A Kinase-Phosphatase Network that Regulates Kinetochore-Microtubule Attachments and the SAC.

Giulia Vallardi, Marilia Henriques Cordeiro, Adrian Thomas Saurin
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Abstract

The KMN network (for KNL1, MIS12 and NDC80 complexes) is a hub for signalling at the outer kinetochore. It integrates the activities of two kinases (MPS1 and Aurora B) and two phosphatases (PP1 and PP2A-B56) to regulate kinetochore-microtubule attachments and the spindle assembly checkpoint (SAC). We will first discuss each of these enzymes separately, to describe how they are regulated at kinetochores and why this is important for their primary function in controlling either microtubule attachments or the SAC. We will then discuss why inhibiting any one of them individually produces secondary effects on all the others. This cross-talk may help to explain why all enzymes have been linked to both processes, even though the direct evidence suggests they each control only one. This chapter therefore describes how a network of kinases and phosphatases work together to regulate two key mitotic processes.

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调控内转子-微管连接和 SAC 的激酶-磷酸酶网络
KMN 网络(KNL1、MIS12 和 NDC80 复合物)是外动转轴的信号枢纽。它整合了两种激酶(MPS1 和 Aurora B)和两种磷酸酶(PP1 和 PP2A-B56)的活动,以调节动子-微管连接和纺锤体组装检查点(SAC)。我们将首先分别讨论这些酶,描述它们在动点处的调控方式,以及为什么这对它们控制微管附着或 SAC 的主要功能非常重要。然后,我们将讨论为什么单独抑制其中任何一种酶都会对所有其他酶产生次要影响。这种交叉作用可能有助于解释为什么所有酶都与这两个过程有关,尽管直接证据表明它们各自只控制其中一个过程。因此,本章描述了激酶和磷酸酶网络如何共同调节两个关键的有丝分裂过程。
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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
7
期刊介绍: Molecular biology has been providing an overwhelming amount of data on the structural components and molecular machineries of the cell and its organelles and the complexity of intra- and intercellular communication. The molecular basis of hereditary and acquired diseases is beginning to be unravelled, and profound new insights into development and evolutionary biology have been gained from molecular approaches. Progress in Molecular and Subcellular Biology summarises the most recent developments in this fascinating area of biology.
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