Microtubule nucleation for spindle assembly: one molecule at a time

被引:15
作者
Kraus, Jodi [1 ]
Alfaro-Aco, Raymundo [1 ]
Gouveia, Bernardo [2 ]
Petry, Sabine [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ USA
关键词
GAMMA-TUBULIN COMPLEXES; CHROMOSOMAL PASSENGER COMPLEX; MITOTIC-SPINDLE; AURORA-B; INNER CENTROMERE; CENTROSOME MATURATION; SELF-ORGANIZATION; RING COMPLEX; PROTEIN; AUGMIN;
D O I
10.1016/j.tibs.2023.06.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cell orchestrates the dance of chromosome segregation with remarkable speed and fidelity. The mitotic spindle is built from scratch after interphase through microtubule (MT) nucleation, which is dependent on the gamma-tubulin ring complex (gamma-TuRC), the universal MT template. Although several MT nucleation pathways build the spindle framework, the question of when and how gamma-TuRC is targeted to these nucleation sites in the spindle and subsequently activated remains an active area of investigation. Recent advances facilitated the discovery of new MT nucleation effectors and their mechanisms of action. In this review, we illuminate each spindle assembly pathway and subsequently consider how the pathways are merged to build a spindle.
引用
收藏
页码:761 / 775
页数:15
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