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Formation and organization of ER exit site

Research Project

Project/Area Number 26840031
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Functional biochemistry
Research InstitutionThe University of Tokyo

Principal Investigator

YORIMITSU Tomohiro  東京大学, 大学院総合文化研究科, 助教 (00534364)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywords小胞体 / 輸送小胞 / COPII / GTPaes / 輸送 / GTPase / GTP加水分解 / Sar1 / Sec16 / COPII小胞 / ER exit sites
Outline of Final Research Achievements

COPII-coated vesicle carriers, which mediate transport of cargo molecules from the ER to the Golgi complex, are formed at specific domains of the ER membranes, called ER exit sites (ERESs). Regulation of Sar1 GTPase activity is an important process for COPII vesicle formation. Sec16 is essential for ER-Golgi transport and suggested to play a crucial role in ERES formation. Here I investigated Sec16 function and shed light on new mechanistic insights. I find that the N-terminal region of Sec16 can activates Sar1 GTPase. The domain for GTPase activation is identified in the N-terminal region and found to be required for Sec16 function in membrane association and ERES formation. Moreover, I report that the N-terminal region is able to facilitate COPII-mediated vesicle formation. These results provide novel regulatory mechanisms of how Sec16 organizes ERES and potentiates COPII action for vesicle formation.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (6 results)

All 2016 2015 2014

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Open Access: 1 results) Presentation (4 results) (of which Invited: 1 results)

  • [Journal Article] Distribution of Sec24 isoforms to each ER exit site is dynamically regulated in Saccharomyces cerevisiae2015

    • Author(s)
      Iwasaki, H., Yorimitsu, T., Sato, K.
    • Journal Title

      FEBS Letters

      Volume: 589 Issue: 11 Pages: 1234-1239

    • DOI

      10.1016/j.febslet.2015.04.006

    • Related Report
      2015 Research-status Report
    • Peer Reviewed
  • [Journal Article] Molecular mechanisms of Sar/Arf GTPases in vesicular trafficking in yeast and plants.2014

    • Author(s)
      Yorimitsu, T., Sato, K., Takeuchi, M.
    • Journal Title

      Front. Plant Sci.

      Volume: 5 Pages: 411-411

    • DOI

      10.3389/fpls.2014.00411

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] COPII小胞カーゴのER exit sitesへの集積とSec16機能の関連性2016

    • Author(s)
      依光朋宏、佐藤健
    • Organizer
      第89回日本生化学会大会
    • Place of Presentation
      仙台国際センター(宮城県仙台市)
    • Year and Date
      2016-09-26
    • Related Report
      2016 Annual Research Report
  • [Presentation] Sec16 N末端領域によるCOPIIタンパク質の制御とCOPII小胞の形成機構2015

    • Author(s)
      依光朋宏、佐藤 健
    • Organizer
      BMB2015
    • Place of Presentation
      神戸ポートアイランド (兵庫県神戸市)
    • Year and Date
      2015-12-01
    • Related Report
      2015 Research-status Report
  • [Presentation] 小胞体におけるCOPII小胞形成部位ER Exit sitesの機能と制御2015

    • Author(s)
      依光朋宏、佐藤 健
    • Organizer
      第67回日本細胞生物学会大会
    • Place of Presentation
      タワーホール船堀 (東京都江戸川区)
    • Year and Date
      2015-06-30
    • Related Report
      2015 Research-status Report
    • Invited
  • [Presentation] COPII小胞形成におけるSec16 N末端領域の機能解析2014

    • Author(s)
      依光朋宏、佐藤 健
    • Organizer
      第87回日本生化学会大会
    • Place of Presentation
      国立京都国際会館 (京都府京都市)
    • Year and Date
      2014-10-16
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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