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Functional analyses of nucleoskeleton proteins on formation of radiation-induced nuclear foci of DNA repair factors

Research Project

Project/Area Number 18K18195
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 63020:Radiation influence-related
Research InstitutionHiroshima University

Principal Investigator

Horikoshi Yasunori  広島大学, 原爆放射線医科学研究所, 助教 (00719429)

Project Period (FY) 2018-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2019: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2018: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords放射線 / DNA修復 / 細胞核構造 / 核骨格タンパク質 / 放射線被ばく / DNA二本鎖切断 / 放射線応答 / DNA損傷修復 / 核構造
Outline of Final Research Achievements

The functional connectivity between higher-order nuclear architecture and responses to radiation exposure or DNA repair mechanisms of cells has been poorly understood. In this study, we focused NuMA, one of the “nucleoskeleton” proteins, and showed its involvement in both radiation susceptibility and DNA repair. We also revealed that the phosphorylation of NuMA occurs in the early stage of DNA damage responses and then amplified. This modification is limited to the vicinity of damage sites albeit their distribution throughout the entire nucleus. Besides, we found the radiation dose-dependent reduction of NuMA proteins, suggesting the effect of radiation exposure on the higher-order nuclear architecture together with chromosome DNA.

Academic Significance and Societal Importance of the Research Achievements

細胞核高次構造と、細胞の放射線応答やDNA修復機構との、機能の関連については、これまで十分には理解されていない。本研究は、ゲノム修復という「核機能」の制御に「核構造」を担う因子が関わっている具体例を示したことで、「構造による機能制御」の新しいモデルの提唱・確立に貢献した。また、放射線被ばくによりDNA以外にも細胞核、特にその高次構造が損傷を受けうるという研究結果は、今後放射線生物学に新たな展開をもたらすものと考えている。放射線治療という観点からも新たな知見であり、将来的な応用が期待される.

Report

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

    (6 results)

All 2019 2018

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (5 results) (of which Int'l Joint Research: 2 results)

  • [Journal Article] Matrin3 promotes homologous recombinational repair by regulation of RAD51.2019

    • Author(s)
      Shi L, Sun J, Kinomura A, Fukuto A, Horikoshi Y, Tashiro S.
    • Journal Title

      J Biochem.

      Volume: 166 Issue: 4 Pages: 343-351

    • DOI

      10.1093/jb/mvz041

    • NAID

      40022023652

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] Homologous pairing during recombinational DNA repair take place within distinctive nuclear compartment.2019

    • Author(s)
      Yasunori Horikoshi, Hiroki Shima, Wataru Kobayashi, Hiroshi Ochiai, Jiying Sun, Hitoshi Kurumizaka, Tsuyoshi Ikura, Shin-ichi Tate, Kazuhiko Igarashi, Thomas Cremer, Satoshi Tashiro
    • Organizer
      EMBO Workshop Chromatin and Epigenetics
    • Related Report
      2019 Annual Research Report
    • Int'l Joint Research
  • [Presentation] ゲノム損傷依存的RAD51核内フォーカス形成の制御機構2019

    • Author(s)
      堀越 保則,孫 継英,田代 聡
    • Organizer
      第十一回「光塾」
    • Related Report
      2019 Annual Research Report
  • [Presentation] Homologous pairing during recombinational DNA repair take place within distinctive nuclear compartment2019

    • Author(s)
      Yasunori Horikoshi
    • Organizer
      EMBO Workshop Chromatin and Epigenetics
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research
  • [Presentation] ゲノム損傷依存的RAD51核内フォーカス形成の制御機構2018

    • Author(s)
      堀越 保則
    • Organizer
      第59回原子爆弾後障害研究会
    • Related Report
      2018 Research-status Report
  • [Presentation] 相同組換え修復時の相同的対合は特徴的な核内区画で起こる2018

    • Author(s)
      堀越 保則
    • Organizer
      第41回日本分子生物学会年会
    • Related Report
      2018 Research-status Report

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Published: 2018-04-23   Modified: 2021-02-19  

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