星形有丝分裂纺锤体的形成:着丝体-着丝点相互作用的超微结构基础

Conly L. Rieder
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引用次数: 65

摘要

星形有丝分裂纺锤体的形成是在核膜破裂时开始的,这是由复制的纺锤体极点(即中心体)和染色体之间的相互作用引起的。由于这种相互作用,产生了微管束,这些微管束将每条染色体上的着丝点牢牢地附着在相反的纺锤极上。由于这些着丝点纤维也参与染色体的移动,因此它们形成的机制对于理解纺锤体内部产生力的病因至关重要。作为概述这种机制的前奏,纺锤体形成和染色体行为的动力学在活细胞中进行了检查。接下来,对着丝体和着丝点的性质进行了回顾,特别强调了细胞从间期过渡到有丝分裂时这些细胞器内发生的结构和功能变化。最后,一些最近的观察相关的机制,这些细胞器相互作用的详细和讨论。从这些不同的数据可以得出结论,着丝点纤维微管来源于动态不稳定的星体微管,这些星体微管生长在着丝点中,或生长在着丝点周围,然后与着丝点横向相互作用。此外,数据清楚地表明,单个星体微管与未附着染色体上的一个着丝点的相互作用足以使染色体附着在纺锤体上,使其朝向极点,并启动向极点运动。当染色体进入形成纺锤体区域时,更多的星体微管被纳入新生着丝点纤维中,染色体速度急剧下降。在此期间,梭形微管的分布从两个重叠的径向排列转变为中期细胞特征的梭形排列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formation of the astral mitotic spindle: Ultrastructural basis for the centrosome-kinetochore interaction

The formation of the astral mitotic spindle is initiated at the time of nuclear envelope breakdown from an interaction between the replicated spindle poles (i.e. centrosomes) and the chromosomes. As a result of this interaction bundles of microtubules are generated which firmly attach the kinetochores on each chromosome to opposite spindle poles. Since these kinetochore fibers are also involved in moving the chromosomes, the mechanism by which they are formed is of paramount importance to understanding the etiology of force production within the spindle. As a prelude to outlining such a mechanism, the dynamics of spindle formation and chromosome behavior are examined in the living cell. Next, the properties of centrosomes and kinetochores are reviewed with particular emphasis on the structural and functional changes that occur within these organelles as the cell transits from interphase to mitosis. Finally, a number of recent observations relevant to the mechanism by which these organelles interact are detailed and discussed. From these diverse data it can be concluded that kinetochore fiber microtubules are derived from dynamically unstable astral microtubules that grow into, or grow by and then interact laterally with, the kinetochore. Moreover, the data clearly demonstrate that the interaction of a single astral microtubule with one of the kinetochores on an unattached chromosome is sufficient to attach the chromosome to the spindle, orient it towards a pole, and initiate poleward motion. As the chromosomes move into the region of the forming spindle more astral microtubules become incorporated into the nascent kinetochore fibers and chromosome velocity decreases dramatically. During this time the distribution of spindle microtubules changes from two overlapping radial arrays to the fusiform array characteristic of metaphase cells.

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