grim, a novel cell death gene in Drosophila

被引:357
作者
Chen, P
Nordstrom, W
Gish, B
Abrams, JM
机构
[1] UNIV TEXAS, SW MED CTR, DEPT CELL BIOL & NEUROSCI, DALLAS, TX 75235 USA
[2] UNIV TEXAS, SW MED CTR, DEPT MOL BIOL & ONCOL, DALLAS, TX 75235 USA
关键词
apoptosis; programmed cell death; Drosophila;
D O I
10.1101/gad.10.14.1773
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A genomic interval at 75C1,2 is required for programmed cell death in Drosophila. We identified a new activator of apoptosis, grim, which maps between two previously identified cell death genes in this region reaper (rpr) and head involution defective (hid). Expression of grim RNA coincided with the onset of programmed cell death at all stages of embryonic development, whereas ectopic induction of grim triggered extensive apoptosis in both transgenic animals and in cell culture. Cell killing by grim was blocked by coexpression of p35, a viral product that inactivates ICE-like proteases, and did not require the functions of rpr or hid. The predicted grim protein shares an amino-terminal motif in common with rpr. However, grim was sufficient to elicit apoptosis in at least one context, where rpr was not. The grim gene product might thus function in a parallel circuit of cell death signaling that ultimately activates a common set of downstream apoptotic effecters.
引用
收藏
页码:1773 / 1782
页数:10
相关论文
共 59 条
[1]  
ABBOTT MK, 1991, GENETICS, V129, P783
[2]  
ABRAMS JM, 1993, DEVELOPMENT, V117, P29
[3]   MACROPHAGES IN DROSOPHILA EMBRYOS AND L2 CELLS EXHIBIT SCAVENGER RECEPTOR-MEDIATED ENDOCYTOSIS [J].
ABRAMS, JM ;
LUX, A ;
STELLER, H ;
KRIEGER, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10375-10379
[4]  
ABRAMS JM, 1996, APOPTOSIS NORMAL DEV, P171
[5]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[6]  
[Anonymous], 1993, MAKING FLY GENETICS
[7]  
Ashburner M., 1989, DROSOPHILA LAB MANUA
[8]   INHIBITION OF ICE FAMILY PROTEASES BY BACULOVIRUS ANTIAPOPTOTIC PROTEIN P35 [J].
BUMP, NJ ;
HACKETT, M ;
HUGUNIN, M ;
SESHAGIRI, S ;
BRADY, K ;
CHEN, P ;
FERENZ, C ;
FRANKLIN, S ;
GHAYUR, T ;
LI, P ;
LICARI, P ;
MANKOVICH, J ;
SHI, LF ;
GREENBERG, AH ;
MILLER, LK ;
WONG, WW .
SCIENCE, 1995, 269 (5232) :1885-1888
[9]   CHARACTERIZATION AND USE OF THE DROSOPHILA METALLOTHIONEIN PROMOTER IN CULTURED DROSOPHILA-MELANOGASTER CELLS [J].
BUNCH, TA ;
GRINBLAT, Y ;
GOLDSTEIN, LSB .
NUCLEIC ACIDS RESEARCH, 1988, 16 (03) :1043-1061
[10]  
Campos-Ortega J. A., 1997, The Embryonic Development of Drosophila melanogaster, Vsecond