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A novel type of cell death in tetraploids with chromosomal aberrations

Research Project

Project/Area Number 24657132
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Cell biology
Research InstitutionKyoto University

Principal Investigator

YONEHARA Shin  京都大学, 生命科学研究科, 教授 (00124503)

Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords細胞死 / 二核四倍体細胞 / eEF1A1
Research Abstract

Abnormal chromosomal condensation induces binuclear cells with a genetically unstable tetraploidy known to facilitate aneuploid malignancies. We found such binuclear tetraploid cells to be eliminated by a novel type of programmed cell death in Chinese hamster cells. To enable various analyses of the novel cell death, we established human and mouse cell lines where the novel cell death can be induced, and then obtained exhaustive gene expression profiles from human cells before and after induction of the cell death. We found that induction of the cell death was mediated by down-regulated expression of eEF1A1 protein through accumulation of eEF1A1 mRNA into P bodies (Processing bodies), and the binding of CNBP protein to eEF1A1 mRNA was involved in this process.

Report

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

    (11 results)

All 2013 2012 Other

All Journal Article (5 results) (of which Peer Reviewed: 5 results) Presentation (2 results) (of which Invited: 2 results) Remarks (4 results)

  • [Journal Article] Identification of a mechanism that couples multisite phosphorylation of Yes-Associated Protein (YAP) with transcriptional coactivation and regulation of apoptosis.2013

    • Author(s)
      Lee KK, Yonehara S
    • Journal Title

      Journal of Biological Chemistry

      Volume: 287 Issue: 12 Pages: 9568-9578

    • DOI

      10.1074/jbc.m111.296954

    • Related Report
      2013 Annual Research Report 2013 Final Research Report 2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Dclk1 distinguishes between tumor and normal stem cells in the intestine.2013

    • Author(s)
      Yuki Nakanishi, et. al.
    • Journal Title

      Nature Genetics

      Volume: 45 Issue: 1 Pages: 98-103

    • DOI

      10.1038/ng.2481

    • Related Report
      2013 Annual Research Report 2013 Final Research Report 2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Fas deficiency in mice with the Balb/c background induces blepharitis with allergic inflammation and hyper-IgE production in conjunction with severe autoimmune disease.2013

    • Author(s)
      Takahashi S
    • Journal Title

      Int Immunol

      Volume: 25 Issue: 5 Pages: 287-293

    • DOI

      10.1093/intimm/dxs109

    • Related Report
      2013 Final Research Report 2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Identification of a novel type 2 innate immunocyte with ability to enhance IgE production.2013

    • Author(s)
      Fukuoka A
    • Journal Title

      Int Immunol

      Volume: 25 Issue: 6 Pages: 373-382

    • DOI

      10.1093/intimm/dxs160

    • Related Report
      2013 Final Research Report 2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Protease activity of procaspase-8 is essential for cell survival by inhibiting both apoptotic and nonapoptotic cell death dependent on receptor interacting protein kinase 1 (RIP1) and RIP3.2012

    • Author(s)
      Kikuchi M
    • Journal Title

      J Boil Chem

      Volume: 287 Issue: 49 Pages: 41165-41173

    • DOI

      10.1074/jbc.m112.419747

    • Related Report
      2013 Annual Research Report 2013 Final Research Report 2012 Research-status Report
    • Peer Reviewed
  • [Presentation] Fasとcaspase-8の新しい生理・病理機能2013

    • Author(s)
      米原伸
    • Organizer
      第22回日本Cell Death学会学術集会特別講演
    • Place of Presentation
      京都市
    • Related Report
      2013 Final Research Report
    • Invited
  • [Presentation] Fasとcaspase-8の新しい生理・病理機能2013

    • Author(s)
      米原 伸
    • Organizer
      第22回 日本Cell Death学会 学術集会 特別講演
    • Place of Presentation
      京都市
    • Related Report
      2013 Annual Research Report
    • Invited
  • [Remarks] 米原研究室ホームページ:研究内容や研究業績を記載

    • URL

      http://www.lif.kyoto-u.ac.jp/labs/Fas/Home_j.htm

    • Related Report
      2013 Final Research Report
  • [Remarks] 京都大学生命科学研究科高次遺伝情報学研究分野(米原研究室ホームページ):研究内容や研究業績を記載

    • URL

      http://www.lif.kyoto-u.ac.jp/labs/Fas/Home_j.htm

    • Related Report
      2013 Annual Research Report
  • [Remarks] 京都大学大学院 生命科学研究科 高次遺伝情報学分野

    • URL

      http://www.lif.kyoto-u.ac.jp/labs/Fas/Home_j.htm

    • Related Report
      2012 Research-status Report
  • [Remarks] 京都大学大学院生命科学研究科

    • URL

      http://www.lif.kyoto-u.ac.jp/j/

    • Related Report
      2012 Research-status Report

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Published: 2013-05-31   Modified: 2019-07-29  

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