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Roles of E3 ubiquitin ligase RNF168 as an adaptor molecule for histone H3 methylation

Research Project

Project/Area Number 25550028
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Risk sciences of radiation and chemicals
Research InstitutionOsaka University

Principal Investigator

Nakada Shinichiro  大阪大学, 医学(系)研究科(研究院), 准教授 (70548528)

Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2014: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2013: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
KeywordsDNA修復 / DNA2本鎖切断 / DNA損傷応答 / DNA損傷 / RNF168 / 53BP1
Outline of Final Research Achievements

53BP1 localizes to sites of DNA double-strand breaks (DSBs) and protects the DSB ends from degradation. Since the localization of 53BP1 to DSB sites depends on E3 ubiquitin ligase RNF168, we investigated the molecular mechanism how RNF168 regulates the 53BP1 accumulation at DSB sites. Our data suggest that RNF168 forms protein complex with BAT3 and DOT1L and these proteins also regulate the localization of 53BP1 to DSB sites. Even though other data implicate that contribution of the function of RNF168 as an adaptor is partial, RNF168 can works as an adaptor for the localization of DOT1L to DSB sites. Our data also suggest that RNF168 localizes to DSB sites by a mechanism that has not been reported yet.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (6 results)

All 2015 2014 Other

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

  • [Presentation] 相同組換え修復過程におけるユビキチン化の関与2015

    • Author(s)
      中田慎一郎
    • Organizer
      第38回日本分子生物学会年会・第88回日本生化学会合同大会
    • Place of Presentation
      神戸
    • Year and Date
      2015-12-01
    • Related Report
      2015 Annual Research Report
    • Invited
  • [Presentation] DNA damage-induced Ubiquitination Affects DNA Repair Pathway Choice.2015

    • Author(s)
      Shinichiro Nakada
    • Organizer
      15th International Congress of Radiation Research
    • Place of Presentation
      京都
    • Year and Date
      2015-05-25
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] ユビキチン依存性DNA2本鎖損傷応答シグナルとDNA修復2014

    • Author(s)
      中田慎一郎
    • Organizer
      分子生物学会
    • Place of Presentation
      横浜
    • Year and Date
      2014-11-25 – 2014-11-27
    • Related Report
      2014 Research-status Report
    • Invited
  • [Presentation] ユビキチン化制御によるDNA2本鎖損傷修復選択機構2014

    • Author(s)
      中田慎一郎
    • Organizer
      放射線影響学会
    • Place of Presentation
      鹿児島
    • Year and Date
      2014-10-01 – 2014-10-03
    • Related Report
      2014 Research-status Report
    • Invited
  • [Remarks] 大阪大学大学院 医学系研究科 細胞応答制御学

    • URL

      http://www.bcr.med.osaka-u.ac.jp/public_html/index.html

    • Related Report
      2015 Annual Research Report
  • [Remarks] 大阪大学大学院医学系研究科細胞応答制御学

    • URL

      http://www.bcr.med.osaka-u.ac.jp/public_html/index.html

    • Related Report
      2013 Research-status Report

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

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