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Evolution of fast skeletal myosin heavy chain genes of fish

Research Project

Project/Area Number 23780214
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Fisheries chemistry
Research InstitutionKitasato University

Principal Investigator

IKEDA Daisuke  北里大学, 海洋生命科学部, 講師 (00466806)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2011: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywordsミオシン重鎖 / ゲノム / 分子進化 / 発生進化 / ヤツメウナギ
Research Abstract

In the present study, to elucidate the evolutionary relationship of fast skeletal myosin heavy chain genes (MYHs), MYHs of teleosts and tetrapods were compared with those of agnathan lampreys, one of the most primitive jawless fish. As a result, lampreys contained at least three fast skeletal MYHs which were clustered in ahead-to-tail manner on a single genomic region. Moreover, there was an apparent synteny in the corresponding MYH cluster regions between lamprey and tetrapod, implying that fast skeletal MYH clustering was a very early event in vertebrate evolution. Although zebrafish MYH promoters showed apparent activity to direct reporter gene expression in myogenic cells derived from mouse, those of lamprey had no activity. These results suggest thatthe common ancestor of vertebrate fast skeletal MYHs had been diverged into those of agnathan fish, teleosts and tetrapods. Tetrapods are assumed to have subsequently developed a transcriptional network system different from that of agnathan fish.

Report

(3 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Research-status Report
  • Research Products

    (8 results)

All 2013 2012 2011 Other

All Presentation (8 results)

  • [Presentation] 培養細胞発現系を用いたヤツメウナギおよびゼブラフィッシュ・ミオシン重鎖遺伝子プロモーター 領域の機能比較2013

    • Author(s)
      池田大介、平野茂樹、菅野信弘、渡部終五
    • Organizer
      平成25年度日本水産学会春季大会
    • Place of Presentation
      東京海洋大学品川キャンパス(東京都)
    • Year and Date
      2013-03-28
    • Related Report
      2012 Final Research Report
  • [Presentation] 培養細胞を用いたカワヤツメ速筋型ミオシン 重鎖遺伝子プロモーター領域の解析2012

    • Author(s)
      池田大介、平野茂樹、菅野信弘、渡部終五
    • Organizer
      平成24年度日本水産学会秋季大会
    • Place of Presentation
      水産大学校 (山口県)
    • Year and Date
      2012-09-15
    • Related Report
      2012 Final Research Report
  • [Presentation] カワヤツメ速筋型ミオシン重鎖遺伝子クラスターの塩基配列決定とプロモーター領域の解析2012

    • Author(s)
      池田大介、平野茂樹、菅野信弘、渡部終五
    • Organizer
      平成24年度日本水産学会春季大会
    • Place of Presentation
      東京海洋大学品川キャンパス(東京都)
    • Year and Date
      2012-03-27
    • Related Report
      2012 Final Research Report
  • [Presentation] Myosin heavy chain clusters in fish2011

    • Author(s)
      Daisuke Ikeda
    • Organizer
      The International Symposium on Muscle Biochemistry
    • Place of Presentation
      東京大学本郷キャンパス(東京都)
    • Year and Date
      2011-10-28
    • Related Report
      2012 Final Research Report
  • [Presentation] 培養細胞発現系を用いたヤツメウナギおよびゼブラフィッシュ・ミオシン重鎖遺伝子プロモーター 領域の機能比較

    • Author(s)
      池田大介ら
    • Organizer
      平成25年度日本水産学会春季大会
    • Place of Presentation
      東京海洋大学品川キャンパス
    • Related Report
      2012 Annual Research Report
  • [Presentation] 培養細胞を用いたカワヤツメ速筋型ミオシン 重鎖遺伝子プロモーター領域の解析

    • Author(s)
      池田大介ら
    • Organizer
      平成24年度日本水産学会秋季大会
    • Place of Presentation
      水産大学校
    • Related Report
      2012 Annual Research Report
  • [Presentation] カワヤツメ速筋型ミオシン重鎖遺伝子クラスターの塩基配列決定とプロモーター領域の解析

    • Author(s)
      池田大介、平野茂樹、菅野信弘、渡部終五
    • Organizer
      平成23年度日本水産学会春季大会
    • Place of Presentation
      東京海洋大学 (港区)
    • Related Report
      2011 Research-status Report
  • [Presentation] Myosin heavy chain clusters in fish

    • Author(s)
      Daisuke Ikeda
    • Organizer
      The International Symposium on Muscle Biochemistry(招待講演)
    • Place of Presentation
      東京大学 (文京区)
    • Related Report
      2011 Research-status Report

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Published: 2011-08-05   Modified: 2019-07-29  

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