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Identification of signaling pathways regulating multiciliate cell differentiation, maturation and function in early embryos

Research Project

Project/Area Number 26440123
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Developmental biology
Research InstitutionKyoto University

Principal Investigator

KUSAKABE Morioh  京都大学, 生命科学研究科, 講師 (80378843)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywordsアフリカツメガエル / シグナル伝達 / 多繊毛
Outline of Final Research Achievements

Multiciliate cells, which are found in epithelia of various organs in vertebrates, generate extracellular fluid flow along epithelial surfaces by several hundreds of motile cilia. In this study, we show that mab21-l3, which has been identified as a Ras-repressed gene in our previous study, is required for early specification of multiciliate cells and ion-transporting ionocytes. Moreover, we find that an atypical MAPK member, ERK7, regulates ciliogenesis by phosphorylating the actin regulator CapZIP.

Report

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

    (5 results)

All 2015 2014

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Acknowledgement Compliant: 2 results) Presentation (3 results) (of which Invited: 1 results)

  • [Journal Article] ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled2015

    • Author(s)
      Miyatake K. et al.
    • Journal Title

      Nature Commun.

      Volume: 6 Issue: 1 Pages: 1-12

    • DOI

      10.1038/ncomms7666

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] mab21-l3 regulates cell fate specification of multiciliate cells and ionocytes2015

    • Author(s)
      Chika Takahashi, Morioh Kusakabe, Toshiyasu Suzuki, Koichi Miyatake and Eisuke Nishida
    • Journal Title

      Nature Communications

      Volume: 6 (6017) Issue: 1 Pages: 1-13

    • DOI

      10.1038/ncomms7017

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] A Notch-repressed gene mab21-l3 is a key regulator for cell fate specification of multiciliate cells and ionocytes.2015

    • Author(s)
      Morioh Kusakabe, Chika Takahashi, Eisuke Nishida
    • Organizer
      BMB2015(第38回日本分子生物学会年会、第88回日本生化学会大会 合同大会)
    • Place of Presentation
      神戸ポートアイランド、神戸、日本
    • Year and Date
      2015-12-01
    • Related Report
      2015 Research-status Report
    • Invited
  • [Presentation] ERK7, a novel regulator of ciliogenesis, is required for basal body migration.2014

    • Author(s)
      Miyatake K, Kusakabe M, Takahashi C, Nishida E.
    • Organizer
      15th International Xenopus Conference
    • Place of Presentation
      Pacific Grove, California, USA
    • Year and Date
      2014-08-24 – 2014-08-28
    • Related Report
      2014 Research-status Report
  • [Presentation] Xenopus mab21-l3 is required for cell fate specification of multiciliate cells and ionocytes.2014

    • Author(s)
      Takahashi C, Kusakabe M, Suzuki T, Miyatake K, Nishida E.
    • Organizer
      15th International Xenopus Conference
    • Place of Presentation
      Pacific Grove, California, USA
    • Year and Date
      2014-08-24 – 2014-08-28
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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