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Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables

机译:酿酒酵母中的主轴取向取决于微管末端沿极化肌动蛋白电缆的转运

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摘要

Microtubules and actin filaments interact and cooperate in many processes in eukaryotic cells, but the functional implications of such interactions are not well understood. In the yeast Saccharomyces cerevisiae, both cytoplasmic microtubules and actin filaments are needed for spindle orientation. In addition, this process requires the type V myosin protein Myo2, the microtubule end–binding protein Bim1, and Kar9. Here, we show that fusing Bim1 to the tail of the Myo2 is sufficient to orient spindles in the absence of Kar9, suggesting that the role of Kar9 is to link Myo2 to Bim1. In addition, we show that Myo2 localizes to the plus ends of cytoplasmic microtubules, and that the rate of movement of these cytoplasmic microtubules to the bud neck depends on the intrinsic velocity of Myo2 along actin filaments. These results support a model for spindle orientation in which a Myo2–Kar9–Bim1 complex transports microtubule ends along polarized actin cables. We also present data suggesting that a similar process plays a role in orienting cytoplasmic microtubules in mating yeast cells.
机译:微管和肌动蛋白丝在真核细胞的许多过程中相互作用和协同作用,但这种相互作用的功能含义尚不清楚。在酵母酿酒酵母中,纺锤体定向都需要胞质微管和肌动蛋白丝。此外,该过程还需要V型肌球蛋白Myo2,微管末端结合蛋白Bim1和Kar9。在这里,我们显示在没有Kar9的情况下将Bim1融合到Myo2的尾部就足以定向纺锤体,这表明Kar9的作用是将Myo2链接到Bim1。此外,我们表明,Myo2定位于细胞质微管的正端,并且这些细胞质微管向芽颈的移动速度取决于Myo2沿肌动蛋白丝的内在速度。这些结果支持了主轴定向模型,其中Myo2–Kar9–Bim1复合物沿着极化肌动蛋白电缆运输微管末端。我们还提出了数据,表明相似的过程在交配酵母细胞中定向细胞质微管中起作用。

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