Mitotic spindle assembly in animal cells: a fine balancing act

被引:276
作者
Prosser, Suzanna L. [1 ,2 ]
Pelletier, Laurence [1 ,3 ]
机构
[1] Sinai Hlth Syst, Lunenfeld Tanenbaum Res Inst, 600 Univ Ave, Toronto, ON M5G 1X5, Canada
[2] Natl Univ Ireland Galway, Ctr Chromosome Biol, Sch Nat Sci, Galway H91 TK33, Ireland
[3] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
基金
加拿大自然科学与工程研究理事会; 欧盟地平线“2020”;
关键词
CHROMOSOMAL PASSENGER COMPLEX; XENOPUS EGG EXTRACTS; KINETOCHORE FIBERS CONTRIBUTES; MICROTUBULE-BINDING SITE; DROSOPHILA S2 CELLS; MOTOR PROTEINS; MINUS ENDS; AURORA-A; RANGTP GRADIENT; SOMATIC-CELLS;
D O I
10.1038/nrm.2016.162
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mitotic spindle has a crucial role in ensuring the accurate segregation of chromosomes into the two daughter cells during cell division, which is paramount for maintaining genome integrity. It is a self-organized and dynamic macromolecular structure that is constructed from microtubules, microtubule-associated proteins and motor proteins. Thirty years of research have led to the identification of centrosome-, chromatin-and microtubule-mediated microtubule nucleation pathways that each contribute to mitotic spindle assembly. Far from being redundant pathways, data are now emerging regarding how they function together to ensure the timely completion of mitosis. We are also beginning to comprehend the multiple mechanisms by which cells regulate spindle scaling. Together, this research has increased our understanding of how cells coordinate hundreds of proteins to assemble the dynamic, precise and robust structure that is the mitotic spindle.
引用
收藏
页码:187 / 201
页数:15
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