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Generic cell ablation system: sterile-insect technique for control of infectious disease vector and prevention of leakage of beneficial insect strains

Research Project

Project/Area Number 17K08161
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Insect science
Research InstitutionNational Agriculture and Food Research Organization

Principal Investigator

Kasashima Megumi  国立研究開発法人農業・食品産業技術総合研究機構, 生物機能利用研究部門, 上級研究員 (90458290)

Co-Investigator(Kenkyū-buntansha) 山本 大介  自治医科大学, 医学部, 准教授 (90597189)
Project Period (FY) 2017-04-01 – 2023-03-31
Project Status Completed (Fiscal Year 2022)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
KeywordsTransgenic silkworm / Genome editing / Specific gene expression / Sterilization / apoptosis / cell death / CRISPR-Cas9 / ゲノム編集 / ノックイン系統 / カイコ / 組織特異的プロモーター / 遺伝子ノックイン / 組織特異的発現 / 不妊化 / SIT / 遺伝学 / 昆虫制御 / 有用昆虫 / 病気媒介昆虫
Outline of Final Research Achievements

Considering the Genetic Resource Security Strategy, it is necessary to develop a practical technique for sterilizing silkworms in order to prevent the unauthorized export or dissemination of valuable strains. First, we developed an effector utilizing mammalian apoptosis-associated gene and verified its ability to induce cell death in silkworms. Next, we expressed this gene in the testes of malaria-vector mosquitoes and confirmed that sterilization of male mosquito can be achieved. In addition, to develop the site-specific knock-in technology required for inducible sterilization, we established a knock-in strain by inserting the Gal4 gene that is expressed under the native initiation codon of the silk gland expressed gene.

Academic Significance and Societal Importance of the Research Achievements

The apoptosis gene used in this study can induce cell death in vivo regardless of insect type or tissue. It can be used not only as a sterilization technique, but also as a highly versatile system for functional analysis of nerves or specific tissues in Entomology.

Report

(7 results)
  • 2022 Annual Research Report   Final Research Report ( PDF )
  • 2021 Research-status Report
  • 2020 Research-status Report
  • 2019 Research-status Report
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (5 results)

All 2019

All Journal Article (1 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (4 results)

  • [Journal Article] A synthetic male-specific sterilization system using the mammalian pro-apoptotic factor in a malaria vector mosquito2019

    • Author(s)
      Daisuke S. Yamamoto, Megumi Sumitani, Katsumi Kasashima, Hideki Sezutsu, Hiroyuki Matsuoka & Hirotomo Kato
    • Journal Title

      Scientific Reports

      Volume: 印刷中

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] カイコ創薬の新展開 ~蚕業革命の推進~ TFAM の過剰発現によるミトコンドリア機能異常カイコモデルの構築2019

    • Author(s)
      笠嶋めぐみ・笠嶋克巳・近藤まり・一ノ瀬清・行弘文子・田中博光・飯塚 哲也・内野恵郎、瀬筒秀樹
    • Organizer
      日本薬学会第139会年会
    • Related Report
      2018 Research-status Report
  • [Presentation] TFAMの過剰発現による疾患モデルカイコの構築2019

    • Author(s)
      一ノ瀬清・近藤まり・山田信人・飯塚哲也・瀬筒秀樹・笠嶋めぐみ
    • Organizer
      つくば医工連携フォーラム2019
    • Related Report
      2018 Research-status Report
  • [Presentation] doublesexノックアウトハマダラカの中朝における遺伝子転写産物の解析2019

    • Author(s)
      山本大介・笠嶋めぐみ・加藤大智
    • Organizer
      日本応用動物学会
    • Related Report
      2018 Research-status Report
  • [Presentation] BmTFAM 過剰発現カイコの表現型解析2019

    • Author(s)
      一ノ瀬清・近藤まり・山田信人・飯塚哲也・瀬筒秀樹・ 笠嶋めぐみ
    • Organizer
      平成31年度蚕糸・昆虫機能利用学術講演会
    • Related Report
      2018 Research-status Report

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Published: 2017-04-28   Modified: 2024-01-30  

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