Chen P, Rodriguez A, Erskine R, Thach T, Abrams J M
Department of Cell Biology and Neuroscience, University of Texas, Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75235-9039, USA.
Dev Biol. 1998 Sep 15;201(2):202-16. doi: 10.1006/dbio.1998.9000.
Caspases are widely conserved proteases considered to be essential effectors of apoptosis. We identified a novel Drosophila gene, dredd, which shares extensive homology to all members of the caspase gene family. Cells specified for programmed death in development exhibit a striking accumulation of dredd RNA that requires signaling by the death activators REAPER, GRIM, and HID. Furthermore, directed misexpression of each activator was sufficient to drive ectopic accumulation of dredd RNA. Heterozygosity at the dredd locus suppressed apoptosis in transgenic models of reaper- and grim-induced cell killing, demonstrating that levels of dredd product can modulate signaling triggered by these death activators. Finally, expression of REAPER, GRIM, and HID was found to trigger processing of DREDD protein precursor through a mechanism that is insensitive to, and upstream of, known caspase inhibitors. Taken together, these observations establish mechanistic connections between activators of apoptosis and a new downstream death effector in Drosophila.
半胱天冬酶是广泛保守的蛋白酶,被认为是细胞凋亡的关键效应因子。我们鉴定出一个新的果蝇基因——dredd,它与半胱天冬酶基因家族的所有成员都有广泛的同源性。在发育过程中被指定进行程序性死亡的细胞会显著积累dredd RNA,这需要死亡激活因子REAPER、GRIM和HID发出信号。此外,每种激活因子的定向错误表达足以驱动dredd RNA的异位积累。在reaper和grim诱导细胞死亡的转基因模型中,dredd基因座的杂合性抑制了细胞凋亡,这表明dredd产物的水平可以调节由这些死亡激活因子触发的信号传导。最后,发现REAPER、GRIM和HID的表达通过一种对已知半胱天冬酶抑制剂不敏感且在其上游的机制触发DREDD蛋白前体的加工。综上所述,这些观察结果建立了果蝇细胞凋亡激活因子与一种新的下游死亡效应因子之间的机制联系。