Anaerobicity prepares Saccharomyces cerevisiae cells for faster adaptation to osmotic shock

被引:44
作者
Krantz, M
Nordlander, B
Valadi, H
Johansson, M
Gustafsson, L
Hohmann, S
机构
[1] Univ Gothenburg, Dept Cell & Mol Biol Microbiol, S-40530 Gothenburg, Sweden
[2] Chalmers Univ Technol, Dept Chem & Biosci Mol Biotechnol, S-41296 Gothenburg, Sweden
[3] Chalmers Univ Technol, Dept Chem Engn & Environm Sci Chem React Engn, S-41296 Gothenburg, Sweden
关键词
D O I
10.1128/EC.3.6.1381-1390.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Yeast cells adapt to hyperosmotic shock by accumulating glycerol and altering expression of hundreds of genes. This transcriptional response of Saccharomyces cerevisiae to osmotic shock encompasses genes whose products are implicated in protection from oxidative damage. We addressed the question of whether osmotic shock caused oxidative stress. Osmotic shock did not result in the generation of detectable levels of reactive oxygen species (ROS). To preclude any generation of ROS, osmotic shock treatments were performed in anaerobic cultures. Global gene expression response profiles were compared by employing a novel two-dimensional cluster analysis. The transcriptional profiles following osmotic shock under anaerobic and aerobic conditions were qualitatively very similar. In particular, it appeared that expression of the oxidative stress genes was stimulated upon osmotic shock even if there was no apparent need for their function. Interestingly, cells adapted to osmotic shock much more rapidly under anaerobiosis, and the signaling as well as the transcriptional response was clearly attenuated under these conditions. This more rapid adaptation is due to an enhanced glycerol production capacity in anaerobic cells, which is caused by the need for glycerol production in redox balancing. Artificially enhanced glycerol production led to an attenuated response even under aerobic conditions. These observations demonstrate the crucial role of glycerol accumulation and turgor recovery in determining the period of osmotic shock-induced signaling and the profile of cellular adaptation to osmotic shock.
引用
收藏
页码:1381 / 1390
页数:10
相关论文
共 41 条
[1]   GPD1, WHICH ENCODES GLYCEROL-3-PHOSPHATE DEHYDROGENASE, IS ESSENTIAL FOR GROWTH UNDER OSMOTIC-STRESS IN SACCHAROMYCES-CEREVISIAE, AND ITS EXPRESSION IS REGULATED BY THE HIGH-OSMOLARITY GLYCEROL RESPONSE PATHWAY [J].
ALBERTYN, J ;
HOHMANN, S ;
THEVELEIN, JM ;
PRIOR, BA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (06) :4135-4144
[2]   Characterization of an upstream activation sequence and two Rox1p-responsive sites controlling the induction of the yeast HEM13 gene by oxygen and heme deficiency [J].
Amillet, JM ;
Buisson, N ;
LabbeBois, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (40) :24425-24432
[3]  
[Anonymous], [No title captured]
[4]   The two isoenzymes for yeast NAD(+)-dependent glycerol 3-phosphate dehydrogenase encoded by GPD1 and GPD2 have distinct roles in osmoadaptation and redox regulation [J].
Ansell, R ;
Granath, K ;
Hohmann, S ;
Thevelein, JM ;
Adler, L .
EMBO JOURNAL, 1997, 16 (09) :2179-2187
[5]   Rck1 and Rck2 MAPKAP kinases and the HOG pathway are required for oxidative stress resistance [J].
Bilsland, E ;
Molin, C ;
Swaminathan, S ;
Ramne, A ;
Sunnerhagen, P .
MOLECULAR MICROBIOLOGY, 2004, 53 (06) :1743-1756
[6]  
Bjorkqvist S, 1997, APPL ENVIRON MICROB, V63, P128
[7]   MICROCALORIMETRIC MONITORING OF GROWTH OF SACCHAROMYCES-CEREVISIAE - OSMOTOLERANCE IN RELATION TO PHYSIOLOGICAL-STATE [J].
BLOMBERG, A ;
LARSSON, C ;
GUSTAFSSON, L .
JOURNAL OF BACTERIOLOGY, 1988, 170 (10) :4562-4568
[8]   Msn2p and Msn4p control a large number of genes induced at the diauxic transition which are repressed by cyclic AMP in Saccharomyces cerevisiae [J].
Boy-Marcotte, E ;
Perrot, M ;
Bussereau, F ;
Boucherie, H ;
Jacquet, M .
JOURNAL OF BACTERIOLOGY, 1998, 180 (05) :1044-1052
[9]   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
[10]  
Costenoble R, 2000, YEAST, V16, P1483, DOI 10.1002/1097-0061(200012)16:16<1483::AID-YEA642>3.0.CO