Dept. of Molecular, Cellular, and Developmental Biology University of Colorado, Boulder, CO 80309-0347, USA.
Semin Cell Dev Biol. 2021 Sep;117:118-126. doi: 10.1016/j.semcdb.2021.03.009. Epub 2021 Mar 26.
Anaphase A is the motion of recently separated chromosomes to the spindle pole they face. It is accompanied by the shortening of kinetochore-attached microtubules. The requisite tubulin depolymerization may occur at kinetochores, at poles, or both, depending on the species and/or the time in mitosis. These depolymerization events are local and suggest that cells regulate microtubule dynamics in specific places, presumably by the localization of relevant enzymes and microtubule-associated proteins to specific loci, such as pericentriolar material and outer kinetochores. Motor enzymes can contribute to anaphase A, both by altering microtubule stability and by pushing or pulling microtubules through the cell. The generation of force on chromosomes requires couplings that can both withstand the considerable force that spindles can generate and simultaneously permit tubulin addition and loss. This chapter reviews literature on the molecules that regulate anaphase microtubule dynamics, couple dynamic microtubules to kinetochores and poles, and generate forces for microtubule and chromosome motion.
后期 A 是指最近分离的染色体向其面对的纺锤体极运动。它伴随着动粒附着的微管缩短。必要的微管解聚可能发生在动粒、极或两者都发生,这取决于物种和/或有丝分裂中的时间。这些解聚事件是局部的,表明细胞在特定位置调节微管动力学,可能通过将相关酶和微管相关蛋白定位到特定的位置,如中心粒周围物质和外动粒来实现。马达酶可以通过改变微管稳定性和通过推动或拉动微管穿过细胞来促进后期 A。染色体上的力生成需要能够承受纺锤体产生的相当大的力的连接,同时允许微管添加和损失。本章回顾了调节后期微管动力学、将动态微管与动粒和极连接以及产生微管和染色体运动力的分子的文献。