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Spindle pole body-anchored Kar3 drives the nucleus along microtubules from another nucleus in preparation for nuclear fusion during yeast karyogamy

机译:纺锤极体锚定的Kar3沿另一个小核的微管驱动核为酵母核配子过程中的核融合做准备

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摘要

Nuclear migration during yeast karyogamy, termed nuclear congression, is required to initiate nuclear fusion. Congression involves a specific regulation of the microtubule minus end-directed kinesin-14 motor Kar3 and a rearrangement of the cytoplasmic microtubule attachment sites at the spindle pole bodies (SPBs). However, how these elements interact to produce the forces necessary for nuclear migration is less clear. We used electron tomography, molecular genetics, quantitative imaging, and first principles modeling to investigate how cytoplasmic microtubules are organized during nuclear congression. We found that Kar3, with the help of its light chain, Cik1, is anchored during mating to the SPB component Spc72 that also serves as a nucleator and anchor for microtubules via their minus ends. Moreover, we show that no direct microtubule–microtubule interactions are required for nuclear migration. Instead, SPB-anchored Kar3 exerts the necessary pulling forces laterally on microtubules emanating from the SPB of the mating partner nucleus. Therefore, a twofold symmetrical application of the core principle that drives nuclear migration in higher cells is used in yeast to drive nuclei toward each other before nuclear fusion.
机译:启动核融合需要酵母核蛋白配体过程中的核迁移,称为核大会。国会涉及对微管减去末端导向的驱动蛋白14电机Kar3的特定调节,以及纺锤极体(SPB)上胞质微管附着位点的重排。但是,这些元素如何相互作用以产生核迁移所需的力量尚不清楚。我们使用电子断层扫描,分子遗传学,定量成像和第一原理建模来研究核大会期间如何组织细胞质微管。我们发现,Kar3在其轻链Cik1的帮助下,在与SPB组件Spc72交配时被锚固,该SPC72组件也通过其负端充当成核剂和微管的锚定物。此外,我们表明核迁移不需要直接的微管-微管相互作用。取而代之的是,锚定SPB的Kar3在交配伴侣核的SPB产生的微管上横向施加必要的拉力。因此,在核融合之前,酵母中使用了驱动高等细胞中核迁移的核心原理的双重对称应用,以驱动核彼此接近。

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