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Molecular functions of the Ssk1 osmo-regulator in the yeast HOG MAPK pathway

Research Project

Project/Area Number 17570105
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Functional biochemistry
Research InstitutionThe University of Tokyo

Principal Investigator

TATEBAYASHI Kazuo  The University of Tokyo, Institute of Medical Science, Research Associate, 医科学研究所, 助手 (50272498)

Project Period (FY) 2005 – 2006
Project Status Completed (Fiscal Year 2006)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2005: ¥1,800,000 (Direct Cost: ¥1,800,000)
Keywordsyeast / stress response / high osmolarity / MAP kinase cascade / HOG pathway / signal transduction / 酵母 / MAPキナーゼ / リン酸化 / Ssk1 / Ssk2 / Ssk22
Research Abstract

Yeast Ste11 MAPKKK takes part in three different MAPK signaling modules that respond to, respectively, mating pheromones, osmostress, and nutritional conditions. Nevertheless, each MAPK pathway is activated only by the cognate stimulus. To investigate how osmostress activates only the Hog1 MAP kinase module (HOG pathway), we isolated and characterized constitutively activated alleles in three key genes involved in the pathway, namely STE11, STE50, and SHO1. We found that Cdc42 not only activates the upstream kinases in the HOG pathway, Ste20 and Cla4, but also binds to Ste11-bound Ste50, thereby bringing activated Ste20/Cla4 and their substrate Ste11 together. Subsequently, activated Ste11 and its HOG pathway-specific substrate, Pbs2 MAPKK, are brought together by binding of the Ste50-Ste11 complex to the cytoplasmic domain of Sho1, to which Pbs2 is also bound. Thus, both Sho1 and Ste50 act as adaptive docking proteins that restrict the flow of the osmostress signal from Ste20/Cla4 to Pbs2, via Ste11.

Report

(3 results)
  • 2006 Annual Research Report   Final Research Report Summary
  • 2005 Annual Research Report
  • Research Products

    (6 results)

All 2006 2005

All Journal Article (6 results)

  • [Journal Article] Adaptor functions of Cdc42, Ste50, and Sho1 in the yeast osmoregulatory HOG MAPK pathway2006

    • Author(s)
      Tatebayashi K
    • Journal Title

      The EMBO Journal 25

      Pages: 3033-3044

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Adaptor functions of Cdc42, Ste50, and Sho1 in the yeast osmoregulatory HOG MAPK pathway.2006

    • Author(s)
      Tatebayashi K, Yamamoto K, Tanaka K, Tomida T, Maruoka T, Kasukawa E, Saito H
    • Journal Title

      EMBO J. 25

      Pages: 3033-3044

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Adaptor functions of Cdc42, Ste50, and Shol in the yeast osmoregulatory HOG MARK pathway2006

    • Author(s)
      Tatebayashi K
    • Journal Title

      The EMBO Journal 25

      Pages: 3033-3044

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Conserved docking site is essential for activation of mammalian MAP kinase kinases by specific MAP kinase kinase kinases2005

    • Author(s)
      Takekawa M
    • Journal Title

      Mol.Cell 18

      Pages: 295-306

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Conserved docking site is essential for activation of mammalian MAP kinase kinases by specific MAP kinase kinase kinases.2005

    • Author(s)
      Takekawa M, Tatebayashi K, Saito H.
    • Journal Title

      Mol.Cell 18

      Pages: 295-306

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Conserved docking site is essential for activation of mammalian MAP kinase kinases by specific MAP kinase kinase kinases2005

    • Author(s)
      Takekawa M
    • Journal Title

      Molecular Cell 18

      Pages: 295-306

    • Related Report
      2005 Annual Research Report

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Published: 2005-04-01   Modified: 2016-04-21  

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