Zhao Wei-Meng, Coppinger Judith A, Seki Akiko, Cheng Xiao-Li, Yates John R, Fang Guowei
Department of Biological Sciences, Stanford University, Stanford, CA 94305-5020, USA.
Proc Natl Acad Sci U S A. 2008 Sep 9;105(36):13415-20. doi: 10.1073/pnas.0709227105. Epub 2008 Aug 29.
The anaphase-promoting complex/cyclosome (APC/C) controls the onset of anaphase by targeting securin for destruction. We report here the identification and characterization of a substrate of APC/C, RCS1, as a mitotic regulator that controls the metaphase-to-anaphase transition. We showed that the levels of RCS1 fluctuate in the cell cycle, peaking in mitosis and dropping drastically as cells exit into G(1). Indeed, RCS1 is efficiently ubiquitinated by APC/C in vitro and degraded during mitotic exit in a Cdh1-dependent manner in vivo. APC/C recognizes a unique D-box at the N terminus of RCS1, as mutations of this D-box abolished ubiquitination in vitro and stabilized the mutant protein in vivo. RCS1 controls the timing of the anaphase onset, because the loss of RCS1 resulted in a faster progression from the metaphase to anaphase and accelerated degradation of securin and cyclin B. Biochemically, mitotic RCS1 associates with the NuRD chromatin-remodeling complex, and this RCS1 complex is likely involved in regulating gene expression or chromatin structure, which in turn may control anaphase onset. Our study uncovers a complex regulatory network for the metaphase-to-anaphase transition.
后期促进复合物/细胞周期体(APC/C)通过靶向切割蛋白进行降解来控制后期的起始。我们在此报告了APC/C的一个底物RCS1的鉴定和特征,它是一种控制中期到后期转变的有丝分裂调节因子。我们发现,RCS1的水平在细胞周期中波动,在有丝分裂期达到峰值,并在细胞进入G1期时急剧下降。实际上,RCS1在体外能被APC/C有效地泛素化,并在体内有丝分裂退出过程中以Cdh1依赖的方式降解。APC/C识别RCS1 N端一个独特的D盒,因为该D盒的突变消除了体外泛素化,并在体内使突变蛋白稳定。RCS1控制后期起始的时间,因为RCS1的缺失导致从中期到后期的进程加快,并加速了切割蛋白和细胞周期蛋白B的降解。从生化角度来看,有丝分裂期的RCS1与核小体重塑去乙酰化酶(NuRD)染色质重塑复合物结合,并且这个RCS1复合物可能参与调节基因表达或染色质结构,进而可能控制后期起始。我们的研究揭示了一个用于中期到后期转变的复杂调控网络。