SAC如何得到斧头:整合着丝点微管附着物与纺锤体组装检查点信号。

Bioarchitecture Pub Date : 2015-01-01 Epub Date: 2015-10-02 DOI:10.1080/19490992.2015.1090669
Shivangi Agarwal, Dileep Varma
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引用次数: 6

摘要

有丝分裂需要复制染色体的真正分离。这一过程是通过染色体上的着丝点附着在有丝分裂纺锤体的微管(mt)上完成的。一旦获得适当的附着,需要使延迟后期过早开始的纺锤体组装检查点(SAC)沉默,以便细胞进入后期和细胞质分裂。因此,虽然在着丝点未附着时保存SAC是必要的,但在着丝点微管(kMT)附着后去除SAC成分是至关重要的。关于kMT附着体如何触发SAC组分从着丝点移除,以及检查点蛋白如何反馈到附着机制的精确知识仍然是难以捉摸的。这篇综述的目的是描述最近的进展,提供了一个洞察分子事件的相互作用,协调和调节SAC活性响应于细胞分裂期间的kMT附着。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

How the SAC gets the axe: Integrating kinetochore microtubule attachments with spindle assembly checkpoint signaling.

How the SAC gets the axe: Integrating kinetochore microtubule attachments with spindle assembly checkpoint signaling.

How the SAC gets the axe: Integrating kinetochore microtubule attachments with spindle assembly checkpoint signaling.

Mitosis entails the bona fide segregation of duplicated chromosomes. This process is accomplished by the attachment of kinetochores on chromosomes to microtubules (MTs) of the mitotic spindle. Once the appropriate attachment is achieved, the spindle assembly checkpoint (SAC) that delays the premature onset of anaphase needs to be silenced for the cell to proceed to anaphase and cytokinesis. Therefore, while it is imperative to preserve the SAC when kinetochores are unattached, it is of paramount importance that SAC components are removed post kinetochore microtubule (kMT) attachment. Precise knowledge of how kMT attachments trigger the removal of SAC components from kinetochores or how the checkpoint proteins feedback in to the attachment machinery remains elusive. This review aims to describe the recent advances that provide an insight into the interplay of molecular events that coordinate and regulate the SAC activity in response to kMT attachment during cell division.

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