2005: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | Hepatitis C / host / genetic polymorphism / SNP / susceptibility of infection / cell membrane / cohort / glycosylation / 感染感受性 / 遺伝子多型 / 接合蛋白 / ヘパラン硫酸 / HCV / 感染防御 |
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| Research Abstract |
The outcome of hepatitis C virus (HCV) infection varies among individuals, but the genetic factors involved remain unknown. We have reported the 50 SNPs in 32 genes as candidate genes that influence the susceptibility of infection (BBRC 2004 ; 317 : 335-341). From these candidate genes, we further analyzed the genes coding the adaptor proteins that are essential for viral attachment onto cell surface. The HCV virion has been reported to bind heparan sulfate proteoglycan (HS) on the cell surface in the initial step of infection. In this study, we determined the genetic polymorphisms in NDST3 gene that influence the sulfotransferation of HS, and also found the haplotype of this gene. These genetic variations were closely associated with the natural clearance of HCV in the host. We further analyzed the SNPs of the surrounding genes of genes coding the adaptor proteins, and we determined the genetic polymorphisms of TM7SF2 gene in relation to the natural clearance of HCV. The product of TM7SF2 gene is essential for cholesterol synthesis in the liver. This polymorphism represented a coding SNP. Using siRNA technique, we clarified the suppression of HCV replication in the cells after TM7SF2-siRNA transfection in vitro. Thus the genetic variation of TM7SF2 was shown as an important polymorphism that is linked to replication of HCV in the host.
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