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Model experimental systems for plant redox regulation and analysis of the stress-tolerance mechanism

Research Project

Project/Area Number 18580339
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Applied molecular and cellular biology
Research InstitutionShimane University

Principal Investigator

ISHIKAWA Takahiro  Shimane University, Faculty of Life and Environmental Sciences, Associate Professor (60285385)

Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥240,000)
Fiscal Year 2007: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2006: ¥2,600,000 (Direct Cost: ¥2,600,000)
Keywordsredox / plant culture cell / ascorbate peroxidase / environmental stress / stress-responsible genes
Research Abstract

To establish a model experimental system for plant redox regulation of gene expression, we made transgenic tobacco BY-2 cells and Arabidopsis plants harboring overexpession and silencing system for ascorbate peroxidase (APX), a key enzyme of H_2O_2-scavenging in plants, inducing by estrogen supplementation. We hired pMDC7 and developed pXR as the vector for the aim. The resultant tobacco BY-2 line transformed with antisense construct for cytosolic APX, named AtAS3, showed 40 % less APX activity compared with untransformed BY-2 cells after addition of 25 μW estrogen. The cellular H_2O_2 level in AtAS3 was significantly increased by the silencing of cytosolic APX. Interestingly, AtAS3 showed increasing tolerance against salt and heat share after estrogen induction. These results indicated that this line is useful fir the model system of redox gene regulation. By the screening of suppressive subtraction hybridization (SSH) method, I have collected several possibilities for redox-responsible genes, including the known genes like HSPs.
Furthermore, transgenic Arabidopsis plants silencing chloroplastic APX expression with RNAi by pXR introduction showed lower chloroplastic APX gene expression and its enzyme activity. The effect of the silencing on the APX expression was stable and lasting at least for six days after estrogen treatment. Microsaray analysis showed that approximately 400 and 250 genes were upregulated and downregulated, respectively. Among them, the genes related to signal transduction and metabolism were occupied, indicating there are many possibilities including chloroplast-to-nucleus signal transduction. Beside the APX-suppression systems describing above, we have also developed APX-overexpressors in tobacco BY-2 and Arabidopsis plants.
Overall, we have proved that APX plays a central rule on cellular redox regulation, and have successfully developed the model experimental system fir elucidating redox gene regulation mechanism in plants.

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (4 results)

All 2007 2006

All Presentation (4 results)

  • [Presentation] 酸化的シグナリングを介した環境ストレス応答2007

    • Author(s)
      丸田 隆典
    • Organizer
      日本分子生物学会
    • Place of Presentation
      横浜市
    • Year and Date
      2007-12-13
    • Related Report
      2007 Annual Research Report
  • [Presentation] Environmental stress response mediated by oxidative signaling2007

    • Author(s)
      Maruta, T., Yabuta, Y., Ishikawa, T., Shigeoka, S
    • Organizer
      30th The Molecular Biology Society of Japan
    • Place of Presentation
      Yokohama, Japan
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] レドックス状態改変植物細胞の作製と環境ストレス応答性の検討.2006

    • Author(s)
      石川孝博
    • Organizer
      日本生化学会中国・四国支部例会
    • Place of Presentation
      島根県松江市
    • Year and Date
      2006-05-12
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Generation of model plant cells with altered cellular redox status and it's response to environmental stresses2006

    • Author(s)
      Morimoto, Y., Sawa, Y., Shibata, H., Ishiakwa, T
    • Organizer
      47th Japanese Society of Biochemistry, chugoku-shikoku branch
    • Place of Presentation
      Matsue, Japan
    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2007 Final Research Report Summary

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Published: 2006-04-01   Modified: 2016-04-21  

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