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动粒处的激酶与磷酸酶相互作用

Kinase and Phosphatase Cross-Talk at the Kinetochore.

作者信息

Saurin Adrian T

机构信息

Jacqui Wood Cancer Centre, School of Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, United Kingdom.

出版信息

Front Cell Dev Biol. 2018 Jun 19;6:62. doi: 10.3389/fcell.2018.00062. eCollection 2018.

Abstract

Multiple kinases and phosphatases act on the kinetochore to control chromosome segregation: Aurora B, Mps1, Bub1, Plk1, Cdk1, PP1, and PP2A-B56, have all been shown to regulate both kinetochore-microtubule attachments and the spindle assembly checkpoint. Given that so many kinases and phosphatases converge onto two key mitotic processes, it is perhaps not surprising to learn that they are, quite literally, entangled in cross-talk. Inhibition of any one of these enzymes produces secondary effects on all the others, which results in a complicated picture that is very difficult to interpret. This review aims to clarify this picture by first collating the direct effects of each enzyme into one overarching schematic of regulation at the Knl1/Mis12/Ndc80 (KMN) network (a major signaling hub at the outer kinetochore). This schematic will then be used to discuss the implications of the cross-talk that connects these enzymes; both in terms of why it may be needed to produce the right type of kinetochore signals and why it nevertheless complicates our interpretations about which enzymes control what processes. Finally, some general experimental approaches will be discussed that could help to characterize kinetochore signaling by dissociating the direct from indirect effect of kinase or phosphatase inhibition . Together, this review should provide a framework to help understand how a network of kinases and phosphatases cooperate to regulate two key mitotic processes.

摘要

多种激酶和磷酸酶作用于动粒以控制染色体分离

极光激酶B(Aurora B)、Mps1、Bub1、Plk1、细胞周期蛋白依赖性激酶1(Cdk1)、蛋白磷酸酶1(PP1)和蛋白磷酸酶2A-B56,均已被证明可调节动粒与微管的附着以及纺锤体组装检查点。鉴于如此多的激酶和磷酸酶汇聚到两个关键的有丝分裂过程中,了解到它们实际上陷入了相互作用的混乱局面或许并不奇怪。抑制这些酶中的任何一种都会对其他所有酶产生次级效应,这导致了一幅非常难以解释的复杂图景。本综述旨在通过首先将每种酶的直接效应整理成一个关于Knl1/Mis12/Ndc80(KMN)网络(外动粒处的一个主要信号枢纽)调控的总体示意图来厘清这幅图景。然后,该示意图将被用于讨论连接这些酶的相互作用的影响;这既涉及为何可能需要这种相互作用来产生正确类型的动粒信号,也涉及为何它仍然使我们对哪些酶控制哪些过程的解释变得复杂。最后,将讨论一些通用的实验方法,这些方法有助于通过区分激酶或磷酸酶抑制的直接和间接效应来表征动粒信号传导。总之,本综述应提供一个框架,以帮助理解激酶和磷酸酶网络如何协同调节两个关键的有丝分裂过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0193/6018199/7625339f8df2/fcell-06-00062-g0001.jpg

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