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Parkin Regulates Mitosis and Genomic Stability through Cdc20/Cdh1

机译:Parkin通过Cdc20 / Cdh1调节有丝分裂和基因组稳定性

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Mutations in the E3 ubiquitin ligase Parkin have been linked to familial Parkinson's disease. Parkin has also been implicated in mitosis through mechanisms that are unclear. Here we show that Parkin interacts with anaphase promoting complex/cyclosome (APC/C) coactivators Cdc20 and Cdh1 to mediate the degradation of several key mitotic regulators independent of APC/C. We demonstrate that ordered progression through mitosis is orchestrated by two distinct E3 ligases through the shared use of Cdc20 and Cdh1. Furthermore, Parkin is phosphorylated and activated by polo-like kinase 1 (Plk1) during mitosis. Parkin deficiency results in overexpression of its substrates, mitotic defects, genomic instability, and tumorigenesis. These results suggest that the Parkin-Cdc20/Cdh1 complex is an important regulator of mitosis.
机译:E3泛素连接酶Parkin的突变与家族性帕金森氏病有关。帕金还通过不清楚的机制参与有丝分裂。在这里,我们显示帕金与后期促进复合物/环体(APC / C)共激活因子Cdc20和Cdh1相互作用,以介导几个独立于APC / C的关键有丝分裂调节剂的降解。我们证明通过有丝分裂的有序进展是由两个不同的E3连接酶通过共享使用Cdc20和Cdh1精心策划的。此外,在有丝分裂期间,Parkin被马球样激酶1(Plk1)磷酸化并激活。帕金缺乏症会导致其底物的过度表达,有丝分裂缺陷,基因组不稳定和肿瘤发生。这些结果表明,Parkin-Cdc20 / Cdh1复合物是有丝分裂的重要调节剂。

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