Genome-wide studies on the nuclear PDR3-controlled response to mitochondrial dysfunction in yeast

被引:68
作者
Devaux, F
Carvajal, E
Moye-Rowley, S
Jacq, C
机构
[1] Ecole Normale Super, CNRS, UMR 8541, Lab Genet Mol, F-75230 Paris 05, France
[2] Univ Estado Rio De Janeiro, Dept Biol Celular & Genet, BR-20550013 Rio De Janeiro, Brazil
[3] Univ Iowa, Dept Physiol & Biophys, Iowa City, IA 52242 USA
关键词
yeast; microarray; drug resistance; mitochondrion;
D O I
10.1016/S0014-5793(02)02387-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gain-of-function mutations in the transcription factors Pdr1p and Pdr3p lead to the up-regulation of genes controlling plasma membrane properties. Pdr3p is involved in a retrograde response in which mitochondrial dysfunctions activate PDR5, a gene encoding an ABC membrane transporter. We carried out genome-wide analyses of the PDR3-controlled genes activated by the deletion of the mitochondrial DNA. We present evidence showing that PDR1 does not interfere with this PDR3 response. We also showed that the mitochondrially activated PDR3 response is highly sensitive to both yeast strain variations and carbon sources. These observations explain the apparent discrepancies in published studies and better describe the connections between the mitochondrial state and plasma membrane properties. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:25 / 28
页数:4
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