Arsenic induces caspase- and mitochondria-mediated apoptosis in Saccharomyces cerevisiae

被引:42
作者
Du, Li
Yu, Yong
Chen, Jingsi
Liu, Yan
Xia, Yongjing
Chen, Quan
Liu, Xiangjun [1 ]
机构
[1] Tsinghua Univ, Sch Med, Beijing 100084, Peoples R China
[2] Chinese Acad Sci, Inst Zool, Beijing, Peoples R China
关键词
apoptosis; Saccharomyces cerevisiae; arsenic; mitochondria; caspase;
D O I
10.1111/j.1567-1364.2007.00274.x
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
In recent years, it has been shown that yeast, a unicellular organism, undergoes apoptosis in response to various factors. Here we demonstrate that the highly effective anticancer agent arsenic induces apoptotic process in yeast cells. Reactive oxygen species (ROS) production was observed in the process. Moreover, mitochondrial membrane potential decreased after arsenic treatment. Resistance of the rho(0) mutant strain (lacking mtDNA) to arsenic provides further evidence that this death process involves mitochondria. In addition, hypersensitivity of Delta sod1 to arsenic suggests the critical role of ROS. Cell death and DNA fragmentation decreased in a Delta yca1 deletion mutant, indicating the participation of yeast caspase-1 protein in apoptosis. The implications of these findings for arsenic-induced apoptosis are discussed.
引用
收藏
页码:860 / 865
页数:6
相关论文
共 25 条
[1]   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
[2]   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
[3]  
Chen YC, 1998, J CELL PHYSIOL, V177, P324, DOI 10.1002/(SICI)1097-4652(199811)177:2<324::AID-JCP14>3.0.CO
[4]  
2-9
[5]   The S-cerevisiae HtrA-like protein Nma111p is a nuclear serine protease that mediates yeast apoptosis [J].
Fahrenkrog, B ;
Sauder, U ;
Aebi, U .
JOURNAL OF CELL SCIENCE, 2004, 117 (01) :115-126
[6]   Reactive oxygen species regulate activation-induced T cell apoptosis [J].
Hildeman, DA ;
Mitchell, T ;
Teague, TK ;
Henson, P ;
Day, BJ ;
Kappler, J ;
Marrack, PC .
IMMUNITY, 1999, 10 (06) :735-744
[7]   Mitochondrial permeability transition: a common pathway to necrosis and apoptosis [J].
Kim, JS ;
He, LH ;
Lemasters, JJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 304 (03) :463-470
[8]   The cytotoxic action of Bax on yeast cells does not require mitochondrial ADP/ATP carrier but may be related to its import to the mitochondria [J].
Kissová, I ;
Polcic, P ;
Kempná, P ;
Zeman, I ;
Sabová, L ;
Kolarov, J .
FEBS LETTERS, 2000, 471 (01) :113-118
[9]  
Laun P, 2001, MOL MICROBIOL, V39, P1166, DOI 10.1111/j.1365-2958.2001.02317.x
[10]   Assessment of mitochondrial membrane potential in yeast cell populations by flow cytometry [J].
Ludovico, P ;
Sansonetty, F ;
Côrte-Real, M .
MICROBIOLOGY-SGM, 2001, 147 :3335-3343