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Analysis of the roles of the cell polarity protein Morg1 in embryonic development

Research Project

Project/Area Number 16K21221
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field General medical chemistry
Pathological medical chemistry
Research InstitutionKyushu University

Principal Investigator

Hayase Junya  九州大学, 医学研究院, 特別研究員 (PD) (40621686)

Project Period (FY) 2016-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2017: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2016: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
KeywordsMorg1 / apico-basal polarity / 細胞極性
Outline of Final Research Achievements

Epithelial cells and endothelial cells in multicellular organisms that form lumens of organs or vascular lumens, respectively, have distinct apical and basolateral membrane domains, which play crucial roles in maintaining the body through absorbing nutrients and excreting wastes. The membrane domain asymmetry, which is called apico-basal polarity, is dependent on the polarity complex Par6-aPKC complex and the Rho family small GTPase. Recently, we identified the novel polarity protein Morg1, which was found to be essential for embryonic development in mice. The present study clarified that Morg1 plays essential roles in vasculogenesis during embryonic development and physically interacts with GEF-H1, a RhoA-specific guanine-nucleotide exchange factor.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • Research Products

    (3 results)

All 2018 2017

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 2 results,  Acknowledgement Compliant: 2 results)

  • [Journal Article] Differential cell surface recruitment of the superoxide-producing NADPH oxidases Nox1, Nox2 and Nox5: The role of the small GTPase Sar12018

    • Author(s)
      Kiyohara Takuya、Miyano Kei、Kamakura Sachiko、Hayase Junya、Chishiki Kanako、Kohda Akira、Sumimoto Hideki
    • Journal Title

      Genes to Cells

      Volume: 印刷中 Issue: 6 Pages: 480-493

    • DOI

      10.1111/gtc.12590

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Ric-8A-mediated stabilization of the trimeric G protein subunit Gαi is inhibited by pertussis toxin-catalyzed ADP-ribosylation2017

    • Author(s)
      Kanako Chishiki, Sachiko Kamakura, Junya Hayase, Satoru Yuzawa, Hideki Sumimoto
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: 483 Issue: 3 Pages: 941-945

    • DOI

      10.1016/j.bbrc.2017.01.036

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] Ric-8A, an activator protein Gαi, controls mammalian epithelial cell polarity for tight junction assembly and cystogenesis2017

    • Author(s)
      Kanako Chishiki, Sachiko Kamakura, Junya Hayase, Hideki Sumimoto
    • Journal Title

      Genes to Cells

      Volume: 22 Issue: 3 Pages: 293-309

    • DOI

      10.1111/gtc.12477

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant

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Published: 2016-04-21   Modified: 2019-03-29  

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