McIntosh J R, Roos U P, Neighbors B, McDonald K L
J Cell Sci. 1985 Apr;75:93-129. doi: 10.1242/jcs.75.1.93.
Ten mitotic spindles from Dictyostelium discoideum have been studied by electron microscopy of serial sections. We have used computer graphics to track individual microtubules (MTs) in three dimensions and to compare seven spindles at different stages of anaphase and telophase. The central spindle of early anaphase is formed by the interdigitation of two sets of pole-associated MTs. The distribution of MT lengths at this stage is hetero-disperse. During anaphase total MT length decreases by a factor of about 2 as a result of two opposing changes in MT length: the longer MTs that interdigitate become even longer, while the short MTs, including those attached to kinetochores, become shorter still and decrease in number. The extent of MT interdigitation is less in longer spindles than in short ones. In metaphase and early anaphase, the MTs are not in an ordered arrangement as seen in spindle cross-sections, but as anaphase proceeds the MTs cluster into a square-packed, paracrystalline bundle in which most of the nearest neighbours come from opposite poles. This arrangement and the condensation-like increase in order suggest the existence of specific interactions between antiparallel MTs. A quantitative analysis of MT positions supports this interpretation, but direct evidence for convincing bridges between MTs is lacking. The pole-distal ends of the MTs that interdigitate show an irregular termination (C-shaped ends in transverse view), as is characteristic of MTs that are either adding or losing subunits. Since it is these interdigitating MTs that elongate, and since the shortening MTs show the customary blunt endings, we conclude that subunits add to the interdigitating MTs at their pole-distal ends. This inference, combined with other structural data, suggests that the interdigitating MTs of Dictyostelium are sliding over one another as they polymerize in anaphase. It also suggests a simple model for why the spindle becomes thinner as it elongates. We propose that MT interdigitation defines a region where MTs bind a factor that will associate only with antiparallel MTs. This factor biases the MT assembly equilibrium toward polymer. As the shorter MTs slide out of this region, they lose their polymerization advantage and depolymerize, releasing subunits to contribute to the further elongation of the already longer MTs. The properties of the Dictyostelium spindle are compared with those of both higher and lower eukaryotes.
我们通过对盘基网柄菌的连续切片进行电子显微镜观察,研究了10个有丝分裂纺锤体。我们利用计算机图形技术在三维空间中追踪单个微管(MTs),并比较了处于后期和末期不同阶段的7个纺锤体。早期后期的中央纺锤体由两组与极相关的微管相互交错形成。此阶段微管长度的分布是异质分散的。在后期,由于微管长度的两种相反变化,微管总长度减少了约2倍:相互交错的较长微管变得更长,而短微管,包括那些附着在动粒上的微管,变得更短且数量减少。较长纺锤体中微管相互交错的程度比短纺锤体中的小。在中期和早期后期,如在纺锤体横切面上所见,微管并非有序排列,但随着后期的进行,微管聚集成一个方形堆积的准晶体束,其中大多数最近邻微管来自相对的两极。这种排列以及有序性类似凝聚的增加表明反平行微管之间存在特定相互作用。对微管位置的定量分析支持了这一解释,但缺乏令人信服的微管之间桥连的直接证据。相互交错的微管的极远端显示出不规则的末端(横切面上呈C形末端),这是正在添加或丢失亚基的微管的特征。由于正是这些相互交错的微管伸长,并且由于缩短的微管显示出通常的钝末端,我们得出结论,亚基在其极远端添加到相互交错的微管上。这一推断与其他结构数据相结合,表明盘基网柄菌的相互交错微管在后期聚合时相互滑动。这也为纺锤体在伸长时变细的原因提出了一个简单模型。我们提出微管相互交错定义了一个区域,在该区域微管结合一种仅与反平行微管结合的因子。这种因子使微管组装平衡偏向聚合物。随着较短的微管滑出该区域,它们失去聚合优势并解聚,释放亚基以促进已经较长的微管进一步伸长。将盘基网柄菌纺锤体的特性与高等和低等真核生物的特性进行了比较。