Hyman A A, Mitchison T J
Department of Pharmacology, University of California, San Francisco 94143-0450.
J Cell Biol. 1990 May;110(5):1607-16. doi: 10.1083/jcb.110.5.1607.
The interface between kinetochores and microtubules in the mitotic spindle is known to be dynamic. Kinetochore microtubules can both polymerize and depolymerize, and their dynamic behavior is intimately related to chromosome movement. In this paper we investigate the influence of kinetochores on the inherent dynamic behavior of microtubules using an in vitro assay. The dynamics of microtubule plus ends attached to kinetochores are compared to those of free plus ends in the same solution. We show that microtubules attached to kinetochores exhibit the full range of dynamic instability behavior, but at altered transition rates. Surprisingly, we find that kinetochores increase the rate at which microtubule ends transit from growing to shrinking. This result contradicts our previous findings (Mitchison, T. J., and M. W. Kirschner, 1985b) for technical reasons which are discussed. We suggest that catalysis of the growing to shrinking transition by kinetochores may account for selective depolymerization of kinetochore microtubules during anaphase in vivo. We also investigate the effects of a nonhydrolyzable ATP analogue on kinetochore microtubule dynamics. We find that 5' adenylylimido diphosphate induces a rigor state at the kinetochore-microtubule interface, which prevents depolymerization of the microtubule.
有丝分裂纺锤体中动粒与微管之间的界面是动态的,这是已知的。动粒微管既能聚合也能解聚,其动态行为与染色体运动密切相关。在本文中,我们使用体外试验研究动粒对微管固有动态行为的影响。将附着在动粒上的微管正端的动态与同一溶液中自由正端的动态进行比较。我们发现,附着在动粒上的微管表现出完整的动态不稳定性行为,但转变速率有所改变。令人惊讶的是,我们发现动粒提高了微管末端从生长转变为收缩的速率。由于所讨论的技术原因,这一结果与我们之前的发现(米奇森,T. J.,和M. W. 基尔希纳,1985b)相矛盾。我们认为,动粒对生长到收缩转变的催化作用可能解释了体内后期动粒微管的选择性解聚。我们还研究了一种不可水解的ATP类似物对动粒微管动态的影响。我们发现,5'-腺苷酰亚胺二磷酸在动粒-微管界面诱导一种僵硬状态,从而阻止微管解聚。