Tubulin isotypes contribute opposing properties to balance anaphase spindle morphogenesis.

IF 6.4 1区 生物学 Q1 CELL BIOLOGY
Journal of Cell Biology Pub Date : 2025-09-01 Epub Date: 2025-07-25 DOI:10.1083/jcb.202301115
Emmanuel T Nsamba, Abesh Bera, Vaishali Todi, Landon Savoy, Ryan M Gupta, Mohan L Gupta
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引用次数: 0

Abstract

Faithful chromosome segregation requires proper function of the mitotic spindle, which is built from, and depends on, the coordinated regulation of many microtubules and the activities of molecular motors and MAPs. In addition, microtubules themselves are assembled from multiple variants, or isotypes of α- and β-tubulin, yet whether they mediate the activities of motors and MAPs required for proper spindle function remains poorly understood. Here, we use budding yeast to reveal that α-tubulin isotypes regulate opposing outward- and inward-directed forces in the spindle midzone that facilitate optimal spindle elongation and length control. Moreover, we show that the isotypes mediate balanced spindle forces by differentially localizing the antagonistic force generators Cin8 (kinesin-5) and Kar3 (kinesin-14) to interpolar microtubules. Our results reveal new roles for tubulin isotypes in orchestrating motor and MAP activities and provide insights into how forces in the spindle are properly calibrated to ensure proper mitotic spindle morphogenesis.

微管蛋白同型贡献相反的特性来平衡后期纺锤体形态发生。
忠实的染色体分离需要有丝分裂纺锤体的正常功能,而有丝分裂纺锤体是由许多微管的协调调节以及分子马达和map的活动建立和依赖的。此外,微管本身由α-和β-微管蛋白的多种变体或同型组合而成,但它们是否介导纺锤体正常功能所需的马达和map的活动仍然知之甚少。在这里,我们利用出芽酵母揭示了α-微管蛋白同型调节纺锤体中间区相反的外向和内向力,从而促进纺锤体的最佳伸长和长度控制。此外,我们还表明,这些同型体通过将拮抗力产生因子Cin8 (kinesin-5)和Kar3 (kinesin-14)不同地定位到极性微管中来调节平衡的纺锤力。我们的研究结果揭示了微管蛋白同型在协调运动和MAP活动中的新作用,并提供了如何正确校准纺锤体中的力以确保正确的有丝分裂纺锤体形态发生的见解。
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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来源期刊
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
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