Caspases in yeast apoptosis-like death:: facts and artefacts

被引:55
作者
Vachova, Libuse
Palkova, Zdena
机构
[1] Charles Univ Prague, Dept Genet & Microbiol, CR-12844 Prague 2, Czech Republic
[2] Acad Sci Czech Republ, Inst Microbiol, Prague, Czech Republic
关键词
caspases and metacaspases; apoptosis and programmed cell death in yeast; yeast multicellular populations; Saccharomyces cerevisiae;
D O I
10.1111/j.1567-1364.2006.00137.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
Various findings suggest that programmed cell death (PCD) is induced in yeast as a response to the impact of a deleterious environment and/or an intracellular defect. Moreover, the specifically localized PCD within multicellular colonies seems to be important for the safe degradation of cell subpopulations to simple compounds that can be used as nutrients by healthy survivors occurring in propitious colony areas, being thus important for proper development and survival of the yeast population. In spite of this, the question remains whether yeast dies by real apoptosis, i.e. death involving caspases, or by other kinds of PCD. A large group of mammalian caspases includes those that are responsible for monitoring of the stimulus and initiating the dying process, as well as those involved in the execution of death. Additionally, paracaspases and metacaspases, that share some homology with real caspases, but possibly differ in substrate specificity, have been identified in plants, fungi, Dictyostelium and metazoa. In yeast, one homologue of caspases, metacaspase Mca1p/Yca1p, has been identified so far, although there are several indications of the presence of other caspase-like activities in yeast. In this minireview, we summarize various data on the possible involvement of Mca1p and other caspase-like activities in yeast PCD.
引用
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页码:12 / 21
页数:10
相关论文
共 41 条
[1]   Involvement of the yeast metacaspase Yca1 in ubp10Δ-programmed cell death [J].
Bettiga, M ;
Calzari, L ;
Orlandi, I ;
Alberghina, L ;
Vai, M .
FEMS YEAST RESEARCH, 2004, 5 (02) :141-147
[2]  
Beynon R.J., 1989, PROTEOLYTIC ENZYMES, P231
[3]   A decade of caspases [J].
Degterev, A ;
Boyce, M ;
Yuan, JY .
ONCOGENE, 2003, 22 (53) :8543-8567
[4]   Structure and zymogen activation of caspases [J].
Donepudi, M ;
Grütter, MG .
BIOPHYSICAL CHEMISTRY, 2002, 101 :145-153
[5]   Caspase inhibitors [J].
Ekert, PG ;
Silke, J ;
Vaux, DL .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (11) :1081-1086
[6]   Inhibition of apoptosis and clonogenic survival of cells expressing crmA variants: optimal caspase substrates are not necessarily optimal inhibitors [J].
Ekert, PG ;
Silke, J ;
Vaux, DL .
EMBO JOURNAL, 1999, 18 (02) :330-338
[7]   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
[8]   Mitochondrial fission proteins regulate programmed cell death in yeast [J].
Fannjiang, Y ;
Cheng, WC ;
Lee, SJ ;
Qi, B ;
Pevsner, J ;
McCaffery, JM ;
Hill, RB ;
Basañez, G ;
Hardwick, JM .
GENES & DEVELOPMENT, 2004, 18 (22) :2785-2797
[9]   Apoptosis in yeast -: a monocellular organism exhibits altruistic behaviour [J].
Fröhlich, KU ;
Madeo, F .
FEBS LETTERS, 2000, 473 (01) :6-9
[10]   Functional characterization of human proapoptotic molecules in yeast S-cerevisiae [J].
Guscetti, F ;
Nath, N ;
Denko, N .
FASEB JOURNAL, 2005, 19 (01) :464-+