Global expression profiling of yeast treated with an inhibitor of amino acid biosynthesis, sulfometuron methyl

被引:99
作者
Jia, MH
Larossa, RA
Lee, JM
Rafalski, A
Derose, E
Gonye, G
Xue, ZX
机构
[1] DuPont Co Inc, Cent Res, Expt Stn, Wilmington, DE 19880 USA
[2] DuPont Agr Biotechnol, Wilmington, DE 19880 USA
关键词
DNA microarray; sulfometuron methyl; metabolic regulation;
D O I
10.1152/physiolgenomics.2000.3.2.83
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The expression pattern of 1,529 yeast genes in response to sulfometuron methyl (SM) was analyzed by DNA microarray technology. SM, a potent herbicide, inhibits acetolactate synthase, a branched-chain amino acid biosynthetic enzyme. Exposure of yeast cells to 0.2 mu g/ml SM resulted in 40% growth inhibition, a Gcn4p-mediated induction of genes involved in amino acid and cofactor biosynthesis, and starvation response. The accumulation of intermediates led to the induction of stress response genes and the repression of genes involved in carbohydrate metabolism, nucleotide biosynthesis, and sulfur assimilation. Extended exposure to SM led to a relaxation of the initial response and induction of sugar transporter and ergosterol biosynthetic genes, as well as repression of histone and lipid metabolic genes. Exposure to 5 mu g/ml SM resulted in >98% growth inhibition and stimulated a similar initial expression change, but with no relaxation after extended exposure. Instead, more stress response and DNA damage repair genes become induced, suggesting a serious cellular consequence. Other salient features of metabolic regulation, such as the coordinated expression of cofactor biosynthetic genes with amino acid biosynthetic ones, were evident from our data. A potential link between SM sensitivity and ergosterol metabolism was uncovered by expression profiling and confirmed by genetic analysis.
引用
收藏
页码:83 / 92
页数:10
相关论文
共 60 条
[1]   METHOD FOR DETECTION OF SPECIFIC RNAS IN AGAROSE GELS BY TRANSFER TO DIAZOBENZYLOXYMETHYL-PAPER AND HYBRIDIZATION WITH DNA PROBES [J].
ALWINE, JC ;
KEMP, DJ ;
STARK, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5350-5354
[2]  
BENSON PF, 1984, GENETIC BIOCH DISORD, P274
[3]   EXPRESSION OF HETEROLOGOUS GENES IN SACCHAROMYCES-CEREVISIAE FROM VECTORS UTILIZING THE GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GENE PROMOTER [J].
BITTER, GA ;
EGAN, KM .
GENE, 1984, 32 (03) :263-274
[4]  
BOGOSIAN G, 1989, J BIOL CHEM, V264, P531
[5]   Genetics - Yeast as a model organism [J].
Botstein, D ;
Chervitz, SA ;
Cherry, JM .
SCIENCE, 1997, 277 (5330) :1259-1260
[6]   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
[7]   Comparison of the complete protein sets of worm and yeast: Orthology and divergence [J].
Chervitz, SA ;
Aravind, L ;
Sherlock, G ;
Ball, CA ;
Koonin, EV ;
Dwight, SS ;
Harris, MA ;
Dolinski, K ;
Mohr, S ;
Smith, T ;
Weng, S ;
Cherry, JM ;
Botstein, D .
SCIENCE, 1998, 282 (5396) :2022-2028
[8]   COREGULATION OF PURINE AND HISTIDINE BIOSYNTHESIS BY THE TRANSCRIPTIONAL ACTIVATORS BAS1 AND BAS2 [J].
DAIGNANFORNIER, B ;
FINK, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (15) :6746-6750
[9]   Role of the Myb-like protein Bas1p in Saccharomyces cerevisiae:: a proteome analysis [J].
Denis, V ;
Boucherie, H ;
Monribot, C ;
Daignan-Fornier, B .
MOLECULAR MICROBIOLOGY, 1998, 30 (03) :557-566
[10]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686