激酶-8马达在细胞周期中的作用和调控。

Systems and Synthetic Biology Pub Date : 2014-09-01 Epub Date: 2014-03-23 DOI:10.1007/s11693-014-9140-z
Liam J Messin, Jonathan B A Millar
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引用次数: 20

摘要

在整个真核细胞周期中,激酶-8马达家族的成员在控制微管长度方面发挥着核心作用。肌动蛋白-8失活会导致间期、星状体和有丝分裂纺锤体长度、中期染色体排列、后期开始的时间和染色体分离的准确性等细胞极性缺陷。虽然动力学蛋白8分子影响微管动力学的生物物理机制已经在各种物种中得到了广泛的研究,但尚未形成共识。其中一个原因可能是激酶-8家族的一些成员可以与其他微管相关蛋白、细胞周期调节蛋白和其他激酶家族成员结合。在这篇综述中,我们考虑了细胞周期特异性修饰及其与其他调节蛋白的关联如何调节激酶-8的功能,使其成为微管动力学的主要调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Role and regulation of kinesin-8 motors through the cell cycle.

Members of the kinesin-8 motor family play a central role in controlling microtubule length throughout the eukaryotic cell cycle. Inactivation of kinesin-8 causes defects in cell polarity during interphase and astral and mitotic spindle length, metaphase chromosome alignment, timing of anaphase onset and accuracy of chromosome segregation. Although the biophysical mechanism by which kinesin-8 molecules influence microtubule dynamics has been studied extensively in a variety of species, a consensus view has yet to emerge. One reason for this might be that some members of the kinesin-8 family can associate to other microtubule-associated proteins, cell cycle regulatory proteins and other kinesin family members. In this review we consider how cell cycle specific modification and its association to other regulatory proteins may modulate the function of kinesin-8 to enable it to function as a master regulator of microtubule dynamics.

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