Dimethyl sulfoxide exposure facilitates phospholipid biosynthesis and cellular membrane proliferation in yeast cells

被引:68
作者
Murata, Y
Watanabe, T
Sato, M
Momose, Y
Nakahara, T
Oka, S
Iwahashi, H
机构
[1] Natl Inst Adv Ind Sci Technol, Int Patent Organism Depositary, Tsukuba, Ibaraki 3058566, Japan
[2] Natl Inst Adv Ind Sci Technol, Res Inst Biol Resources, Tsukuba, Ibaraki 3058566, Japan
关键词
D O I
10.1074/jbc.M300450200
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
Me2SO is a polar solvent that is widely used in biochemistry, pharmacology, and industry. Although there are several reports in the literature concerning the biological effects of Me2SO, the total cellular response remains unclear. In this paper, DNA microarray technology combined with the hierarchical clustering bioinformatics tool was used to assess the effects of Me2SO on yeast cells. We found that yeast exposed to Me2SO increased phospholipid biosynthesis through up-regulated gene expression. It was confirmed by Northern blotting that the level of INO1 and OPI3 gene transcripts, encoding key enzymes in phospholipid biosynthesis, were significantly elevated following treatment with Me2SO. Furthermore, the phospholipid content of the cells increased during exposure to Me2SO as shown by conspicuous incorporation of a lipophilic fluorescent dye (3,3'-dihexyloxacarbocyanine iodide) into the cell membranes. From these results we propose that Me2SO treatment induces membrane proliferation in yeast cells to alleviate the adverse affects of this chemical on membrane integrity.
引用
收藏
页码:33185 / 33193
页数:9
相关论文
共 51 条
[1]  
Ausubel FM., 1994, Curr. Protoc. Mol. Biol
[2]   DIMETHYL-SULFOXIDE REDUCTASE-ACTIVITY BY ANAEROBICALLY GROWN ESCHERICHIA-COLI HB101 [J].
BILOUS, PT ;
WEINER, JH .
JOURNAL OF BACTERIOLOGY, 1985, 162 (03) :1151-1155
[3]   MANIPULATION OF MYOGENESIS INVITRO - REVERSIBLE INHIBITION BY DMSO [J].
BLAU, HM ;
EPSTEIN, CJ .
CELL, 1979, 17 (01) :95-108
[4]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[5]   IN02, a positive regulator of lipid biosynthesis, is essential for the formation of inducible membranes in yeast [J].
Block-Alper, L ;
Webster, P ;
Zhou, XH ;
Supeková, L ;
Wong, WH ;
Schultz, PG ;
Meyer, DI .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (01) :40-51
[6]   Dimethyl sulfoxide affects the selection of splice sites [J].
Bolduc, L ;
Labrecque, B ;
Cordeau, M ;
Blanchette, M ;
Chabot, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) :17597-17602
[7]   Variations in mRNA transcript levels of cell wall-associated genes of Saccharomyces cerevisiae following spheroplasting [J].
Braley, R ;
Chaffin, WL .
FEMS MICROBIOLOGY LETTERS, 1999, 181 (01) :177-185
[8]   New potential cell wall glucanases of Saccharomyces cerevisiae and their involvement in mating [J].
Cappellaro, C ;
Mrsa, V ;
Tanner, W .
JOURNAL OF BACTERIOLOGY, 1998, 180 (19) :5030-5037
[9]  
CARMAN GM, 1989, ANNU REV BIOCHEM, V58, P635, DOI 10.1146/annurev.biochem.58.1.635
[10]   Regulation of phospholipid biosynthesis in the yeast Saccharomyces cerevisiae [J].
Carman, GM ;
Zeimetz, GM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (23) :13293-13296