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Development of method for analysis of long non-coding RNA by combination of DNAzyme, solid-phase DNA probe and mass spectrometry

Research Project

Project/Area Number 18K19302
Research Category

Grant-in-Aid for Challenging Research (Exploratory)

Allocation TypeMulti-year Fund
Review Section Medium-sized Section 43:Biology at molecular to cellular levels, and related fields
Research InstitutionEhime University

Principal Investigator

HORI Hiroyuki  愛媛大学, 理工学研究科(工学系), 教授 (20256960)

Co-Investigator(Kenkyū-buntansha) 横川 隆志  岐阜大学, 工学部, 教授 (90242304)
Project Period (FY) 2018-06-29 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥6,240,000 (Direct Cost: ¥4,800,000、Indirect Cost: ¥1,440,000)
Fiscal Year 2019: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
Fiscal Year 2018: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
Keywords核酸 / 酵素 / RNA / タンパク質 / 質量分析
Outline of Final Research Achievements

In RNA sequencing with modified nucleosides, the most reliable method is mass spectrometry. In general, the target RNA is digested with ribonuclease (RNase) and then the fragments are analyzed by mass spectrometry. In the case of long non-coding RNAs, however, cleavage by ribonucleases often generates duplicated RNA fragments, which possess the same sequence. Therefore, the difficulty of analysis of long non-coding RNAs by MS spectrometry rises with increasing length of RNA. To overcome this problem, we developed a method for analysis of long non-coding RNA. In the method, long non-coding RNA is site-specifically cleaved by deoxyribozyme (DNAzyme) and then its fragments are purified by the solid-phase DNA probe method. The sequence of RNA fragment is determined by mass spectrometry.

Academic Significance and Societal Importance of the Research Achievements

RNA中には、メチル化されたものやアセチル化されたものなど、様々な修飾ヌクレオシドが含まれます。これら修飾ヌクレオシドは、タンパク質合成系を制御し、発生・分化、発がん、感染、免疫など高次生命現象ともリンクします。従って、どのようなRNAの、どこに、どんな修飾ヌクレオシドが、どのくらいの頻度で存在するのかを調べるのは、現代の生命科学で重要な課題となっています。しかしながら、既存の手法のみで、長鎖RNAの修飾を調べるのは容易ではありません。本研究では、新たな手法を開発しました。この研究成果は、単に分子生物学・生化学分野のみにとどまらず、医学、薬学、農学、理学、工学等、多方面に波及するものです。

Report

(3 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • Research Products

    (6 results)

All 2020 2019 2018 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (3 results) Remarks (2 results)

  • [Journal Article] Application of solid-phase DNA probe method with cleavage by deoxyribozyme for analysis of long non-coding RNAs2020

    • Author(s)
      Arakawa, S., Kamizaki, K., Kuwana, Y., Kataoka, N., Naoe, C., Takemoto, C., Yokogawa, T., and Hori, H.
    • Journal Title

      Journal of Biochemistry

      Volume: in press

    • NAID

      40022375426

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed
  • [Presentation] デオキシリボザイムと固相化DNAプローブ法を併用したRNA断片精製法の開発2019

    • Author(s)
      荒川静花, 上崎晃輔, 堀 弘幸
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] 高度好熱菌16S rRNAのアンチ・シャイン・ダルガーノ配列領域に存在する2つのシュードウリジンの合成酵素の探索2019

    • Author(s)
      上崎晃輔, 荒川静花, 桑名祐輔, 白水美香子, 竹本千重, 堀 弘幸
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] DNAザイム切断、固相化DNAプローブ法を併用したThermus thermophilus rRNA中のシュードウリジンの分析2018

    • Author(s)
      上崎晃輔、荒川静花、白水美香子、竹本千重、堀 弘幸
    • Organizer
      第41回日本分子生物学会年会
    • Related Report
      2018 Research-status Report
  • [Remarks]

    • URL

      http://www.ach.ehime-u.ac.jp/bchem/

    • Related Report
      2019 Annual Research Report
  • [Remarks] 応用生物化学研究室ホームページ

    • URL

      http://www.ach.ehime-u.ac.jp/bchem/

    • Related Report
      2018 Research-status Report

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Published: 2018-07-25   Modified: 2021-02-19  

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