Functional characterization of human proapoptotic molecules in yeast S-cerevisiae

被引:24
作者
Guscetti, F [1 ]
Nath, N [1 ]
Denko, N [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Radiat Oncol, Div Radiat & Canc Biol, Stanford, CA 94305 USA
关键词
Bcl-2; Bax; Bid; Bad; BNip3; BNip3L; Noxa; Puma; metacaspase;
D O I
10.1096/fj.04-2316fje
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
The presence of a complete (BH1-3) proapoptotic molecule is necessary for the induction of the intrinsic apoptotic cascade in mammalian cells. It is unclear, however, what distinct roles the members of the large family of BH3-only proapoptotic molecules play in apoptosis. Although biochemical analysis of these molecules can characterize binding efficiencies of BH3 family members, the biologic consequences of these interactions are difficult to predict. We have, therefore, established three functional categories of BH3-only human proapoptotic proteins based on their toxicity after expression in budding yeast: directly killing (tBid), sensitizing in Bax/Bcl-2 expressing cells ( Bad or Puma), and non-toxic (BNip3, BNip3L, and Noxa). The mechanism of killing by the proapoptotic molecules in yeast, however, is not due to activation of the recently described yeast metacaspase MCA1.
引用
收藏
页码:464 / +
页数:14
相关论文
共 30 条
[1]  
Bouillet P, 2002, J CELL SCI, V115, P1567
[2]   Expression of the gene encoding the proapoptotic Nip3 protein is induced by hypoxia [J].
Bruick, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :9082-9087
[3]   The product of the UTH1 gene, required for Bax-induced cell death in yeast, is involved in the response to rapamycin [J].
Camougrand, N ;
Grelaud-Coq, A ;
Marza, E ;
Priault, M ;
Bessoule, JJ ;
Manon, S .
MOLECULAR MICROBIOLOGY, 2003, 47 (02) :495-506
[4]  
CHEN JC, 1997, SOFT COMPUT, V1, P19
[5]   The BCL2 family: Regulators of the cellular life-or-death switch [J].
Cory, S ;
Adams, JM .
NATURE REVIEWS CANCER, 2002, 2 (09) :647-656
[6]   BAX and BAK mediate p53-independent suppression of tumorigenesis [J].
Degenhardt, K ;
Chen, GH ;
Lindsten, T ;
White, E .
CANCER CELL, 2002, 2 (03) :193-203
[7]   tBID homooligomerizes in the mitochondrial membrane to induce apoptosis [J].
Grinberg, M ;
Sarig, R ;
Zaltsman, Y ;
Frumkin, D ;
Grammatikakis, N ;
Reuveny, E ;
Gross, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (14) :12237-12245
[8]   Biochemical and genetic analysis of the mitochondrial response of yeast to BAX and BCL-XL [J].
Gross, A ;
Pilcher, K ;
Blachly-Dyson, E ;
Basso, E ;
Jockel, J ;
Bassik, MC ;
Korsmeyer, SJ ;
Forte, M .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (09) :3125-3136
[9]   Role of oxidative phosphorylation in Bax toxicity [J].
Harris, MH ;
Vander Heiden, MG ;
Kron, SJ ;
Thompson, CB .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (10) :3590-3596
[10]   Bcl-2/E1B 19kDa-interacting protein 3-like protein (Bnip3L) interacts with Bcl-2/Bcl-xL and induces apoptosis by altering mitochondrial membrane permeability [J].
Imazu, T ;
Shimizu, S ;
Tagami, S ;
Matsushima, M ;
Nakamura, Y ;
Miki, T ;
Okuyama, A ;
Tsujimoto, Y .
ONCOGENE, 1999, 18 (32) :4523-4529