• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Identification of molecular mechanism for the establishment of circadian clock during development.

Research Project

Project/Area Number 26670111
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Environmental physiology(including physical medicine and nutritional physiology)
Research InstitutionTokyo Medical and Dental University

Principal Investigator

Hirayama Jun  東京医科歯科大学, 難治疾患研究所, 准教授 (90510363)

Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords概日リズム / ゼブラフィッシュ / 転写
Outline of Final Research Achievements

Circadian clocks constitute ubiquitous processes that regulate various biochemical and physiological events occurring with a 24 hour periodicity. Zebrafish eggs are fertilized externally and embryos develop rapidly from fertilized eggs to larvae that swim, making them an excellent model for studies of vertebrate circadian clocks’ establish. Previous studies have reported that circadian rhythms in clock-controlled genes’ expression and locomotor activity in zebrafish larvae are not observed when zebrafish are raised in constant conditions. These rhythms emerge only if embryos are exposed to environmental signals such as light. However the molecular mechanisms underlying how these circadian rhythms are set in motion during development remains unclear. This study used chemical library and have identified the signaling pathways and transcription factors, which are involved in establishment of circadian clock during development.

Report

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

    (6 results)

All 2015 2014 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (4 results) (of which Int'l Joint Research: 2 results,  Invited: 2 results) Remarks (1 results)

  • [Journal Article] The PDZ-binding motif of Yes-associated protein is required for its co-activation of TEAD-mediated CTGF transcription and oncogenic cell transforming activity.2014

    • Author(s)
      Shimomura T, Miyamura N, H ata S, Miura R, Hirayama J, N ishina H
    • Journal Title

      Biochemical and Biophysical Research Communi cations

      Volume: 443 Issue: 3 Pages: 917-923

    • DOI

      10.1016/j.bbrc.2013.12.100

    • Related Report
      2014 Research-status Report
    • Peer Reviewed
  • [Presentation] Molecular mechanism for the light-dependent establishment of circadian clock during zebrafish development.2015

    • Author(s)
      Hirayama Jun
    • Organizer
      Seminar in National Health Research Institutes
    • Place of Presentation
      Zhunan, Taiwan
    • Year and Date
      2015-11-19
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] Molecular mechanism for the light-dependent establishment of circadian clock during development in zebrafish2015

    • Author(s)
      Hirayama Jun, Nishina Hiroshi
    • Organizer
      7th Asia and Oceania Conference for Photobiology
    • Place of Presentation
      Taipei, Taiwan
    • Year and Date
      2015-11-15
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] ゼブラフィッシュ概日リズムの光同調を担うシグナル経路の解析2014

    • Author(s)
      平山順、川原敦雄、仁科博史
    • Organizer
      第21回日本時間生物学会学術大会
    • Place of Presentation
      福岡 九州大学医学部 百年講堂
    • Year and Date
      2014-11-07 – 2014-11-09
    • Related Report
      2014 Research-status Report
  • [Presentation] Study on a light signaling pathway for circadian entrainment in zebrafish2014

    • Author(s)
      平山順、川原敦雄、仁科博史
    • Organizer
      20th Japanese Medaka and Zebrafish Meeting
    • Place of Presentation
      東京 慶應義塾大学薬学部 芝共立キャンパス
    • Year and Date
      2014-09-20 – 2014-09-21
    • Related Report
      2014 Research-status Report
  • [Remarks] 東京医科歯科大学難治疾患研究所 発生再生生物学分野

    • URL

      http://www.tmd.ac.jp/mri/dbio/

    • Related Report
      2015 Annual Research Report 2014 Research-status Report

URL: 

Published: 2014-04-04   Modified: 2017-05-10  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi