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Study of a fast, convenient and sensitive genotoxicity test utilizing cells lacking DNA damage response factors

Research Project

Project/Area Number 25650124
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Genetics/Chromosome dynamics
Research InstitutionNational Institute of Health Sciences

Principal Investigator

AKAGI Jun-ichi  国立医薬品食品衛生研究所, 病理部, 研究員 (60512556)

Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords損傷乗り越え複製 / 遺伝毒性試験 / 遺伝毒性試験法 / 遺伝毒性 / DNA損傷トレランス / Polη / Polι / Polκ
Outline of Final Research Achievements

Genotoxicity of environmental chemicals mainly arise from modifications of genomic DNA, such as alkylation, oxidation and adduct formation. Majority of point mutations in genomic DNA are considered to be caused as the consequence of translesion synthesis (TLS) that allows direct replication past DNA lesions. On the other hand, when TLS fails, cell survival is severely affected as a result of replication fork collapse. We have analyzed the triple knockout (TKO) mouse embryonic fibroblasts lacking three TLS DNA polymerases, Polη, Polι and Polκ. The TKO cells showed increased sensitivity to various genotoxins compared to the wild-type cells. The IC50WT/IC50TKO ratios that represent the difference of cellular sensitivity between TKO cells and the wild-type cells in 10 out of 11 genotoxins were more than 2, while that in 6 nongenotoxins were less than 2.0. Thus, the hypersensitivity of TKO cells to genotoxins is useful to evaluate genotoxicity of chemicals.

Report

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

    (3 results)

All 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (2 results)

  • [Journal Article] Excision of translesion synthesis errors orchestrates responses to helix-distorting DNA lesions2015

    • Author(s)
      Anastasia Tsaalbi-Shtylik, Cristina Ferrás, Bea Pauw, Giel Hendriks, Piya Temviriyanukul, Leone Carlée, Fabienne Calléja, Sandrine van Hees, Jun-Ichi Akagi, Shigenori Iwai, Fumio Hanaoka, Jacob G. Jansen, and Niels de Wind
    • Journal Title

      The Journal of Cell Biology

      Volume: 209 Issue: 1 Pages: 33-46

    • DOI

      10.1083/jcb.201408017

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] 損傷乗り越え型DNAポリメラーゼη・ι・κ三重欠損細胞の変異原に対する高感受性を用いた遺伝毒性検出法の検討2014

    • Author(s)
      赤木 純一, 豊田 武士, Cho Young-Man, 横井 雅幸, 大森 治夫, 花岡 文雄, 小川 久美子
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜市)
    • Year and Date
      2014-11-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] Site-specific replicative analysis of 6-4 photoproduct using a series of TLS polymerases deficient mouse cells2014

    • Author(s)
      Jun-ichi Akagi, Keiji Hashimoto, Masayuki Yokoi, Haruo Ohmori, Sigenori Iwai, Masaaki Moriya and Fumio Hanaoka
    • Organizer
      International Symposium on Xeroderma Pigmentosum and Related Diseases
    • 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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