Joined at the hip: kinetochores, microtubules, and spindle assembly checkpoint signaling

被引:135
|
作者
Sacristan, Carlos [1 ]
Kops, Geert J. P. L. [1 ,2 ,3 ]
机构
[1] Univ Med Ctr Utrecht, NL-3584 CG Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Ctr Mol Med, NL-3584 CG Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Canc Genom Netherlands, NL-3584 CG Utrecht, Netherlands
基金
欧洲研究理事会;
关键词
kinetochore; spindle; checkpoint; aneuploidy; microtubule; PROTEIN PHOSPHATASE 1; MITOTIC CHECKPOINT; AURORA-B; CENP-E; UNATTACHED KINETOCHORES; CHROMOSOME CONGRESSION; OUTER KINETOCHORE; MPS1; ACTIVATION; BUB3; STABILITY; MPH1; KINASE;
D O I
10.1016/j.tcb.2014.08.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Error-free chromosome segregation relies on stable connections between kinetochores and spindle microtubules. The spindle assembly checkpoint (SAC) monitors such connections and relays their absence to the cell cycle machinery to delay cell division. The molecular network at kinetochores that is responsible for microtubule binding is integrated with the core components of the SAC signaling system. Molecular-mechanistic understanding of how the SAC is coupled to the kinetochore microtubule interface has advanced significantly in recent years. The latest insights not only provide a striking view of the dynamics and regulation of SAC signaling events at the outer kinetochore but also create a framework for understanding how that signaling may be terminated when kinetochores and microtubules connect.
引用
收藏
页码:21 / 28
页数:8
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