Role of programmed cell death in development

被引:35
作者
Ranganath, RM [1 ]
Nagashree, NR [1 ]
机构
[1] Bangalore Univ, Dept Bot, Cytogenet & Dev Biol Lab, Bangalore 560056, Karnataka, India
来源
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL. 202 | 2001年 / 202卷
关键词
apoptosis; programmed cell death; embryonic development;
D O I
10.1016/S0074-7696(01)02005-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Programmed cell death (PCD) is an integral part of both animal and plant development. In animals, model systems such as Caenorhabditis elegans, Drosophila melanogaster, and mice have shown a general cell death profile of induction, caspase mediation, cell death, and phagocytosis. Tremendous strides have been made in cell death research in animals in the past decade. The ordering of the C. elegans genes Ced-3, 4 and 9, identification of caspase-activated DNase that degrades nuclear DNA during PCD, identification of signal transduction modules involving caspases as well as the caspase-independent pathway, and the involvement of mitochondria are some of the findings of immense value in understanding animal PCDs. Similarly, the caspase inactivation mechanisms of infecting viruses to stall host cell death give a new dimension to the viral infection process. However, plant cell death profiles provide an entirely different scenario. The presence of a cell wall that cannot be phagocytosed, absence of the hallmarks of animal PCDs such as DNA laddering, formation of apoptotic bodies, a cell-death-specific nuclease, a biochemical machinery of killer enzymes such as caspases all point to novel ways of cell elimination. Large gaps in our understanding of plant cell death have prompted speculative inferences and comparisons with animal cell death mechanisms. This paper deals with both animals and plants for a holistic view on cell death in eukaryotes. © 2001 Academic Press.
引用
收藏
页码:159 / 242
页数:84
相关论文
共 367 条
[1]   Homology and developmental genes [J].
Abouheif, E ;
Akam, M ;
Dickinson, WJ ;
Holland, PWH ;
Meyer, A ;
Patel, NH ;
Raff, RA ;
Roth, VL ;
Wray, GA .
TRENDS IN GENETICS, 1997, 13 (11) :432-433
[2]  
ABRAMS JM, 1993, DEVELOPMENT, V117, P29
[3]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[4]   APOPTOSIS - A GENERAL COMMENT [J].
ALLES, A ;
ALLEY, K ;
BARRETT, JC ;
BUTTYAN, R ;
COLUMBANO, A ;
COPE, FO ;
COPELAN, EA ;
DUKE, RC ;
FAREL, PB ;
GERSHENSON, LE ;
GOLDGABER, D ;
GREEN, DR ;
HONN, KV ;
HULLY, J ;
ISAACS, JT ;
KERR, JFR ;
KRAMMER, PH ;
LOCKSHIN, RA ;
MARTIN, DP ;
MCCONKEY, DJ ;
MICHAELSON, J ;
SCHULTEHERMANN, R ;
SERVER, AC ;
SZENDE, B ;
TOMEI, LD ;
TRITTON, TR ;
UMANSKY, SR ;
VALERIE, K ;
WARNER, HR .
FASEB JOURNAL, 1991, 5 (08) :2127-2128
[5]   Involvement of p53 in cell differentiation and development [J].
Almog, N ;
Rotter, V .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1997, 1333 (01) :F1-F27
[6]   The domains of death: evolution of the apoptosis machinery [J].
Aravind, L ;
Dixit, VM ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (02) :47-53
[7]   Tumor necrosis factor receptor-associated factors (TRAFs) - a family of adaptor proteins that regulates life and death [J].
Arch, RH ;
Gedrich, RW ;
Thompson, CB .
GENES & DEVELOPMENT, 1998, 12 (18) :2821-2830
[8]   Apoptosis control by death and decoy receptors [J].
Ashkenazi, A ;
Dixit, VM .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (02) :255-260
[9]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[10]   P53 BINDS SINGLE-STRANDED-DNA ENDS THROUGH THE C-TERMINAL DOMAIN AND INTERNAL DNA SEGMENTS VIA THE MIDDLE DOMAIN [J].
BAKALKIN, G ;
SELIVANOVA, G ;
YAKOVLEVA, T ;
KISELEVA, E ;
KASHUBA, E ;
MAGNUSSON, KP ;
SZEKELY, L ;
KLEIN, G ;
TERENIUS, L ;
WIMAN, KG .
NUCLEIC ACIDS RESEARCH, 1995, 23 (03) :362-369