Leaving no-one behind: how CENP-E facilitates chromosome alignment

被引:31
|
作者
Craske, Benjamin [1 ]
Welburn, Julie P. I. [1 ]
机构
[1] Univ Edinburgh, Sch Biol Sci, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3BF, Midlothian, Scotland
来源
基金
英国生物技术与生命科学研究理事会;
关键词
SPINDLE CHECKPOINT PROTEINS; PUTATIVE KINETOCHORE MOTOR; MICROTUBULE CAPTURE; MITOTIC CHECKPOINT; HELA-CELLS; KINESIN MOTOR; RZZ COMPLEX; CONGRESSION; END; ATTACHMENT;
D O I
10.1042/EBC20190073
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chromosome alignment and biorientation is essential for mitotic progression and genomic stability. Most chromosomes align at the spindle equator in a motor-independent manner. However, a subset of polar kinetochores fail to bi-orient and require a microtubule motor-based transport mechanism to move to the cell equator. Centromere Protein E (CENP-E/KIF10) is a kinesin motor from the Kinesin-7 family, which localizes to unattached kinetochores during mitosis and utilizes plus-end directed microtubule motility to slide mono-oriented chromosomes to the spindle equator. Recent work has revealed how CENP-E cooperates with chromokinesins and dynein to mediate chromosome congression and highlighted its role at aligned chromosomes. Additionally, we have gained new mechanistic insights into the targeting and regulation of CENP-E motor activity at the kinetochore. Here, we will review the function of CENP-E in chromosome congression, the pathways that contribute to CENP-E loading at the kinetochore, and how CENP-E activity is regulated during mitosis.
引用
收藏
页码:313 / 324
页数:12
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