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Regulation of Mphase progression by the SCFCdc4 ubiquitin ligase.

Research Project

Project/Area Number 23570001
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Genetics/Genome dynamics
Research InstitutionNihon University

Principal Investigator

KISHI Tsutomu  日本大学, 工学部, 准教授 (80260024)

Project Period (FY) 2011 – 2013
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywordsゲノム構築・再編・維持 / 細胞周期 / 染色体分離 / ユビキチンリガーゼ / 転写 / M期終了 / 転写制御 / サイクリン / フィードバック阻害
Outline of Final Research Achievements

Swi5 is a transcription factor that activates transcription of genes required for G1 functions in yeast. We previously showed that Swi5 is degraded by the SCFCdc4 ubiquitin ligase. In this study, we constructed a stabilized Swi5 by modifying residues required for the SCFCdc4-dependent degradation. We found that onset of S-phase, chrosomome segregation, and M-phase exit are inhibited in cells expressing the stabilized Swi5. We found a novel regulatory mechanism of cell cycle: Swi5 induces expression of Sic1 that inhibits initiation of S phase and chromosome segregation, and of Amn1 that inhibits M-phase exit; and degradation of Swi5 by the SCFCdc4 ubiquitin ligase allows proper progression into cell cycle.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (1 results)

All 2011

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

  • [Journal Article] Non-SCF-type F-box protein Roy1/Ymr258c interacts with a Rab5-like GTPase Ypt52 and inhibits Ypt52 function.2011

    • Author(s)
      Liu Y, Nakatsukasa K, Kotera M, Kanada A, Nishimura T, Kishi T, Mimura S, Kamura T.
    • Journal Title

      Mol Biol Cell

      Volume: 28 Pages: 1575-1584

    • Related Report
      2011 Research-status Report
    • Peer Reviewed

URL: 

Published: 2011-08-05   Modified: 2019-07-29  

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