McIntosh J R, Euteneuer U
J Cell Biol. 1984 Feb;98(2):525-33. doi: 10.1083/jcb.98.2.525.
The structural polarity of cellular microtubules can be visualized in situ by lysing cells in special buffers containing tubulin. Under these conditions, the tubulin polymerizes to form curved sheets which attach to the walls of the endogenous microtubules. When such decorated microtubules are cut in cross section and viewed in the electron microscope, they appear to bear hooks curving clockwise or counter-clockwise. The direction of hook curvature is defined by the orientation of the decorated microtubule and thus serves as a probe for microtubule polarity. In this paper we describe a way to analyze the relative frequencies of hooks of different curvatures so as to measure the fidelity of the relation between hook curvature and microtubule polarity. The assumptions of the method are tested and found to be valid to a reasonable accuracy. The correlation between hook curvature and microtubule orientation is shown to be at least 0.98 for the spindles of PtK cells and Haemanthus endosperm at all stages of division and at all places in the spindle. The correlation is shown to be valid for each hook that forms, so the polarity of those microtubules that bear multiple hooks is specified with even better certainty than 0.98. This property of hook decoration is used to reinvestigate the possibility that some of the microtubules of the kinetochore fiber might be oriented with their plus ends distal to the kinetochore (opposite to the direction previously shown to predominate). Close analysis fails to identify such oppositely oriented microtubules. The scoring of tubules bearing multiple hooks also shows that individual interzone fibers at anaphase are constructed from clusters of antiparallel microtubules. The method for estimating the correlation between hook decoration and microtubule polarity is shown to be applicable to many structures and circumstances, but we find that the hook decoration assay for microtubule polarity is not uniformly accurate. We suggest that future studies using hook decorations should employ the method of data analysis presented here to assess the accuracy of the results obtained.
细胞微管的结构极性可通过在含有微管蛋白的特殊缓冲液中裂解细胞来原位观察。在这些条件下,微管蛋白聚合形成弯曲的薄片,附着在内源微管的壁上。当这种装饰后的微管被切成横截面并在电子显微镜下观察时,它们似乎带有顺时针或逆时针弯曲的钩。钩的弯曲方向由装饰后的微管的方向决定,因此可作为微管极性的探针。在本文中,我们描述了一种分析不同曲率的钩的相对频率的方法,以便测量钩曲率与微管极性之间关系的保真度。该方法的假设经过测试,发现具有合理的准确性。对于PtK细胞纺锤体和海红豆胚乳在分裂的所有阶段以及纺锤体的所有位置,钩曲率与微管方向之间的相关性至少为0.98。对于形成的每个钩,这种相关性都是有效的,因此带有多个钩的那些微管的极性可以更确定地指定,确定性超过0.98。钩装饰的这一特性被用于重新研究动粒纤维的一些微管可能以其正端远离动粒的方向排列(与先前显示为主导的方向相反)的可能性。仔细分析未能识别出这种反向排列的微管。对带有多个钩的微管进行评分还表明,后期的单个中间区纤维是由反平行微管簇构成的。估计钩装饰与微管极性之间相关性的方法被证明适用于许多结构和情况,但我们发现用于微管极性的钩装饰测定并不总是准确的。我们建议未来使用钩装饰的研究应采用本文提出的数据分析方法来评估所获得结果的准确性。