Mitochondrial apoptotic pathways induced by Drosophila programmed cell death regulators

被引:8
作者
Clavería, C [1 ]
Torres, M [1 ]
机构
[1] UAM, Dept Immunol & Oncol, Ctr Nacl Biotecnol, CSIC, E-28049 Madrid, Spain
关键词
reaper; grim; hid; sickle; GH3;
D O I
10.1016/S0006-291X(03)00626-0
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
Multicellular organisms eliminate unwanted or damaged cells by cell death, a process essential to the maintenance of tissue homeostasis. Cell death is a tightly regulated event, whose alteration by excess or defect is involved in the pathogenesis of many diseases such as cancer, autoimmune syndromes, and neurodegenerative processes. Studies in model organisms, especially in the nematode Caenorhabditis elegans, have been crucial in identifying the key molecules implicated in the regulation and execution of programmed cell death. In contrast, the study of cell death in Drosophila melanogaster, often an excellent model organism, has identified regulators and mechanisms not obviously conserved in other metazoans. Recent molecular and cellular analyses suggest, however, that the mechanisms of action of the main programmed cell death regulators in Drosophila include a canonical mitochondrial pathway. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:531 / 537
页数:7
相关论文
共 66 条
[1]  
ABRAMS JM, 1993, DEVELOPMENT, V117, P29
[2]   Ectopic E2F expression induces S phase and apoptosis in Drosophila imaginal discs [J].
Asano, M ;
Nevins, JR ;
Wharton, RP .
GENES & DEVELOPMENT, 1996, 10 (11) :1422-1432
[3]   The Drosophila gene hid is a direct molecular target of Ras-dependent survival signaling [J].
Bergmann, A ;
Agapite, J ;
McCall, K ;
Steller, H .
CELL, 1998, 95 (03) :331-341
[4]   Drosophila p53 binds a damage response element at the reaper locus [J].
Brodsky, MH ;
Nordstrom, W ;
Tsang, G ;
Kwan, E ;
Rubin, GM ;
Abrams, JM .
CELL, 2000, 101 (01) :103-113
[5]   DNA-DAMAGE RESPONSES - P53 INDUCTION, CELL-CYCLE PERTURBATIONS, AND APOPTOSIS [J].
CANMAN, CE ;
CHEN, CY ;
LEE, MH ;
KASTAN, MB .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1994, 59 :277-286
[6]   Apoptotic activity of REAPER is distinct from signaling by the tumor necrosis factor receptor 1 death domain [J].
Chen, P ;
Lee, P ;
Otto, L ;
Abrams, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :25735-25737
[7]   grim, a novel cell death gene in Drosophila [J].
Chen, P ;
Nordstrom, W ;
Gish, B ;
Abrams, JM .
GENES & DEVELOPMENT, 1996, 10 (14) :1773-1782
[8]   The damage-responsive Drosophila gene sickle encodes a novel IAP binding protein similar to but distinct from reaper, grim, and hid [J].
Christich, A ;
Kauppila, S ;
Chen, P ;
Sogame, N ;
Ho, SI ;
Abrams, JM .
CURRENT BIOLOGY, 2002, 12 (02) :137-140
[9]  
Clarke PGH, 1996, ANAT EMBRYOL, V193, P81
[10]   GH3, a novel proapoptotic domain in Drosophila Grim, promotes a mitochondrial death pathway [J].
Clavería, C ;
Caminero, E ;
Martínez, C ;
Campuzano, S ;
Torres, M .
EMBO JOURNAL, 2002, 21 (13) :3327-3336