Martins Torcato, Meghini Francesco, Florio Francesca, Kimata Yuu
Cell Cycle Development Group, Department of Genetics, University of Cambridge, Cambridge CB2 3EH, UK.
Cell Cycle Development Group, Department of Genetics, University of Cambridge, Cambridge CB2 3EH, UK.
Dev Cell. 2017 Jan 9;40(1):67-80. doi: 10.1016/j.devcel.2016.12.005. Epub 2016 Dec 29.
The cell cycle is coordinated with differentiation during animal development. Here we report a cell-cycle-independent developmental role for a master cell-cycle regulator, the anaphase-promoting complex or cyclosome (APC/C), in the regulation of cell fate through modulation of Wingless (Wg) signaling. The APC/C controls both cell-cycle progression and postmitotic processes through ubiquitin-dependent proteolysis. Through an RNAi screen in the developing Drosophila eye, we found that partial APC/C inactivation severely inhibits retinal differentiation independently of cell-cycle defects. The differentiation inhibition coincides with hyperactivation of Wg signaling caused by the accumulation of a Wg modulator, Drosophila Nek2 (dNek2). The APC/C degrades dNek2 upon synchronous G1 arrest prior to differentiation, which allows retinal differentiation through local suppression of Wg signaling. We also provide evidence that decapentaplegic signaling may posttranslationally regulate this APC/C function. Thus, the APC/C coordinates cell-fate determination with the cell cycle through the modulation of developmental signaling pathways.
在动物发育过程中,细胞周期与细胞分化相互协调。在此,我们报告了一种主要的细胞周期调节因子——后期促进复合物或细胞周期体(APC/C)在细胞命运调控中不依赖于细胞周期的发育作用,它通过调节无翅(Wg)信号来实现这一调控。APC/C通过泛素依赖性蛋白水解作用控制细胞周期进程和有丝分裂后过程。通过在发育中的果蝇眼睛中进行RNA干扰筛选,我们发现部分APC/C失活会严重抑制视网膜分化,且与细胞周期缺陷无关。这种分化抑制与由Wg调节因子果蝇Nek2(dNek2)积累导致的Wg信号过度激活相一致。在分化前同步的G1期停滞时,APC/C会降解dNek2,从而通过局部抑制Wg信号实现视网膜分化。我们还提供了证据表明,骨形态发生蛋白信号可能在翻译后调节这种APC/C功能。因此,APC/C通过调节发育信号通路,将细胞命运决定与细胞周期协调起来。