Goyal L, McCall K, Agapite J, Hartwieg E, Steller H
Howard Hughes Medical Institute, Massachusetts Institute of Technology, Departments of Biology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
EMBO J. 2000 Feb 15;19(4):589-97. doi: 10.1093/emboj/19.4.589.
Induction of apoptosis in Drosophila requires the activity of three closely linked genes, reaper, hid and grim. Here we show that the proteins encoded by reaper, hid and grim activate cell death by inhibiting the anti-apoptotic activity of the Drosophila IAP1 (diap1) protein. In a genetic modifier screen, both loss-of-function and gain-of-function alleles in the endogenous diap1 gene were obtained, and the mutant proteins were functionally and biochemically characterized. Gain-of-function mutations in diap1 strongly suppressed reaper-, hid- and grim-induced apoptosis. Sequence analysis of these alleles revealed that they were caused by single amino acid changes in the baculovirus IAP repeat domains of diap1, a domain implicated in binding REAPER, HID and GRIM. Significantly, the corresponding mutant DIAP1 proteins displayed greatly reduced binding of REAPER, HID and GRIM, indicating that REAPER, HID and GRIM kill by forming a complex with DIAP1. These data provide strong in vivo evidence for a previously published model of cell death regulation in Drosophila.
在果蝇中诱导细胞凋亡需要三个紧密连锁的基因(收割者基因、hid基因和严峻基因)的活性。我们在此表明,收割者基因、hid基因和严峻基因所编码的蛋白质通过抑制果蝇IAP1(diap1)蛋白的抗凋亡活性来激活细胞死亡。在一项遗传修饰筛选中,获得了内源性diap1基因的功能丧失型和功能获得型等位基因,并对突变蛋白进行了功能和生化特性分析。diap1基因的功能获得型突变强烈抑制了收割者基因、hid基因和严峻基因诱导的细胞凋亡。对这些等位基因的序列分析表明,它们是由diap1的杆状病毒IAP重复结构域中的单个氨基酸变化引起的,该结构域与结合收割者蛋白、HID蛋白和严峻蛋白有关。值得注意的是,相应的突变型DIAP1蛋白与收割者蛋白、HID蛋白和严峻蛋白的结合显著减少,这表明收割者蛋白、HID蛋白和严峻蛋白通过与DIAP1形成复合物来引发细胞死亡。这些数据为先前发表的果蝇细胞死亡调控模型提供了强有力的体内证据。