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Functional analysis of cohesin during CNS development

Research Project

Project/Area Number 24890114
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Cerebral neurosurgery
Research InstitutionOsaka University

Principal Investigator

FUJITA Yuki  大阪大学, 医学(系)研究科(研究院), 特任助教 (常勤) (60631215)

Project Period (FY) 2012-08-31 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2013: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2012: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords中枢神経
Research Abstract

Cohesin complex is composed of four subunits, Smc3, Smc1, Scc3, and Scc1, and has a role in sister chromatid cohesion, which is crucial for accurate chromosome segregation. Cohesin is also known to be involved in chromatin organization by forming chromatin loops at particular loci and regulate gene expression in postmitotic cells. Disruption of cohesin network results in cohesinopathies such as Cornelia de Lange syndrome. These diseases cause higher brain dysfunction, suggesting the role of cohesin in gene regulation rather than chromosome segregation. In this study, we tested the hypothesis that cohesin regulates genome organization and its deficiency leads to higher brain dysfunction.

Report

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

    (9 results)

All 2014 2013 Other

All Journal Article (1 results) Presentation (7 results) Remarks (1 results)

  • [Journal Article] Brimonidine promotes axon growth after optic nerve injury through Erk phosphorylation2013

    • Author(s)
      Fujita, Y., Sato, A. and Yamashita
    • Journal Title

      Cell Death Dis

      Volume: 4

    • Related Report
      2013 Final Research Report
  • [Presentation] 中枢神経発生・発達におけるSMC3タンパク質の役割2014

    • Author(s)
      藤田幸、山下俊英
    • Organizer
      第119回日本解剖学会総会・全国学術集会
    • Place of Presentation
      栃木県下野市自治医科大学キャンパス
    • Related Report
      2013 Final Research Report
  • [Presentation] Functional analysis of SMC3 +/- mouse2014

    • Author(s)
      藤田幸
    • Organizer
      International symposium "New Frontier of Molecular Neuropathology 2014"
    • Place of Presentation
      御茶ノ水
    • Related Report
      2013 Annual Research Report
  • [Presentation] 中枢神経発生・発達におけるSMC3タンパク質の役割2014

    • Author(s)
      藤田幸
    • Organizer
      第119回 日本解剖学会総会・全国学術集会
    • Place of Presentation
      下野
    • Related Report
      2013 Annual Research Report
  • [Presentation] コヒーシン欠損による神経新生の抑制Neuro20132013

    • Author(s)
      藤田幸、坂東優篤、白髭克彦、山下俊英
    • Organizer
      第36回日本神経科学大会,第56回日本神経化学会大会,第23回日本神経回路学会大会
    • Place of Presentation
      京都府京都市国立京都国際会館
    • Related Report
      2013 Final Research Report
  • [Presentation] Identification of a novel binding partner of SIRT1 in neurons Neuro20132013

    • Author(s)
      藤原慧、藤田幸、山下俊英
    • Organizer
      第36回日本神経科学大会,第56回日本神経化学会大会,第23回日本神経回路学会大会
    • Place of Presentation
      京都府京都市国立京都国際会館
    • Related Report
      2013 Final Research Report
  • [Presentation] コヒーシン欠損による神経新生の抑制2013

    • Author(s)
      藤田幸
    • Organizer
      Neuro2013
    • Place of Presentation
      京都
    • Related Report
      2013 Annual Research Report
  • [Presentation] 染色体高次構造変化による中枢神経の分化・発生異常2013

    • Author(s)
      藤田幸
    • Organizer
      第14回 ORIGIN 神経科学研究会 夏のワークショップ
    • Place of Presentation
      岐阜
    • Related Report
      2013 Annual Research Report
  • [Remarks]

    • URL

      http://www.med.osaka-u.ac.jp/pub/molneu/index.html

    • Related Report
      2013 Final Research Report

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Published: 2012-11-27   Modified: 2019-07-29  

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