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Study on regulation of addipocyte differentiation through the control of mRNA splicing activity

Research Project

Project/Area Number 26670134
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field General medical chemistry
Research InstitutionUniversity of Toyama

Principal Investigator

Kaida Daisuke  富山大学, 先端ライフサイエンス拠点, 准教授 (60415122)

Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsスプライシング / snRNP
Outline of Final Research Achievements

We treated mouse 3T3-L1 cells with a splicing inhibitor that binds and inhibits U2 snRNP, and found that adipogenesis was inhibited in a dose dependent manner. The significant inhibition of adipogenesis was observed if the cells were treated with the splicing inhibitor when the cells were cultured in differentiation medium.
We also found that some introns showed resistance against splicing inhibition in a intron- and snRNA-dependent manner. These dependency might affect differentiation efficiency.

Report

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

    (1 results)

All 2016

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results)

  • [Journal Article] The reciprocal regulation between splicing and 3′‐end processing2016

    • Author(s)
      Daisuke Kaida
    • Journal Title

      Wiley Interdisciplinary Reviews: RNA

      Volume: 7 Issue: 4 Pages: 499-511

    • DOI

      10.1002/wrna.1348

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant

URL: 

Published: 2014-04-04   Modified: 2017-05-10  

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