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Functional analysis of Jmjd5, a candidate cancer-related geneidentified by retroviral insertional mutagenesis

Research Project

Project/Area Number 23790220
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field General anatomy (including Histology/Embryology)
Research InstitutionKanazawa University

Principal Investigator

ISHIMURA Akihiko  金沢大学, がん進展制御研究所, 助教 (80375261)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2011: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Keywords遺伝子発現 / 発生・分化 / 細胞増殖 / 癌 / がん / ヒストンメチル化修飾 / マウス胚発生
Research Abstract

Our retroviral insertional mutagenesis in mice showed frequent identification of JmjC family genes as novel candidates cancer-related genes. Jmjd5, one of the family genes, was also a target for the retrovirus, and we generated Jmjd5-deficientmice (Jmjd5△囗△) to investigate the physiological role of Jmjd5. We showed that Jmjd5 was involved in embryonic cell proliferation by fine-tuning the expression of p21 (Ishimura et al., Development 2012).

Report

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

    (13 results)

All 2013 2012 2011 Other

All Journal Article (4 results) (of which Peer Reviewed: 4 results) Presentation (9 results)

  • [Journal Article] Jmjd5, an H3K36me2 histone demethylase, modulates embryonic cell proliferation through the regulation of Cdknla expression2012

    • Author(s)
      Ishimura, A., K-I. Minehata, M.Terashima, G.Kondoh, T.Hara, T. Suzuki
    • Journal Title

      Development

      Volume: 139 Issue: 4 Pages: 749-759

    • DOI

      10.1242/dev.074138

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Jmjd5, an H3K36me2 histone demethylase, modulates embryonic cell proliferation through the regulation of Cdkn1a expression.2012

    • Author(s)
      Ishimura A.
    • Journal Title

      Development

      Volume: 139 Pages: 749-759

    • Related Report
      2011 Research-status Report
    • Peer Reviewed
  • [Journal Article] PLU1 histone demethylase decreases the expression of KAT5 and enhances the invasive activity of the cells2011

    • Author(s)
      Yoshida M, Ishimura A, Terashima M, Enkhbaatar Z, Nozaki N, Satou K, Suzuki T
    • Journal Title

      Biochemical J.

      Volume: 43 Issue: 3 Pages: 555-564

    • DOI

      10.1042/bj20110343

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] PLU1 histone demethylase decreases the expression of KAT5 and enhances the invasive activity of the cells.2011

    • Author(s)
      Yoshida M.
    • Journal Title

      Biochemical Journal

      Volume: 437 Pages: 555-564

    • Related Report
      2011 Research-status Report
    • Peer Reviewed
  • [Presentation] Jmjd5, a JmjC domain containing protein, modulates embryonic cell proliferation through the regulation of p53-target genes expression2013

    • Author(s)
      Ishimura A
    • Organizer
      3rdInternational Symposium on Carcinogenic Spiral and International Symposium in Tumor Biology in Kanazawa
    • Place of Presentation
      金沢東急エクセルホテル(石川県)
    • Year and Date
      2013-01-25
    • Related Report
      2012 Final Research Report
  • [Presentation] Jmjd5, an H3K36me2 histone demethylase, modulates embryonic cell proliferation through the regulation of p53-target genes expression2012

    • Author(s)
      Ishimura A, Minehata K, Terashima M, Kondoh G, Hara T and Suzuki T
    • Organizer
      第35回分子生物学学会年会
    • Place of Presentation
      福岡国際会議場(福岡県)
    • Year and Date
      2012-12-13
    • Related Report
      2012 Final Research Report
  • [Presentation] Jmjd5, which is identified by retroviral insertional mutagenesis, regulates embryonic cell proliferation through the epigenetic control of Cdkn1a2011

    • Author(s)
      Ishimura A, Minehata K, Terashima M, Kondoh G, Hara T and Suzuki T
    • Organizer
      第34回分子生物学学会年会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2011-12-13
    • Related Report
      2012 Final Research Report
  • [Presentation] Jmjd5, a candidate cancere-related gene identified by retroviral insertional mutagenesis, regulates the expression of Cdkn1a and modulates embryonic cell proliferation2011

    • Author(s)
      Ishimura A, Minehata K, Terashima M, Hara T and Suzuki T
    • Organizer
      International Symposium on Tumor Biology in Kanazawa and the 11thSpring Symposium of the Molecular Biology Society of Japan
    • Place of Presentation
      石川県立音楽堂(石川県)
    • Year and Date
      2011-05-25
    • Related Report
      2012 Final Research Report
  • [Presentation] Jmjd5, which is identified by retroviral insertional mutagenesis, regulates embryonic cell proliferation through the epigenetic control of Cdkn1a.2011

    • Author(s)
      Ishimura A.
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Related Report
      2011 Research-status Report
  • [Presentation] Jmjd5, which is identified by retroviral insertional mutagenesis, regulates Cdkn1a and modulates embryonic cell growth.2011

    • Author(s)
      Ishimura A.
    • Organizer
      第70回日本癌学会学術総会
    • Place of Presentation
      名古屋国際会議場(愛知県)
    • Related Report
      2011 Research-status Report
  • [Presentation] Jmjd5, a candidate cancer-related gene identified by retroviral insertional mutagenesis, regulates the expression of Cdkn1a and modulates embryonic cell proliferation.2011

    • Author(s)
      Ishimura A.
    • Organizer
      International Symposium on Tumor Biology in Kanazawa and the 11th Spring Symposium of the Molecular Biology Society of Japan
    • Place of Presentation
      石川県立音楽堂(石川県)
    • Related Report
      2011 Research-status Report
  • [Presentation] Jmjd5, a JmjC domain containing protein, modulates embryonic cell proliferation through the regulation of p53-target genes expression.

    • Author(s)
      Ishimura A
    • Organizer
      3rd International Symposium on Carcinogenic Spiral and International Symposium in Tumor Biology in Kanazawa.
    • Place of Presentation
      金沢東急エクセルホテル ( 石川県)
    • Related Report
      2012 Annual Research Report
  • [Presentation] Jmjd5, an H3K36me2 histone demethylase, modulates embryonic cell proliferation through the regulation of p53-target genes expression.

    • Author(s)
      Ishimura A
    • Organizer
      第35回分子生物学学会年会
    • Place of Presentation
      福岡国際会議場 ( 福岡県)
    • Related Report
      2012 Annual Research Report

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

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