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Study on the splicing checkpoint mechanism to prevent pre-mRNA accumulation caused by splicing abnormality

Research Project

Project/Area Number 25711001
Research Category

Grant-in-Aid for Young Scientists (A)

Allocation TypePartial Multi-year Fund
Research Field Molecular biology
Research InstitutionUniversity of Toyama

Principal Investigator

Kaida Daisuke  富山大学, 大学院医学薬学研究部(医学), 准教授 (60415122)

Project Period (FY) 2013-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥26,780,000 (Direct Cost: ¥20,600,000、Indirect Cost: ¥6,180,000)
Fiscal Year 2016: ¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2015: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥10,920,000 (Direct Cost: ¥8,400,000、Indirect Cost: ¥2,520,000)
Keywordsスプライシング / 転写 / RNAポリメラーゼII
Outline of Final Research Achievements

mRNA splicing is a fundamental mechanism for the gene expression in eukaryotes. Splicing abnormality might cause pre-mRNA accumulation and diseases. Therefore, I assumed that cells have a checkpoint mechanism that detects splicing abnormality and suppresses transcriptional elongation to prevent pre-mRNA accumulation. I revealed that such a splicing checkpoint mechanism actually exists in this study.

Report

(5 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Annual Research Report
  • 2014 Annual Research Report
  • 2013 Annual Research Report
  • Research Products

    (17 results)

All 2017 2016 2015 2014 2013

All Journal Article (4 results) (of which Peer Reviewed: 4 results,  Open Access: 3 results,  Acknowledgement Compliant: 2 results) Presentation (12 results) (of which Int'l Joint Research: 1 results,  Invited: 4 results) Book (1 results)

  • [Journal Article] Upregulation of p27 cyclin-dependent kinase inhibitor and a C-terminus truncated form of p27 contributes to G1 phase arrest2016

    • Author(s)
      Takayuki Satoh, Daisuke Kaida
    • Journal Title

      Scientific Reports

      Volume: 6 Issue: 1 Pages: 27829-27829

    • DOI

      10.1038/srep27829

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] The reciprocal regulation between splicing and 3′‐end processing2016

    • Author(s)
      Daisuke Kaida
    • Journal Title

      Wiley Interdisciplinary Reviews: RNA

      Volume: 7 Issue: 4 Pages: 499-511

    • DOI

      10.1002/wrna.1348

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Splicing inhibition decreases phosphorylation level of Ser2 in Pol II CTD2015

    • Author(s)
      Mitsunori Koga, Megumi Hayashi and Daisuke Kaida
    • Journal Title

      Nucleic Acids Research

      Volume: 43 Issue: 17 Pages: 8258-8267

    • DOI

      10.1093/nar/gkv740

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] U2 snRNP is required for expression of the 3' end of genes2014

    • Author(s)
      Koga, M., Satoh, T., Takasaki, I., Kawamura, Y., Yoshida, M., and Kaida, D
    • Journal Title

      PloS One

      Volume: 9 Issue: 5 Pages: e98015-e98015

    • DOI

      10.1371/journal.pone.0098015

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Presentation] 細胞の正常な機能を維持するmRNAスプライシングチェックポイント機構2017

    • Author(s)
      甲斐田大輔
    • Organizer
      富山RNAワークショップ
    • Place of Presentation
      富山大学
    • Year and Date
      2017-03-13
    • Related Report
      2016 Annual Research Report
    • Invited
  • [Presentation] 細胞の正常な機能を維持するmRNAスプライシングチェックポイント機構2017

    • Author(s)
      甲斐田大輔
    • Organizer
      第3回バイオシグナル研究会
    • Place of Presentation
      神戸大学
    • Year and Date
      2017-03-08
    • Related Report
      2016 Annual Research Report
    • Invited
  • [Presentation] スプライシング阻害剤スプライソスタチンAは転写活性と細胞周期進行を制御する2015

