Tapon Nicolas, Harvey Kieran F, Bell Daphne W, Wahrer Doke C R, Schiripo Taryn A, Haber Daniel A, Hariharan Iswar K
Massachusetts General Hospital Cancer Center, Building 149, 13th Street, Charlestown 02129, USA.
Cell. 2002 Aug 23;110(4):467-78. doi: 10.1016/s0092-8674(02)00824-3.
The number of cells in an organism is determined by regulating both cell proliferation and cell death. Relatively few mechanisms have been identified that can modulate both of these processes. In a screen for Drosophila mutations that result in tissue overgrowth, we identified salvador (sav), a gene that promotes both cell cycle exit and cell death. Elevated Cyclin E and DIAP1 levels are found in mutant cells, resulting in delayed cell cycle exit and impaired apoptosis. Salvador contains two WW domains and binds to the Warts (or LATS) protein kinase. The human ortholog of salvador (hWW45) is mutated in three cancer cell lines. Thus, salvador restricts cell numbers in vivo by functioning as a dual regulator of cell proliferation and apoptosis.
生物体中的细胞数量是通过调节细胞增殖和细胞死亡来确定的。目前已确定的能够调节这两个过程的机制相对较少。在一项针对导致组织过度生长的果蝇突变体的筛选中,我们发现了“救星”(sav)基因,它既能促进细胞周期退出,又能促进细胞死亡。在突变细胞中发现细胞周期蛋白E和DIAP1水平升高,导致细胞周期退出延迟和细胞凋亡受损。“救星”含有两个WW结构域,并与疣蛋白激酶(或大肿瘤抑制激酶1)结合。“救星”的人类同源物(hWW45)在三种癌细胞系中发生了突变。因此,“救星”通过作为细胞增殖和凋亡的双重调节因子来限制体内细胞数量。