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RCS1, a substrate of APC/C, controls the metaphase to anaphase transition

机译:RCS1是APC / C的底物,控制中期到后期的过渡

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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 RC51 fluctuate in the cell cycle, peaking in mitosis and dropping drastically as cells exit into G_1. lndeed, 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.
机译:促进后期的复合物/环体(APC / C)通过靶向破坏姜黄素来控制后期的发作。我们在这里报告的鉴定和表征的APC / C,RCS1,作为控制中期和后期过渡的有丝分裂调节剂的底物。我们显示,RC51的水平在细胞周期中波动,在有丝分裂中达到峰值,并随着细胞进入G_1而急剧下降。实际上,RCS1在体外被APC / C有效泛素化,并在体内以Cdh1依赖性方式在有丝分裂退出期间降解。 APC / C在RCS1的N端识别一个独特的D-box,因为该D-box的突变在体外消除了泛素化作用,并在体内稳定了突变蛋白。 RCS1控制后期发生的时间,因为RCS1的丢失导致从中期到后期的快速发展,并加速了安胎蛋白和细胞周期蛋白B的降解。从生化角度看,有丝分裂的RCS1与NuRD染色质重塑复合物相关,并且这种RCS1复合物可能参与调节基因表达或染色质结构,进而控制后期发生。我们的研究发现了从中期到后期过渡的复杂调控网络。

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