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RNase H2 is essential for ribonucleotide excision repair during DNA replication

Research Project

Project/Area Number 25650028
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Functional biochemistry
Research InstitutionUniversity of Tsukuba

Principal Investigator

KASHIWABARA Shin-ichi  筑波大学, 生命環境系, 准教授 (00254318)

Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywordsリボヌクレオチド除去修復 / ゲノム安定性 / RNase H2
Outline of Final Research Achievements

RNase H2 is an enzyme capable of cleaving the 5’-phosphodiester bond of single ribonucleotides (rNMPs) embedded in RNA/DNA heteroduplexes. Embryos homozygous for the targeted mutation of Rnaseh2a gene exhibited gross apoptosis and failed to develop beyond E10.5. Chromosomal DNA from mutant embryos contained numerous rNMPs. Expression of DNA damage response genes, including cyclin G1 and p21, was up-regulated by the absence of RNase H2. It was also found that the enzyme is essential for normal cell proliferation via correct chromosomal DNA replication but is dispensable for cell survival. These results indicate that RNase H2 is a key enzyme responsible for eliminating rNMPs misincorporated during DNA replication, thereby ensuring genome stability and normal cell proliferation.

Report

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

    (6 results)

All 2014 Other

All Presentation (6 results)

  • [Presentation] Polyadenylation activity of testis-specific poly(A) polymerase, TPAP/PAPOLB, is essential for spermatogenesis2014

    • Author(s)
      鶴田皐月、柏原真一、岡田渓太郎、山岡悠太郎、馬場 忠
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2014-11-25 – 2014-11-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] Mechanism of translational repression by germ cell-specific Y-box RNA-binding proteins, MSY2 and MSY42014

    • Author(s)
      三枝彩佳、柏原真一、岡田渓太郎、馬場 忠
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2014-11-25 – 2014-11-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] Characterization of translation- and PABPC-dependent deadenylation intermediates2014

    • Author(s)
      岡田渓太郎、柏原真一、三枝彩佳、鶴田皐月、馬場 忠
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2014-11-25 – 2014-11-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] 翻訳に伴い生成されるmRNA脱アデニル化中間体の解析2014

    • Author(s)
      岡田渓太郎、柏原真一、三枝彩佳、鶴田皐月、馬場 忠
    • Organizer
      第16回日本RNA学会年会
    • Place of Presentation
      ウインクあいち(名古屋)
    • Year and Date
      2014-07-23 – 2014-07-25
    • Related Report
      2014 Annual Research Report
  • [Presentation] マウス生殖細胞特異的Y-box RNA結合タンパク質の機能解析2014

    • Author(s)
      三枝彩佳、柏原真一、馬場 忠
    • Organizer
      第16回日本RNA学会年会
    • Place of Presentation
      ウインクあいち(名古屋)
    • Year and Date
      2014-07-23 – 2014-07-25
    • Related Report
      2014 Annual Research Report
  • [Presentation] 半数体特異的mRNAの翻訳と脱アデニル化との関連

    • Author(s)
      岡田渓太郎、柏原真一、三枝彩佳、馬場 忠
    • Organizer
      第36回日本分子生物学会年会
    • Place of Presentation
      神戸国際会議場
    • Related Report
      2013 Research-status Report

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

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