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2000 Fiscal Year Final Research Report Summary

Regulatory mechanisms for mutagenesis and carcinogenesis

Research Project

Project/Area Number 11694100
Research Category

Grant-in-Aid for Scientific Research (B).

Allocation TypeSingle-year Grants
Section一般
Research Field Molecular biology
Research InstitutionFukuoka Dental College

Principal Investigator

SEKIGUCHI Mutsuo  Fukuoka Dental College, Biology, Professor, 歯学部, 教授 (00037342)

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)
Project Period (FY) 1999 – 2000
Keywordsactive oxygen / cancer / mutation / gene targeting / gene cloning / oxidized RNA / E.coli / mouse
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.

  • Research Products

    (14 results)

All Other

All Publications (14 results)

  • [Publications] H.Hayakawa: "Metabolic fate of oxidized guanine ribonucleotides in mammalian cells."Biochemistry. 38. 3610-3614 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Oda: "Multi-forms of human MTH1 polypeptides produced by alternative translation initiation and single nucleotide polymorphism."Nucl.Acids Res.. 27. 4335-4343 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Y.Fujii: "Functional significance of the conserved residues for the 23 residue module among MTH1 and MutT family proteins."J.Biol.Chem.. 274. 35251-35259 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Shimokawa: "Functional significance of conserved residues in the phosphohydrolase module of Escherichia coli MutT protein."Nucl.Acids.Res.. 28. 3240-3249 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] A.Shiraishi : "Increased susceptibility of chemotherapeutic alkylating agents of mice deficient in DNA repair methyltransferase"Carcinogenesis. 21. 1879-1883 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Kawate: "A defect in a single allel of the Mlh1 gene causes dissociation of killing and tumorigenic action of an alkylating carcinogen in methyltransferase-deficient mice."Carcinogenesis. 301-305 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Hayakawa, M.Sekiguchi et al.: "Metabolic fate of oxidized guanine ribonucleotides in mammalian cells"Biochemistry. 38. 3610-3614 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H.Oda, M.Sekiguchi et al.: "Multiforms of human MTH1 polypeptides produced by alternative translation initiation and single nucleotide polymorphism"Nucl.Acids Res.. 27. 4335-4343 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Y.Fujii, M.Sekiguchi et al.: "Functional significance of the conserved residues for the 23 residue module among MTH1 and MutT family protein"J.Biol.Chem.. 274. 38251-38259 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] R.Inoue, M.Sekiguchi et al.: "Characterization of human polymorphic O^6-methylguanine-DNA methyltransferase"Phamacogenetics. 10. 59-66 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H.Kawate, M.Sekiguchi et al.: "A defect in a single allele of the Mlh1 gene cuases dissociation of killing and tumorigenic action of alkylating carcinogen in methyltransferase-deficient mice"Carcinogenesis. 21. 301-305 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Miyako, M.Sekiguchi et al.: "Accumulation of adenine DNA glycosylase-sensitive sites in human mitochondrial DNA"J.Biol.Chem.. 275. 123526-12330 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H.Shimokawa, M.Sekiguchi et al.: "Functional significance of conserved residue in the phophohydrolase module of Escherichia coli MutT potein"Nucl.Acids Res.. 28. 3240-4249 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] A.Shiraishi, M.Sekiguchi et al.: "Increased susceptibility to chemotherapeutic alkylating agents of mice deficient in DNA repair methyltransferase"Carcinogenesis. 21. 1879-1883 (2000)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2002-03-26  

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