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Determination of functional sequences available for horticulture in viroid nucleotide

Research Project

Project/Area Number 20380020
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Horticulture/Landscape architecture
Research InstitutionKyoto University

Principal Investigator

HOSOKAWA Munetaka  Kyoto University, 農学研究科, 准教授 (40301246)

Co-Investigator(Kenkyū-buntansha) KAIDO Masanori  京都大学, 農学研究科, 助教 (20314247)
MATSUSHITA Yousuke  花き研究所, 研究員 (00414665)
Project Period (FY) 2008 – 2010
Project Status Completed (Fiscal Year 2010)
Budget Amount *help
¥19,500,000 (Direct Cost: ¥15,000,000、Indirect Cost: ¥4,500,000)
Fiscal Year 2010: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2009: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Fiscal Year 2008: ¥14,820,000 (Direct Cost: ¥11,400,000、Indirect Cost: ¥3,420,000)
Keywordsウイロイド / キク / 機能性RNA / プロモーター / 長距離移行性 / キクわい化ウイロイド(CSVd) / ポスピウイロイド / 長距離移行 / タバコ / アラビドプシス / プロモーター活性 / キクわい化ウイロイド / 開花反応 / 局在性 / CSVd / CChMVd / 核
Research Abstract

The full length of CSVd or its partial sequence was connected in additional sequences, the long-distance transmissibility of additional sequences were examined. Since the additional sequences which were added with the sequence of a partial CSVd had a long-distance transferability, it was presumed that there is a capability in the sequence of CSVd for transferring the RNA for a long distance.
In order to confirm this fact, a tobacco recombinant which excessively develops similar sequences was created regarding the partial sequence series of CSVd. Although a section of Nicotiana benthamiana was grafted in the tobacco recombinant (Nicotiana tabacum) with CSVd of full-length sequences and the long-distance transferability of addition sequences was examined, a long-distance transferability was not found. The examinations of other sequences are still ongoing.
Moreover, it was indicated that CSVd sequences have a function for reinforcing 35S promoter's activity. Furthermore, since the ability for transcribing RNA using the template of mRNA which CSVd is expected to have was confirmed in the recombinant tobacco, it is thought that the mRNA multiplication in a plant is possible.

Report

(4 results)
  • 2010 Annual Research Report   Final Research Report ( PDF )
  • 2009 Annual Research Report
  • 2008 Annual Research Report
  • Research Products

    (4 results)

All 2011 2009

All Journal Article (3 results) (of which Peer Reviewed: 1 results) Presentation (1 results)

  • [Journal Article] 新しいウイロイドフリーの方法としての超微小茎頂分裂組織培養法(仮題)2011

    • Author(s)
      細川宗孝
    • Journal Title

      植物防疫 (掲載確定)

    • Related Report
      2010 Final Research Report
  • [Journal Article] ウイロイドフリー植物作出のための新手法・超微小茎頂分裂組織培養法2011

    • Author(s)
      細川宗孝
    • Journal Title

      植物防疫

      Volume: (未定 掲載確定)

    • NAID

      40018930667

    • Related Report
      2010 Annual Research Report
  • [Journal Article] In vitro-transcribed Chrysanthemum stunt viroid RNA is infectious to chrysanthemum and other plants2009

    • Author(s)
      Matsushita Y, P. K. R. Kumar
    • Journal Title

      Phytopathology 99

      Pages: 58-66

    • Related Report
      2008 Annual Research Report
    • Peer Reviewed
  • [Presentation] キクわい化ウイロイドに抵抗性を持つキク品種の探索2011

    • Author(s)
      細川宗孝・鍋島朋之・矢野志野布・大石一史・土井元章
    • Organizer
      園芸学会
    • Place of Presentation
      宇都宮大学
    • Year and Date
      2011-03-20
    • Related Report
      2010 Annual Research Report

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Published: 2008-04-01   Modified: 2016-04-21  

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