Tippit D H, Schulz D, Pickett-Heaps J D
J Cell Biol. 1978 Dec;79(3):737-63. doi: 10.1083/jcb.79.3.737.
The spindle of the colonial diatom Fragilaria contains two distinct sets of spindle microtubules (MTs): (a) MTs comprising the central spindle, which is composed of two half-spindles interdigitated to form a region of "overlap"; (b) MTs which radiate laterally from the poles. The central spindles from 28 cells are reconstructed by tracking each MT of the central spindle through consecutive serial sections. Because the colonies of Fragilaria are flat ribbons of contiguous cells (clones), it is possible, by using single ribbons of cells, to compare reconstructed spindles at different mitotic stages with minimal intercellular variability. From these reconstructions we have determined: (a) the changes in distribution of MTs along the spindle during mitosis; (b) the change in the total number of MTs during mitosis; (c) the length of each MT (measured by the number of sections each traverses) at different mitotic stages; (d) the frequency of different classes of MTs (i.e., free, continuous, etc.); (e) the spatial arrangement of MTs from opposite poles in the overlap; (f) the approximate number of MTs, separate from the central spindle, which radiate from each spindle pole. From longitudinal sections of the central spindle, the lengths of the whole spindle, half-spindle, and overlap were measured from 80 cells at different mitotic stages. Numerous sources of error may create inaccuracies in these measurements; these problems are discussed. The central spindle at prophase consists predominantly of continuous MTs (pole to pole). Between late prophase and prometaphase, spindle length increases, and the spindle is transformed into two half-spindles (mainly polar MTs) interdigitated to form the overlap. At late anaphase-telophase, the overlap decreases concurrent with spindle elongation. Our interpretation is that the MTs of the central spindle slide past one another at both late prophase and late anaphase. These changes in MT distribution have the effect of elongating the spindle and are not involved in the poleward movement of the chromosomes. Some aspects of tracking spindle MTs, the interaction of MTs in the overlap, formation of the prophase spindle, and our interpretation of rearrangements of MTs, are discussed.
群居硅藻脆杆藻的纺锤体包含两组不同的纺锤体微管(MTs):(a)构成中央纺锤体的微管,中央纺锤体由两个相互交叉形成“重叠”区域的半纺锤体组成;(b)从纺锤体两极横向辐射的微管。通过在连续的系列切片中追踪中央纺锤体的每一根微管,重建了来自28个细胞的中央纺锤体。由于脆杆藻的群体是由相邻细胞(克隆)组成的扁平带,因此通过使用单个细胞带,可以在细胞间变异性最小的情况下比较不同有丝分裂阶段重建的纺锤体。从这些重建中我们确定了:(a)有丝分裂期间微管沿纺锤体分布的变化;(b)有丝分裂期间微管总数的变化;(c)不同有丝分裂阶段每根微管的长度(通过其穿过的切片数量测量);(d)不同类型微管(即游离的、连续的等)的频率;(e)重叠区域中来自相对两极的微管的空间排列;(f)从每个纺锤体极辐射出的、与中央纺锤体分开的微管的大致数量。从中央纺锤体的纵向切片中,测量了不同有丝分裂阶段80个细胞的整个纺锤体、半纺锤体和重叠区域的长度。这些测量中可能存在许多误差来源;对这些问题进行了讨论。前期的中央纺锤体主要由连续的微管(从极到极)组成。从前期末到前中期,纺锤体长度增加,纺锤体转变为两个相互交叉形成重叠区域的半纺锤体(主要是极微管)。在后期-末期,随着纺锤体伸长,重叠区域减小。我们的解释是,中央纺锤体的微管在晚前期和晚后期相互滑过。微管分布的这些变化起到了拉长纺锤体的作用,并且不参与染色体向极的移动。讨论了追踪纺锤体微管的一些方面、重叠区域中微管的相互作用、前期纺锤体的形成以及我们对微管重排的解释。