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Analysis of mechanism of resetting replicative life span by imaging aging-associated factors

Research Project

Project/Area Number 15K18531
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Cell biology
Research InstitutionKyushu University

Principal Investigator

Okada Satoshi  九州大学, 医学研究院, 助教 (30734488)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2015: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Keywords出芽酵母 / 細胞老化 / オルガネラ / イメージング / 胞子形成 / 細胞分裂寿命
Outline of Final Research Achievements

Budding yeast strains in which ageing-related organelles are visualized by C-terminal tagging with green or red fluorescent protein were constructed. Live cell imaging conditions for these strains were optimized. To achieve long-term time-lapse live cell imaging, a microfluidics-based stage top cell culture device was introduced on a microscope. On the device, cell culture conditions for high efficiency sporulation induction were optimized. By development of BiFC system of novel bright fluorescent protein, RENT complexes containing an ageing-related factor, Sir2, were successfully visualized in living yeast cells.

Report

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

    (1 results)

All 2017

All Presentation (1 results)

  • [Presentation] 高輝度・高光安定性蛍光タンパク質のBiFC 化とその利用について2017

    • Author(s)
      岡田悟
    • Organizer
      酵母研究若手の会第3回研究会
    • Place of Presentation
      京都大学宇治キャンパス
    • Year and Date
      2017-03-16
    • Related Report
      2016 Annual Research Report

URL: 

Published: 2015-04-16   Modified: 2018-03-22  

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