Old yellow enzyme interferes with Bax-induced NADPH loss and lipid peroxidation in yeast

被引:16
作者
Reekmans, R
De Smet, K
Chen, CY
Van Hummelen, P
Contreras, R
机构
[1] State Univ Ghent VIB, Dept Mol Biomed Res, Unit Fundamental & Appl Biol, B-9052 Zwijnaarde, Belgium
[2] VIB, Microarry Facil, B-3000 Louvain, Belgium
关键词
old yellow enzyme; Bax; cell death; oxidative stress; NADPH decrease; lipid peroxidation;
D O I
10.1016/j.femsyr.2004.12.010
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The yeast transcriptional response to murine Bax expression was compared with the changes induced by H2O2 treatment via microarray technology. Although most of the Bax-responsive genes were also triggered by H2O2 treatment, OYE3, ICY2, MLS1 and BTN2 were validated to have a Bax-specific transcriptional response not shared with the oxidative stress trigger. In knockout experiments, only deletion of OYE3, coding for yeast Old yellow enzyme, attenuated the rate of Bax-induced growth arrest, cell death and NADPH decrease. Lipid peroxidation was completely absent in Delta OYE3 expressing Bax. However, the absence of OYE3 sensitized yeast cells to H2O2-induced cell death, and increased the rate of NADPH decrease and lipid peroxidation. Our results clearly indicate that OYE3 interferes with Bax- and H2O2-induced lipid peroxidation and cell death in Saccharomyces cerevisiae. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:711 / 725
页数:15
相关论文
共 100 条
[1]   A trace amount of the human pro-apoptotic factor bax induces bacterial death accompanied by damage of DNA [J].
Asoh, S ;
Nishimaki, K ;
Nanbu-Wakao, R ;
Ohta, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (18) :11384-11391
[2]   Aspirin commits yeast cells to apoptosis depending on carbon source [J].
Balzan, R ;
Sapienza, K ;
Galea, DR ;
Vassallo, N ;
Frey, H ;
Bannister, WH .
MICROBIOLOGY-SGM, 2004, 150 :109-115
[3]   Bax, but not Bcl-xL, decreases the lifetime of planar phospholipid bilayer membranes at subnanomolar concentrations [J].
Basañez, G ;
Nechushtan, A ;
Drozhinin, O ;
Chanturiya, A ;
Choe, E ;
Tutt, S ;
Wood, KA ;
Hsu, YT ;
Zimmerberg, J ;
Youle, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5492-5497
[4]   Yeast mutants resistant to Bax lethality reveal distinct vacuolar and mitochondrial alterations [J].
Belhocine, S ;
Mbithe, C ;
Dimitrova, I ;
Kampranis, SC ;
Makris, AM .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (08) :946-948
[5]   The product of the UTH1 gene, required for Bax-induced cell death in yeast, is involved in the response to rapamycin [J].
Camougrand, N ;
Grelaud-Coq, A ;
Marza, E ;
Priault, M ;
Bessoule, JJ ;
Manon, S .
MOLECULAR MICROBIOLOGY, 2003, 47 (02) :495-506
[6]   Remodeling of yeast genome expression in response to environmental changes [J].
Causton, HC ;
Ren, B ;
Koh, SS ;
Harbison, CT ;
Kanin, E ;
Jennings, EG ;
Lee, TI ;
True, HL ;
Lander, ES ;
Young, RA .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (02) :323-337
[7]   Evolutionarily conserved cytoprotection provided by Bax Inhibitor-1 homologs from animals, plants, and yeast [J].
Chae, HJ ;
Ke, N ;
Kim, HR ;
Chen, SR ;
Godzik, A ;
Dickman, M ;
Reed, JC .
GENE, 2003, 323 :101-113
[8]   Tomato phospholipid hydroperoxide glutathione peroxidase inhibits cell death induced by Bax and oxidative stresses in yeast and plants [J].
Chen, SR ;
Vaghchhipawala, Z ;
Li, W ;
Asard, H ;
Dickman, MB .
PLANT PHYSIOLOGY, 2004, 135 (03) :1630-1641
[9]   Discrimination between paralogs using microarray analysis: Application to the Yap1p and Yap2p transcriptional networks [J].
Cohen, BA ;
Pilpel, Y ;
Mitra, RD ;
Church, GM .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (05) :1608-1614
[10]   Induction of apoptosis in yeast and mammalian cells by exposure to 1,10-phenanthroline metal complexes [J].
Coyle, B ;
Kinsella, P ;
McCann, M ;
Devereux, M ;
O'Connor, R ;
Clynes, M ;
Kavanagh, K .
TOXICOLOGY IN VITRO, 2004, 18 (01) :63-70