    • Author(s)
      甲斐田大輔
    • Organizer
      第38回 日本分子生物学会年会
    • Place of Presentation
      神戸
    • Year and Date
      2015-12-01
    • Related Report
      2015 Annual Research Report
    • Invited
  • [Presentation] mRNAスプライシングの異常はPol II Ser2の脱リン酸化を引き起こす2015

    • Author(s)
      古賀光徳、甲斐田大輔
    • Organizer
      第2回北陸エピジェネティクス研究会
    • Place of Presentation
      富山
    • Year and Date
      2015-11-11
    • Related Report
      2015 Annual Research Report
  • [Presentation] Splicing inhibition decreases phosphorylation level of Pol II CTD Ser22015

    • Author(s)
      Daisuke Kaida and Mitsunori Koga
    • Organizer
      RNA 2015 The 20th Annual Meeting of the RNA Society
    • Place of Presentation
      Madison, WI, USA
    • Year and Date
      2015-05-25
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research
  • [Presentation] スプライシング活性はPol II Ser2のリン酸化と転写伸長に必要である2014

    • Author(s)
      古賀光徳, 佐藤崇之, 甲斐田大輔
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2014-11-25 – 2014-11-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] mRNA splicing activity is required for efficient transcription elongation2014

    • Author(s)
      甲斐田大輔
    • Organizer
      RIKEN Symposium/15th Tokyo RNA Club “Noncoding RNA regulation“
    • Place of Presentation
      埼玉
    • Year and Date
      2014-10-01
    • Related Report
      2014 Annual Research Report
    • Invited
  • [Presentation] スプライシング活性はPol II Ser2のリン酸化と転写伸長に必要である2014

    • Author(s)
      古賀光徳, 佐藤崇之, 甲斐田大輔
    • Organizer
      第16回日本RNA学会年会
    • Place of Presentation
      名古屋
    • Year and Date
      2014-07-23 – 2014-07-25
    • Related Report
      2014 Annual Research Report
  • [Presentation] U2 snRNP is required for transcription elongation in a gene specific manner.2014

    • Author(s)
      古賀光徳, 佐藤崇之, 甲斐田大輔
    • Organizer
      RNA 2014 The 19th Annual Meeting of the RNA Society
    • Place of Presentation
      Quebec, Canada
    • Year and Date
      2014-06-03 – 2014-06-08
    • Related Report
      2014 Annual Research Report
  • [Presentation] U2 snRNP is required for the phosphorylation of Pol II CTD and efficient transcription elongation.2014

    • Author(s)
      古賀光徳, 佐藤崇之, 甲斐田大輔
    • Organizer
      2014 American Society for Biochemistry and Molecular Biology Annual Meeting
    • Place of Presentation
      San Diego, CA, USA
    • Year and Date
      2014-04-26 – 2014-04-30
    • Related Report
      2014 Annual Research Report
  • [Presentation] スプライシング異常はP-TEFbを阻害することで転写伸長抑制を引き起こす2013

    • Author(s)
      古賀光徳、甲斐田大輔
    • Organizer
      日本RNA学会年会
    • Place of Presentation
      愛媛県県民文化会館
    • Related Report
      2013 Annual Research Report
  • [Presentation] U2 snRNP is required for the phosphorylation of CTD Ser2 and efficient transcription elongation2013

    • Author(s)
      Daisuke Kaida, Mitsunori Koga
    • Organizer
      Cold Spring Harbor Laboratory meeting “Eukaryotic mRNA processing”
    • Place of Presentation
      Cold Spring Harbor Laboratory
    • Related Report
      2013 Annual Research Report
  • [Book] ノンコーディングRNA2016

    • Author(s)
      甲斐田大輔
    • Total Pages
      355
    • Publisher
      化学同人
    • Related Report
      2016 Annual Research Report

URL: 

Published: 2013-05-21   Modified: 2019-07-29  

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