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Regulation of intercellular crosstalk by induced ubiquitin ligase SSB

Research Project

Project/Area Number 25860043
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Biological pharmacy
Research InstitutionNagoya University

Principal Investigator

FUMIHIKO Okumura  名古屋大学, 理学(系)研究科(研究院), 助教 (00507212)

Co-Investigator(Renkei-kenkyūsha) 嘉村 巧   (40333455)
Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2013: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywordsユビキチン / ガン / タンパク質分解
Outline of Final Research Achievements

The aim is to identify the molecular mechanism which regulates intercellular crosstalk by SOCS box protein SSB.
We identified SSB-binding proteins. Given that SSB is a ubiquitin ligase, we checked the stability of SSB-binding proteins and found that one of the candidate accumulated by knockdown of SSB. The candidate has been reported as a tumor suppressor gene and also as a oncogene. We are currently studying the physiological function of the candidate protein.

Report

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

    (4 results)

All 2014 2013

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (3 results)

  • [Journal Article] The nutrient stress-induced small GTPase Rab5 contributes to the activation of vesicle trafficking and vacuolar activity.2014

    • Author(s)
      Nakatsukasa K, Kanada A, Matsuzaki M, Byrne SD, Okumura F, Kamura T.
    • Journal Title

      J Biol Chem.

      Volume: 289(30) Pages: 20970-20978

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed
  • [Presentation] pVHLはFOBとHIF-αの分解を介してVHL病を制御する2014

    • Author(s)
      1.奥村 文彦, 植松 桂司, 松崎 真理子, 平野 みえ, 奥村 晶子, 錦見 昭彦, 金森 正和, 執印 太郎, 福井 宣規, 中務 邦雄, 嘉村 巧
    • Organizer
      第37回 日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2014-11-26
    • Related Report
      2014 Annual Research Report
  • [Presentation] Activation of PKR by ubiquitin-like molecule ISG15 modification down-regulates protein translation2013

    • Author(s)
      Fumihiko Okumura
    • Organizer
      The Ubiquitin-Proteasome System: From Basic Mechanisms to Pathophysiological Roles
    • Place of Presentation
      札幌市
    • Related Report
      2013 Research-status Report
  • [Presentation] Regulation of protein translation by ISG15-modified PKR2013

    • Author(s)
      奥村 文彦,奥村 晶子,植松 桂司,畠山 鎮次,Dong-er Zhang,嘉村 巧
    • Organizer
      日本分子生物学会年会
    • Place of Presentation
      神戸市
    • Related Report
      2013 Research-status Report

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Published: 2014-07-25   Modified: 2019-07-29  

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