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Development of an efficient screening system to identify novel bone metabolism-related genes using the exchangeable gene trap mutagenesis mouse models.

Research Project

Project/Area Number 26462305
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Orthopaedic surgery
Research InstitutionUniversity of Miyazaki

Principal Investigator

Kurogi Syuji  宮崎大学, 医学部, 医員 (40418843)

Co-Investigator(Kenkyū-buntansha) 帖佐 悦男  宮崎大学, 医学部, 教授 (00236837)
関本 朝久  宮崎大学, 医学部, 講師 (60305000)
荒木 正健  熊本大学, 生命資源研究・支援センター, 准教授 (80271609)
荒木 喜美  熊本大学, 生命資源研究・支援センター, 教授 (90211705)
Research Collaborator Funamoto Taro  
Ohta Tomomi  
Nakamura Shihoko  
Project Period (FY) 2014-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords骨代謝 / 可変型遺伝子トラップ法 / 骨粗鬆症 / ロコモティブシンドローム / 骨粗しょう症 / 骨代謝スクリーニング
Outline of Final Research Achievements

We have developed an efficient screening system to identify novel genes involved in bone metabolism using mutant mouse strains registered in the Exchangeable Gene Trap Clones (EGTC) database. From 1278 trap clones in the EGTC, 52 candidate lines were selected in the first screening, which were decided referring to 4 criteria. Bone morphometric analysis (BMA), biomechanical strength analysis (BSA), etc. were then performed on the candidate lines as the second screening, and 41 lines (78.8%) showed abnormalities in either BMA or BSA. In the first screening “X-gal” was significantly efficient (P = 0.0099). Thus, our screening system using the EGTC mouse lines is extremely efficient in identifying novel genes involved in bone metabolism. The gene trap lines identified as abnormal using this screening approach are highly likely to trap important genes for bone metabolism, therefore these selected trap mice would be valuable for bone research by acting as novel bio-resources.

Report

(5 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (8 results)

All 2017 2016 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (7 results) (of which Int'l Joint Research: 1 results)

  • [Journal Article] Development of an efficient screening system to identify novel bone metabolism-related genes using the exchangeable gene trap mutagenesis mouse models2017

    • Author(s)
      Syuji Kurogi, Tomohisa Sekimoto, Taro Funamoto, Tomomi Ohta, Shihoko Nakamura, Takuya Nagai, Mai Nakahara, Kumiko Yoshinobu, Kimi Araki, Masatake Araki, Etsuo Chosa
    • Journal Title

      Scientific Reports

      Volume: 7 Issue: 1 Pages: 40692-40692

    • DOI

      10.1038/srep40692

    • Related Report
      2017 Annual Research Report 2016 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Presentation] 可変型遺伝子トラップ法を用いた骨軟骨に異常をきたす新規遺伝子群の探索および機能解析2016

    • Author(s)
      黒木修司
    • Organizer
      日本整形外科学会基礎学術集会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2016-10-13
    • Related Report
      2016 Research-status Report
  • [Presentation] Construction of a novel gene library related to osteogenic disorder using exchangeable gene trap mutagenesis2015

    • Author(s)
      Shihoko Nakamura, Tomohisa Sekimoto, Shuji Kurogi
    • Organizer
      Australian New Zealand Bone & Mineral Society Annual Scientific Meeting 2015
    • Place of Presentation
      Hotel Grand Chancellor Hobart, タスマニア(オーストラリア)
    • Year and Date
      2015-11-01
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] 可変型遺伝子トラップ法を用いた骨軟骨異常を来す新規遺伝子群のライブラリー構築2015

    • Author(s)
      永井琢哉、関本朝久、黒木修司
    • Organizer
      第30回日本整形外科学会基礎学術集会
    • Place of Presentation
      富山市民プラザ(富山県富山市)
    • Year and Date
      2015-10-22
    • Related Report
      2015 Research-status Report
  • [Presentation] 可変型遺伝子トラップ法を用いた骨軟骨に異常をきたす新規遺伝子群の探索および機能解析2015

    • Author(s)
      舩元太郎、関本朝久、黒木修司
    • Organizer
      産学・地域連携センター 第22回技術・研究発表交流会
    • Place of Presentation
      宮崎市民プラザ(宮崎県宮崎市)
    • Year and Date
      2015-09-30
    • Related Report
      2015 Research-status Report
  • [Presentation] 可変型遺伝子トラップ法を用いた骨代謝異常をきたす新規遺伝子群のライブラリー構築2015

    • Author(s)
      中村志保子、関本朝久、黒木修司
    • Organizer
      第33回日本骨代謝学会学術集会
    • Place of Presentation
      京王プラザホテル(東京都新宿区)
    • Year and Date
      2015-07-23
    • Related Report
      2015 Research-status Report
  • [Presentation] 可変型遺伝子トラップ法で作製したTmem161a欠損マウスは明らかな骨量増加を呈する2014

    • Author(s)
      黒木修司
    • Organizer
      第29回日本整形外科学会基礎学術集会
    • Place of Presentation
      城山観光ホテル
    • Year and Date
      2014-10-09 – 2014-10-10
    • Related Report
      2014 Research-status Report
  • [Presentation] 可変型遺伝子トラップ法を用いた骨代謝に関与する新規遺伝子群の効率的スクリーニング2014

    • Author(s)
      黒木修司
    • Organizer
      第32回日本骨代謝学会学術集会
    • Place of Presentation
      大阪国際会議場
    • Year and Date
      2014-07-24 – 2014-07-26
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2019-03-29  

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