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Molecular mechanism for arrested fork stabilization by fork recognition complex

Research Project

Project/Area Number 23570183
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Functional biochemistry
Research InstitutionTokyo Metropolitan Institute of Medical Science

Principal Investigator

TANAKA Taku  公益財団法人東京都医学総合研究所, ゲノム医科学研究分野, 主席研究員 (80425686)

Project Period (FY) 2011 – 2013
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
KeywordsDNA複製 / 複製起点 / 複製再開始 / マイクロアレイ / PriA / RecA / 複製フォーク / フォーク安定化因子 / DNA結合 / 修復・組換え / 分子間相互作用
Research Abstract

Analyses for arrested replication fork recognition by fork stabilizing factor are important for elucidation of molecular mechanism of replication restart reaction. Escherichia coli PriA protein, bacterial fork stabilizing factor which can bind to arrested replication forks, can be used as an indicator for detection of arrested forks in living cells. PriA binds to novel replication origin and replication restart, which is activated by origin-independent system, depends on formation of RNA-DNA hybrid. RNA-dependent initiation system for replication may reflect primitive replication mechanism and these findings shed light on evolution of eukaryotic replication system.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (5 results)

All 2013 2012 2011 Other

All Presentation (5 results)

  • [Presentation] PriA binds to oriC segments upon induction of fork stall in Escherichia coli cells2013

    • Author(s)
      Tanaka, T. and Masai, H.
    • Organizer
      第36回日本分子生物学会
    • Place of Presentation
      神戸
    • Year and Date
      2013-12-04
    • Related Report
      2013 Final Research Report
  • [Presentation] Toward the elucidation of molecular basis of kinase activation and substrate recognition of Cdc7-Dbf4 kinase complex : use of Microsporidia as a model2012

    • Author(s)
      Iwasaki, R., Tanaka, T. Shimada, A., Kohda, D., and Masai, H.
    • Organizer
      第35回日本分子生物学会
    • Place of Presentation
      福岡
    • Year and Date
      2012-12-12
    • Related Report
      2013 Final Research Report
  • [Presentation] Detection of chromosomal fragile sites : application of specific PriA binding to arrested replication forks in living cells2011

    • Author(s)
      Tanaka, T. and Masai, H.
    • Organizer
      第34回日本分子生物学会
    • Place of Presentation
      横浜
    • Year and Date
      2011-12-15
    • Related Report
      2013 Final Research Report
  • [Presentation] Detection of chromosomal fragile sites: application of specific PriA binding to arrested replication forks in living cells.2011

    • Author(s)
      田中 卓、正井 久雄
    • Organizer
      第34回日本分子生物学会
    • Place of Presentation
      横浜
    • Related Report
      2011 Research-status Report
  • [Presentation] PriA binds to oriC segments upon induction of fork stall in Escherichia coli cells

    • Author(s)
      田中 卓、正井 久雄
    • Organizer
      第36回日本分子生物学会
    • Place of Presentation
      神戸
    • Related Report
      2013 Annual Research Report

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Published: 2011-08-05   Modified: 2019-07-29  

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