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Functional analysis of nucleostemin in pluripotent stem and tissue stem cells

Research Project

Project/Area Number 21770242
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Developmental biology
Research InstitutionKeio University

Principal Investigator

NAGAMATSU Go  Keio University, 医学部, 助教 (70453545)

Project Period (FY) 2009 – 2010
Project Status Completed (Fiscal Year 2010)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2010: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2009: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Keywords幹細胞 / 自己複製
Research Abstract

We succeeded in making the conditional Nucleostemin deficient embryonic stem cells by a consecutive targeting of two times. Upon deletion of Nucleostemin allele, stop of proliferation and cell death had found. Moreover, it was clarified that the genes that did an important working to the maintenance of the undifferentiation of the embryonic stem cell, such as Oct3/4, Nanog, and Sox2 decreased along with the Nucleostemin loss. The possibility of the inducement or maintaining of the factors that Nucleostemin is related to the above-mentioned undifferentiated maintenance is suggested from this. On the other hand when Nucleostemin was over-expressed, the up-regulation of pluripotency associated genes was observed.

Report

(3 results)
  • 2010 Annual Research Report   Final Research Report ( PDF )
  • 2009 Annual Research Report
  • Research Products

    (6 results)

All 2011

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

  • [Journal Article] A germ cell specific gene, Prmt5 works as somatic cell reprogramming2011

    • Author(s)
      Nagamatsu G, Kosaka T, Kawasumi M, Kinoshita T, Takubo K, Akiyama H, Sudo T, Kobayashi T, Oya M, Suda T.
    • Journal Title

      J Biol Chem. 286(12)

      Pages: 10641-10648

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] Ataxia-telangiectasia mutated (ATM) deficiency decreases reprogramming efficiency and leads to genomic instabilityin iPS cells.2011

    • Author(s)
      Kinoshita T, Nagamatsu G, Kosaka T, Takubo K, Hotta A, Ellis J, Suda T.
    • Journal Title

      Biochem Biophys Res Commun. 407(2)

      Pages: 321-326

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] A germ cell specific gene, Prmt5 works as somatic cell reprogramming2011

    • Author(s)
      Nagamatsu G, Kosaka T, Kawasumi M, Kinoshita T, Takubo K, Akiyama H, Sudo T, Kobayashi T, Oya M, Suda T.
    • Journal Title

      J Biol Chem.

      Volume: 286(12) Pages: 10641-8

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Ataxia-telangiectasia mutated (ATM) deficiency decreases reprogramming efficiency and leads to genomic instability in iPS cells.2011

    • Author(s)
      Kinoshita T, Nagamatsu G, Kosaka T, Takubo K, Hotta A, Ellis J, Suda T.
    • Journal Title

      Biochem Biophys Res Commun.

      Volume: 407(2) Pages: 321-6

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Presentation] 始原生殖細胞からの多能性幹細胞分化2011

    • Author(s)
      永松剛・小坂威雄・田久保圭誉・大家基嗣・須田年生
    • Organizer
      第10回日本再生医療学会総会
    • Place of Presentation
      京王プラザホテル(新宿)
    • Year and Date
      2011-03-02
    • Related Report
      2010 Final Research Report
  • [Presentation] 始原生殖細胞からの多能性幹細胞分化2011

    • Author(s)
      永松剛・小坂威雄・田久保圭誉・大家基嗣・須田年生
    • Organizer
      第10回 日本再生医療学会総会
    • Place of Presentation
      京王プラザホテル(新宿)
    • Year and Date
      2011-03-02
    • Related Report
      2010 Annual Research Report

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Published: 2009-04-01   Modified: 2016-04-21  

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