Quinn Leonie, Coombe Michelle, Mills Kathryn, Daish Tasman, Colussi Paul, Kumar Sharad, Richardson Helena
Trescowick Research Laboratories, Peter MacCallum Cancer Institute, St Andrews Place, East Melbourne.
EMBO J. 2003 Jul 15;22(14):3568-79. doi: 10.1093/emboj/cdg355.
Bcl-2 family proteins are key regulators of apoptosis. Both pro-apoptotic and anti-apoptotic members of this family are found in mammalian cells, but only the pro-apoptotic protein Debcl has been characterized in Drosophila: Here we report that Buffy, the second Drosophila Bcl-2-like protein, is a pro-survival protein. Ablation of Buffy by RNA interference leads to ectopic apoptosis, whereas overexpression of buffy results in the inhibition of developmental programmed cell death and gamma irradiation-induced apoptosis. Buffy interacts genetically and physically with Debcl to suppress Debcl-induced cell death. Genetic interactions suggest that Buffy acts downstream of Rpr, Grim and Hid, and upstream of the apical caspase Dronc. Furthermore, overexpression of buffy inhibits ectopic cell death in diap1 (th(5)) mutants. Taken together these data suggest that Buffy can act downstream of Rpr, Grim and Hid to block caspase-dependent cell death. Overexpression of Buffy in the embryo results in inhibition of the cell cycle, consistent with a G(1)/early-S phase arrest. Our data suggest that Buffy is functionally similar to the mammalian pro-survival Bcl-2 family of proteins.
Bcl-2家族蛋白是细胞凋亡的关键调节因子。该家族的促凋亡和抗凋亡成员都存在于哺乳动物细胞中,但在果蝇中仅鉴定出促凋亡蛋白Debcl:在此我们报告,果蝇的第二个Bcl-2样蛋白Buffy是一种促生存蛋白。通过RNA干扰消除Buffy会导致异位凋亡,而Buffy的过表达则会抑制发育性程序性细胞死亡和γ射线诱导的凋亡。Buffy与Debcl在遗传和物理上相互作用,以抑制Debcl诱导的细胞死亡。遗传相互作用表明,Buffy作用于Rpr、Grim和Hid的下游,以及顶端半胱天冬酶Dronc的上游。此外,Buffy的过表达抑制了diap1(th(5))突变体中的异位细胞死亡。综合这些数据表明,Buffy可以作用于Rpr、Grim和Hid的下游,以阻断半胱天冬酶依赖性细胞死亡。Buffy在胚胎中的过表达导致细胞周期的抑制,这与G(1)/早期S期停滞一致。我们的数据表明,Buffy在功能上类似于哺乳动物促生存的Bcl-2家族蛋白。