The H2O2 stimulon in Saccharomyces cerevisiae

被引:475
作者
Godon, C
Lagniel, G
Lee, J
Buhler, JM
Kieffer, S
Perrot, R
Boucherie, H
Toledano, MB
Labarre, J
机构
[1] CEA Saclay, Serv Biochim & Genet Mol, F-91191 Gif Sur Yvette, France
[2] Rutgers State Univ, Coll Pharm, Dept Pharmacol & Toxicol, Piscataway, NJ 08855 USA
[3] CNRS, Inst Biochim & Genet Cellulaires, UPR 9026, F-33077 Bordeaux, France
[4] CEA, Dept Biol Mol & Struct, F-38054 Grenoble 09, France
关键词
D O I
10.1074/jbc.273.35.22480
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
The changes in gene expression underlying the yeast adaptive stress response to H2O2 were analyzed by comparative two-dimensional gel electrophoresis of total cell proteins. The synthesis of at least 115 proteins is stimulated by H2O2, whereas 52 other proteins are repressed by this treatment. We have identified 71 of the stimulated and 44 of the repressed targets. The kinetics and dose-response parameters of the H2O2, genomic response were also analyzed. Identification of these proteins and their mapping into specific cellular processes give a distinct picture of the way in which yeast cells adapt to oxidative stress. As expected, H2O2-responsive targets include an important number of heat shock proteins and proteins with reactive oxygen intermediate scavenging activities. Exposure to H2O2 also results in a slowdown of protein biosynthetic processes and a stimulation of protein degradation pathways. Finally, the most remarkable result inferred from this study is the resetting of carbohydrate metabolism minutes after the exposure to H2O2. Carbohydrate fluxes are redirected to the regeneration of NADPH at the expense of glycolysis. This study represents the first genome-wide characterization of a H2O2-inducible stimulon in a eukaryote.
引用
收藏
页码:22480 / 22489
页数:10
相关论文
共 60 条
[1]  
Ahn SM, 1996, BIOCHEM MOL BIOL INT, V39, P1007
[2]   ARABIDOPSIS-THALIANA NADPH OXIDOREDUCTASE HOMOLOGS CONFER TOLERANCE OF YEASTS TOWARD THE THIOL-OXIDIZING DRUG DIAMIDE [J].
BABIYCHUK, E ;
KUSHNIR, S ;
BELLESBOIX, E ;
VANMONTAGU, M ;
INZE, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) :26224-26231
[3]   HIGH CONTROL COEFFICIENT OF TRANSKETOLASE IN THE NONOXIDATIVE PENTOSE-PHOSPHATE PATHWAY OF HUMAN ERYTHROCYTES - NMR, ANTIBODY, AND COMPUTER-SIMULATION STUDIES [J].
BERTHON, HA ;
KUCHEL, PW ;
NIXON, PF .
BIOCHEMISTRY, 1992, 31 (51) :12792-12798
[4]   Two-dimensional gel protein database of Saccharomyces cerevisiae [J].
Boucherie, H ;
Sagliocco, F ;
Joubert, R ;
Maillet, I ;
Labarre, J ;
Perrot, M .
ELECTROPHORESIS, 1996, 17 (11) :1683-1699
[5]  
CHAE HZ, 1994, J BIOL CHEM, V269, P27670
[6]  
CHAE HZ, 1994, BIOFACTORS, V4, P177
[7]   The ubiquitin-mediated proteolytic system: Involvement of molecular chaperones, degradation of oncoproteins, and activation of transcriptional regulators [J].
Ciechanover, A ;
Laszlo, A ;
Bercovich, B ;
Stancovski, I ;
Alkalay, I ;
Ben-Neriah, Y ;
Orian, A .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1995, 60 :491-501
[8]   INDUCIBILITY OF THE RESPONSE OF YEAST-CELLS TO PEROXIDE STRESS [J].
COLLINSON, LP ;
DAWES, IW .
JOURNAL OF GENERAL MICROBIOLOGY, 1992, 138 :329-335
[9]   HEAT-SHOCK PROTEINS - MOLECULAR CHAPERONES OF PROTEIN BIOGENESIS [J].
CRAIG, EA ;
GAMBILL, BD ;
NELSON, RJ .
MICROBIOLOGICAL REVIEWS, 1993, 57 (02) :402-414
[10]   ADAPTIVE RESPONSE AND OXIDATIVE STRESS [J].
CRAWFORD, DR ;
DAVIES, KJA .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :25-28