着丝点上Aurora A激酶的功能。

Jennifer G DeLuca
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引用次数: 7

摘要

染色体分离最重要的调控方面之一是着丝点精确控制其与纺锤体微管的附着强度的能力。这一调控的核心是极光B,一种有丝分裂激酶,使着丝点底物磷酸化以促进微管周转。Aurora B的一个关键靶点是着丝点蛋白Ndc80/Hec1,它是Ndc80复合物的一个组成部分,Ndc80复合物是着丝点和微管之间的主要力传导纽带。虽然Aurora B被认为是着丝点与微管连接的“主调节器”,但越来越清楚的是,这种激酶并不是唯一负责磷酸化Hec1和其他着丝点底物以促进微管周转的激酶。特别是,有越来越多的证据表明,在纺锤体极点的活动已经被广泛描述的极光激酶在着丝点中调节着丝点-微管界面具有额外的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aurora A Kinase Function at Kinetochores.

One of the most important regulatory aspects of chromosome segregation is the ability of kinetochores to precisely control their attachment strength to spindle microtubules. Central to this regulation is Aurora B, a mitotic kinase that phosphorylates kinetochore substrates to promote microtubule turnover. A critical target of Aurora B is the kinetochore protein Ndc80/Hec1, which is a component of the NDC80 complex, the primary force-transducing link between kinetochores and microtubules. Although Aurora B is regarded as the "master regulator" of kinetochore-microtubule attachment, it is becoming clear that this kinase is not solely responsible for phosphorylating Hec1 and other kinetochore substrates to facilitate microtubule turnover. In particular, there is growing evidence that Aurora A kinase, whose activities at spindle poles have been extensively described, has additional roles at kinetochores in regulating the kinetochore-microtubule interface.

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