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2013 Fiscal Year Final Research Report

Quality control system that monitors ribosomes damaged by verotoxin

Research Project

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Project/Area Number 24657117
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Molecular biology
Research InstitutionKyoto University

Principal Investigator

KITABATAKE Makoto  京都大学, ウイルス研究所, 助教 (10321754)

Project Period (FY) 2012-04-01 – 2014-03-31
Keywordsリボソーム
Research Abstract

Verotoxin is produced by enterohemorrhagic E. coli. It targets a small domain called SRL (Sarcin-Ricin Loop) in the host ribosomal RNA. The target site of this toxin was precisely determined; however, the consequence of this damage, including the effect on the ribosomal function and the cellular stress-response systems, has not been explored extensively. In this research, we tackled this problem using S. cerevisiae system as a model. We revealed that 25S rRNA with a mutation in SRL is nonfunctional and selectively degraded in vivo. From 5000 mutant strains of the yeast knock-out collection, we identified several strains that accumulate the SRL mutant 25S rRNA. Interestingly, the genes involved in the degradation of the SRL mutant are partially overlapped with those involved in 25S NRD (degradation pathway for another type of nonfunctional 25S rRNA). These results suggest a general quality control mechanism that monitors a wealth of defects caused by a number of reasons.

  • Research Products

    (2 results)

All 2014 2013

All Presentation (2 results)

  • [Presentation] 真核生物リボソームの品質管理2014

    • Author(s)
      北畠真
    • Organizer
      国立遺伝学研究所研究会「単細胞システムの細胞構築・運動・増殖機構の研究」
    • Place of Presentation
      国立遺伝学研究所講堂
    • Year and Date
      2014-03-25
  • [Presentation] 真核生物リボソームRNAの機能を検査し,不良品を分解する共通のメカニズム2013

    • Author(s)
      北畠真
    • Organizer
      日本分子生物学会年会
    • Place of Presentation
      神戸
    • Year and Date
      2013-12-04

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Published: 2015-06-25  

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