| Project/Area Number |
11694100
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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 |
Molecular biology
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| Research Institution | Fukuoka Dental College |
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Principal Investigator |
SEKIGUCHI Mutsuo Fukuoka Dental College, Biology, Professor, 歯学部, 教授 (00037342)
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| Co-Investigator(Kenkyū-buntansha) |
SHIMOKAWA Hidetoshi Fukuoka Dental College, Res.Associate, 歯学部, 助手 (50122792)
SANADA Masayuki Fukuoka Dental College, Lecturer, 歯学部, 講師 (40084264)
TAKAGI Yasumitsu Fukuoka Dental College, Assoc.Prof., 歯学部, 助教授 (20212003)
SAKUMI Kunihiko Kyushu Univ.Inst.Med., Res.Associate, 生体防御医学研究所, 助手 (50211933)
HAYAKAWA Hiroshi Kyushu Univ.Sch.Med., Res.Associate, 大学院・医学系研究科, 助手 (70150422)
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| Project Period (FY) |
1999 – 2000
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| Project Status |
Completed (Fiscal Year 2000)
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| Budget Amount *help |
¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 2000: ¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1999: ¥2,100,000 (Direct Cost: ¥2,100,000)
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| Keywords | active oxygen / cancer / mutation / gene targeting / gene cloning / oxidized RNA / E.coli / mouse / 活性酵素 / 細胞株 |
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| Research Abstract |
Oxygen radicals, which can be produced through normal cellular metabolism, play important roles in mutagenesis and carcinogenesis. Among various classes of oxidative DNA damage, 8-oxoguanine (8-oxo-7,8-dihydroguanine) is most important because of its abundance and mutagenicity. The MTH1 gene encodes an enzyme that hydrolyzes 8-oxo-dGTP to monophosphate in the nucleotide pool, thereby preventing occurrence of transversion mutations. By means of gene targeting, we have established MTH1 gene-knockout cell lines and mice. When examined 18 monthe after birth, a greater number of tumors were formed in the lungs, livers and stomachs of MTH1-deficient mice. The MTH1-defient mice will provide a useful model for investigating the role of oxygen radicals in spontaneous carcinogenesis. We also found that the persistence of 8-oxoguanine in messenger RNA causes translational errors. To prevent this outcome, at least two gene products act in Escherichia coli cells. It is of interest to know if similar mechanisms function in mammalian cells.
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