从一个错误的着丝细胞-微管附着状态的见解。

Bioarchitecture Pub Date : 2013-05-01 Epub Date: 2013-07-15 DOI:10.4161/bioa.25734
Stuart Cane, Philip T McGilvray, Thomas J Maresca
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引用次数: 3

摘要

基因组的忠实分布需要姐妹着丝点,它们在细胞分裂期间聚集在每个染色单体上,与来自相对纺锤体极点的动态微管相互作用,形成一种称为染色体双向的结构。双向定向产生张力,通过不明确的机制增加着丝点对微管的亲和力。非生物取向的着丝点-微管(kt-MT)相互作用普遍存在,但由于错误校正途径降低了着丝点对微管的亲和力,因此相互作用时间很短。有趣的是,不正确的kt-MT相互作用可以通过实验对错误定向的染色体施加力来稳定。在这里,活细胞力测定被用来表征一种常见类型的不适当的kt-MT附着的分子组成。我们的力相关研究也在当前的kt-MT相互作用的张力依赖稳定模型的背景下进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Insights from an erroneous kinetochore-microtubule attachment state.

Faithful distribution of the genome requires that sister kinetochores, which assemble on each chromatid during cell division, interact with dynamic microtubules from opposite spindle poles in a configuration called chromosome biorientation. Biorientation produces tension that increases the affinity of kinetochores for microtubules via ill-defined mechanisms. Non-bioriented kinetochore-microtubule (kt-MT) interactions are prevalent but short-lived due to an error correction pathway that reduces the affinity of kinetochores for microtubules. Interestingly, incorrect kt-MT interactions can be stabilized by experimentally applying force to misoriented chromosomes. Here, a live-cell force assay is utilized to characterize the molecular composition of a common type of improper kt-MT attachment. Our force-related studies are also discussed in the context of current models for tension-dependent stabilization of kt-MT interactions.

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