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On the Regulation of Membrane Biogenesis by Using Yeast Model Systems

Research Project

Project/Area Number 05044123
Research Category

Grant-in-Aid for international Scientific Research

Allocation TypeSingle-year Grants
SectionJoint Research
Research InstitutionFaculty of Agriculture, The University of Tokyo

Principal Investigator

TAKAGI Masamichi  Faculty of Agriculture, The University of Tokyo, Professor, 農学部, 教授 (50018339)

Co-Investigator(Kenkyū-buntansha) SCHUNCK Wolf-Hagen  Max-Delbruck-Centre for Molecular Medicine, Head of gr
OHTA Akinori  Faculty of Agriculture, The University of Tokyo, 農学部, 助教授 (30125885)
Project Period (FY) 1993
Project Status Completed (Fiscal Year 1993)
Budget Amount *help
¥2,500,000 (Direct Cost: ¥2,500,000)
Fiscal Year 1993: ¥2,500,000 (Direct Cost: ¥2,500,000)
Keywordsyeast / Candida maltosa / ER membrane / cytochrome P450 / expression vector / Immuno-electron microscopy
Research Abstract

We have a working hypothesis on the ER membrane biogenesis ; that is, when one of many protein components of the ER membrane is produced in a large amount, the protein is incorporated into the ER membrane to disturb it in some way, then unknown signals are produced from the membrane, which induce synthesis of various components of the membrane. Our idea is that this is one of the mechanisms to proliferate cellular membrane in general by stimuli from outside the cells.
To prove this, we constructed an expression vector for a yeast, Candida maltosa, which is known to proliferate the ER membrane under some specific culture conditions. By using this expression vector, we have induced cytochrome P450, one of the major ER membrane protein components of this yeast and examined proliferation of the ER membrane by immuno-electron microscopy. We have found that the result of this experiment support our working idea on the ER membrane proliferation as described above.

Report

(1 results)
  • 1993 Final Research Report Summary

URL: 

Published: 1993-04-01   Modified: 2016-04-21  

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