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2000 Fiscal Year Final Research Report Summary

Molecular basis of circadian rhythms : function of clock genes

Research Project

Project/Area Number 11694199
Research Category

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

Allocation TypeSingle-year Grants
Section一般
Research Field Cell biology
Research InstitutionNagoya University

Principal Investigator

KONDO Takao  Nagoya University, Graduate School of Science, professor, 大学院・理学研究科, 教授 (10124223)

Co-Investigator(Kenkyū-buntansha) SHIBATA Shigenobu  Waseda University, School of Human Sciences, Professor, 人間科学部, 教授 (10162629)
EBIHARA Shizufumi  Nagoya University, Graduate School of Bioagricultural Science, Professor, 生命農学研究科, 教授 (50135331)
HONMA Kenichi  Hokkaido University, Graduate School of Medicine, Professor, 大学院・医学研究科, 教授 (40113625)
OKAMURA Hitoshi  Kobe University, School of Medicine, Professor, 医学部, 教授 (60158813)
FUKADA Yoshitaka  Tokyo University, Graduate School of Science, Professor, 大学院・理学研究科, 教授 (80165258)
Project Period (FY) 1999 – 2000
Keywordscyanobacteria / mouse / circadian clock / clock genes / Drosophila / protein interaction / suprachiasmatic nuclei / phosphorylation
Research Abstract

Circadian clock functions in almost all organisms and function to adapt the life to daily alternating environment. Molecular mechanism of the circadian clock is one of the most interesting subject of basic biology nowadays. Recent advances in molecular genetic approaches to the clock genes identified several clock genes in model organisms. Recently, clock genes of cyanobacteria and mammals was cloned by Japanese scientists and US-Japan collaboration become more important for advance in this field. The project had been applied as International research grants and accepted as basic research grants for 1999-2000. The Center of the biological timing (NSF) is the partner group of US scientists. To promote collaboration and individual research projects of the project members, the first symposium had been held at Hawaii, in 1999 and the second at Kyoto in 2000. In both symposiums, many non-member scientists were also invited and there were very active presentation and discussion, which then trigger collaboration and simulate research of project members. In addition to two symposiums, domestic workshop was held at Inuyama, Aichi, in late 1999 to promote and activate young Japanese scientist who, otherwise, would not have a chance to discuss because many of them belong to different communities.
With these activities, new collaboration between Japan and US was started and some collaborations which already started were promoted. Also, the information of the symposium were very stimulus for each project members. After all, with this project, understanding for molecular basis of the circadian clock has been greatly advanced and we recognized that simple negative feedback dogma is insufficient to explain circadian characteristics that features the circadian oscillate to be adaptive. To obtain full understanding the clock at molecular level, many unknown processes and whole cellular metabolism should be included in the circadian system.

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Nishiwaki T: "Nucleotide binding and autophosphorylation of the clock protein KaiC as a circadian timing process of cyanobacteria."Proc.Natl.Acad.Sci.. 97. 495-499 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Hirota S: "Spectroscopic and electrochemical studies on structural change of plastcyanin and its tyrosine 83 mutants induced by interaction with lysine peptide."Biochemistry. 39. 6357-6364 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Schmitz,O: "CikA, a bacteriophytochrome that resets the cyanobacterial circadian clock."Science. 289. 765-768 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamaguchi S: "Real time monitoring of clock gene expression in the living mouse."Nature. 409. 684 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yuko Harada: "Circadian activation of bullfrog retinal mitogen-activated protein kinase associates with oscillator function."J.Biol.Chem.. 275. 37078-37085 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Asai M: "Administration of melatonin in drinking water promotes the phase advance of light-dark cycle in senescence-accelerated mice, SAMR1 but not SAMP8."Brain Research. 876. 220-224 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nishiwaki T, Iwasaki, H., Ishiura, M.and T.Kondo: "Nucleotide binding and autophosphorylation of the clock protein KaiC as a circadian timing process of cyanobacteria."Proc.Natl.Acad.Sci.. 97. 495-499 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hirota, S., et al: "Spectroscopic and electrochemical studies on structural change of plastcyanin and its tyrosine 83 mutants induced by interaction with lysine peptide."Biochemistry. 39. 6357-6364 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Schimitz, O, M Katayama, S.B.Williams, T.Kondo, S.S.Golden: "CikA, a bacteriophytochrome that resets the cyanobacterial circadian clock."Science. 289. 765-768 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yamaguchi S, Kobayashi M, Mitsui S, Ishida Y, van der Horst GTJ, Suzuki M, Shibata S, Okamura H: "Real time monitoring of clock gene expression in the living mouse."Nature. 409. 684 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yuko Harada, Kamon Sanada and Yoshitaka Fukada: "Circadian activation of bullfrog retinal mitogen-activated protein kinase associates with oscillator function."J.Biol.Chem.. 275. 37078-37085 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Asai, M., et al: "Administration of melatonin in drinking water promotes the phase advance of light-dark cycle in senescence-accelerated mice, SAMR1 but not SAMP8."Brain Research. 876. 220-224 (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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