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Development of translational regulation platform of circadian rhythms using a novel poly(A) determination method

Research Project

Project/Area Number 25640100
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Genome biology
Research InstitutionKanazawa University

Principal Investigator

TEI Hajime  金沢大学, 理工研究域自然システム学系, 教授 (00242115)

Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2013: ¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Keywords概日リズム / 時計遺伝子 / 視交叉上核 / 翻訳制御 / Period1 / poly(A) / Peirod1 / Poly(A) / Lark
Outline of Final Research Achievements

In general, the length of poly (A) in eukaryotic mRNA shows a wide distribution, and at present, there is no precise and simple method to determine it. A novel method for its determination was developed with the improvement of conventional anchored RT-PCR, and designated as PACHINCO (Poly (A) Capture by Hairpin Chimeric Oligonucleotide)-RT-PCR. The new method can be applied for the comprehensive determination of poly (A) in whole cellular mRNAs with simply replacing 5' primers used for PACHINCO-RT-PR with sequences involved in the corresponding 3'UTRs of mRNA. Indeed, the method was optimized for an automatic microchip DNA electrophoresis apparatus, and the elongation of poly (A) of Per1 mRNA was identified using this system.

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • Research Products

    (4 results)

All 2014 2013

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (3 results) (of which Invited: 1 results)

  • [Journal Article] Molecular assembly of the period-cryptochrome circadian transcriptional repressor complex。2014

    • Author(s)
      Nangle, SN., Rosensweig, C., Koike, N., Tei, H., Takahashi, JS., Green, CB., Zheng, N.
    • Journal Title

      Elife

      Volume: 3

    • DOI

      10.7554/elife.03674

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] 哺乳類時計遺伝子Rev-erbαの転写制御機構の解明2014

    • Author(s)
      松浦知諒、高畑佳史、山田洋一、程 肇
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2014-11-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] 哺乳類時計遺伝子Bmal1の新規転写制御機構の解析2014

    • Author(s)
      大場祐希、松本健、高畑佳史、藤井義明、程 肇
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2014-11-26
    • Related Report
      2014 Annual Research Report
  • [Presentation] 時計遺伝子、転写・翻訳フィードバックループと概日リズム2013

    • Author(s)
      程 肇
    • Organizer
      日本時間生物学会
    • Place of Presentation
      近畿大学
    • Related Report
      2013 Research-status Report
    • Invited

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Published: 2014-07-25   Modified: 2019-07-29  

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