Severe reduction of superoxide dismutase activity in the yeast Saccharomyces cerevisae with the deletion or overexpression of GTS1

被引:4
作者
Abudugupur, A
Xu, ZJ
Mitsui, K
Hisaki, H
Ueda, N
Amemiya, T
Tsurugi, K
机构
[1] Univ Yamanashi, Fac Med, Dept Biochem 2, Tamaho, Yamanashi 4093898, Japan
[2] Teikyo Univ, Sch Med, Dept Biochem, Tokyo 1730002, Japan
关键词
Saccharomyces cerevisiae; GTS1; superoxide dismutase; copper;
D O I
10.1016/S0378-1097(03)00377-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report herein that the level of reactive oxygen species (ROS) observed using dihydrorhodamine is much higher in either GTS1-deleted (gts1Delta) or GTS1-overexpressing (TMpGTS1) transformants than in the wild-type and that the levels of protein carbonyls are increased and the glutathione levels are decreased in both transformants. Consistently, the activities of superoxide dismutases (SODs) in both gts1Delta and TMpGTS1 were severely weakened, while the protein levels of both Cu/Zn-SOD and Mn-SOD were not so changed. As the intracellular copper levels were significantly increased in both transformants, we hypothesized that, in either gts1Delta or TMpGTS1 cells, the imbalanced homeostasis of copper induced an accumulation of ROS which caused inactivation of SODs further increasing ROS levels. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:141 / 145
页数:5
相关论文
共 26 条
[1]   An ARL1 mutation affected autophagic cell death in yeast, causing a defect in central vacuole formation [J].
Abudugupur, A ;
Mitsui, K ;
Yokota, S ;
Tsurugi, K .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (02) :158-168
[2]   Characterization of the binding interface between the copper chaperone Atx1 and the first cytosolic domain of Ccc2 ATPase [J].
Arnesano, F ;
Banci, L ;
Bertini, I ;
Cantini, F ;
Ciofi-Baffoni, S ;
Huffman, DL ;
O'Halloran, TV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (44) :41365-41376
[3]   Effect of Cu,Zn superoxide dismutase disruption mutation on replicative senescence in Saccharomyces cerevisiae [J].
Barker, MG ;
Brimage, LJE ;
Smart, KA .
FEMS MICROBIOLOGY LETTERS, 1999, 177 (02) :199-204
[4]   THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE [J].
BULL, PC ;
THOMAS, GR ;
ROMMENS, JM ;
FORBES, JR ;
COX, DW .
NATURE GENETICS, 1993, 5 (04) :327-337
[5]   WILSON DISEASE AND MENKES DISEASE - NEW HANDLES ON HEAVY-METAL TRANSPORT [J].
BULL, PC ;
COX, DW .
TRENDS IN GENETICS, 1994, 10 (07) :246-252
[6]   Mitochondrial superoxide dismutase is essential for ethanol tolerance of Saccharomyces cerevisiae in the post-diauxic phase [J].
Costa, V ;
Amorim, MA ;
Reis, E ;
Quintanilha, A ;
MoradasFerreira, P .
MICROBIOLOGY-UK, 1997, 143 :1649-1656
[7]   The copper chaperone for superoxide dismutase [J].
Culotta, VC ;
Klomp, LWJ ;
Strain, J ;
Casareno, RLB ;
Krems, B ;
Gitlin, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (38) :23469-23472
[8]   Protein carbonyl groups as biomarkers of oxidative stress [J].
Dalle-Donne, I ;
Rossi, R ;
Giustarini, D ;
Milzani, A ;
Colombo, R .
CLINICA CHIMICA ACTA, 2003, 329 (1-2) :23-38
[9]   SEQUENCE, MAPPING AND DISRUPTION OF CCC2, A GENE THAT CROSS-COMPLEMENTS THE CA2+-SENSITIVE PHENOTYPE OF CSG1 MUTANTS AND ENCODES A P-TYPE ATPASE BELONGING TO THE CU2+-ATPASE SUBFAMILY [J].
FU, DD ;
BEELER, TJ ;
DUNN, TM .
YEAST, 1995, 11 (03) :283-292
[10]   PRODUCT OF PER LOCUS OF DROSOPHILA SHARES HOMOLOGY WITH PROTEOGLYCANS [J].
JACKSON, FR ;
BARGIELLO, TA ;
YUN, SH ;
YOUNG, MW .
NATURE, 1986, 320 (6058) :185-188