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Tubulin hooks as probes for microtubule polarity: an analysis of the method and an evaluation of data on microtubule polarity in the mitotic spindle

机译:小管钩作为微管极性的探针:有丝分裂纺锤体中微管极性的方法分析和数据评估

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摘要

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.
机译:通过在含有微管蛋白的特殊缓冲液中裂解细胞,可以原位观察细胞微管的结构极性。在这些条件下,微管蛋白聚合形成弯曲的薄片,该薄片附着在内源性微管的壁上。当将这样装饰的微管切开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子。钩弯曲的方向由装饰的微管的方向定义,因此用作微管极性的探针。在本文中,我们描述了一种分析不同曲率的钩子的相对频率的方法,以测量钩子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,并以合理的准确性被认为是有效的。在分裂的所有阶段以及在纺锤体的所有位置,PtK细胞纺锤体和风果胚乳的钩曲率与微管取向之间的相关性至少显示为0.98。该相关性对于形成的每个钩子都是有效的,因此带有多个钩子的那些微管的极性被指定为比0.98更好的确定性。钩形装饰的这种特性用于重新研究动线虫纤维的某些微管可能以其正端远离动线虫的方向(与先前显示的方向相反)定向的可能性。紧密分析未能鉴定出这种相反方向的微管。带有多个钩的小管的评分还表明,后期的单个区域间纤维是由反平行微管的簇构成的。钩形装饰与微管极性之间的相关性估计方法已显示适用于许多结构和环境,但我们发现,钩形装饰微管极性的测定方法并不一致。我们建议将来使用钩形装饰的研究应采用此处介绍的数据分析方法,以评估获得的结果的准确性。

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