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Polo样激酶1:后期促进复合物/细胞周期体依赖性蛋白水解的靶点与调节因子

Polo-like kinase 1: target and regulator of anaphase-promoting complex/cyclosome-dependent proteolysis.

作者信息

Eckerdt Frank, Strebhardt Klaus

机构信息

Department of Pharmacology, University of Colorado School of Medicine, Denver, Colorado 80262, USA.

出版信息

Cancer Res. 2006 Jul 15;66(14):6895-8. doi: 10.1158/0008-5472.CAN-06-0358.

Abstract

Polo-like kinase 1 (Plk1) is a key regulator of progression through mitosis. Although Plk1 seems to be dispensable for entry into mitosis, its role in spindle formation and exit from mitosis is crucial. Recent evidence suggests that a major role of Plk1 in exit from mitosis is the regulation of inhibitors of the anaphase-promoting complex/cyclosome (APC/C), such as the early mitotic inhibitor 1 (Emi1) and spindle checkpoint proteins. Thus, Plk1 and the APC/C control mitotic regulators by both phosphorylation and targeted ubiquitylation to ensure the fidelity of chromosome separation at the metaphase to anaphase transition. The mechanisms underlying the control of genomic stability by Plk1 are discussed in this review.

摘要

Polo样激酶1(Plk1)是有丝分裂进程的关键调节因子。虽然Plk1对于进入有丝分裂似乎并非必不可少,但其在纺锤体形成和退出有丝分裂过程中的作用至关重要。最近的证据表明,Plk1在退出有丝分裂中的主要作用是调节后期促进复合物/环体(APC/C)的抑制剂,如早期有丝分裂抑制剂1(Emi1)和纺锤体检查点蛋白。因此,Plk1和APC/C通过磷酸化和靶向泛素化来控制有丝分裂调节因子,以确保在中期到后期过渡时染色体分离的准确性。本文综述了Plk1控制基因组稳定性的潜在机制。

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