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Stable Preanaphase Spindle Positioning Requires Bud6p and an Apparent Interaction between the Spindle Pole Bodies and the Neck

机译:稳定的相位前主轴定位需要Bud6p并且主轴极体和颈部之间存在明显的相互作用

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摘要

Faithful partitioning of genetic material during cell division requires accurate spatial and temporal positioning of nuclei within dividing cells. In Saccharomyces cerevisiae, nuclear positioning is regulated by an elegant interplay between components of the actin and microtubule cytoskeletons. Regulators of this process include Bud6p (also referred to as the actin-interacting protein Aip3p) and Kar9p, which function to promote contacts between cytoplasmic microtubule ends and actin-delimited cortical attachment points. Here, we present the previously undetected association of Bud6p with the cytoplasmic face of yeast spindle pole bodies, the functional equivalent of metazoan centrosomes. Cells lacking Bud6p show exaggerated movements of the nucleus between mother and daughter cells and display reduced amounts of time a given spindle pole body spends in close association with the neck region of budding cells. Furthermore, overexpression of BUD6 greatly enhances interactions between the spindle pole body and mother-bud neck in a spindle alignment-defective dynactin mutant. These results suggest that association of either spindle pole body with neck components, rather than simply entry of a spindle pole body into the daughter cell, provides a positive signal for the progression of mitosis. We propose that Bud6p, through its localization at both spindle pole bodies and at the mother-bud neck, supports this positive signal and provides a regulatory mechanism to prevent excessive oscillations of preanaphase nuclei, thus reducing the likelihood of mitotic delays and nuclear missegregation.
机译:在细胞分裂过程中对遗传物质进行忠实的分配需要在分裂的细胞内准确地进行核的空间和时间定位。在酿酒酵母中,核位置由肌动蛋白和微管细胞骨架之间的相互作用来调节。该过程的调节剂包括Bud6p(也称为肌动蛋白相互作用蛋白Aip3p)和Kar9p,其功能是促进细胞质微管末端与肌动蛋白定界的皮质附着点之间的接触。在这里,我们介绍了Bud6p与酵母纺锤体极体(后生动物中心体的功能等同物)的胞质面先前未发现的关联。缺乏Bud6p的细胞在母细胞和子细胞之间显示出过大的核运动,并减少了给定纺锤体与芽出细胞的颈部密切相关的时间。此外,BUD6的过表达极大地增强了纺锤体定向缺陷的dactactin突变体中纺锤体和体芽之间的相互作用。这些结果表明,任一纺锤极体与颈部成分的结合,而不是简单地使纺锤极体进入子细胞,都为有丝分裂的发展提供了积极的信号。我们建议Bud6p通过定位在纺锤极体和母芽颈处来支持该阳性信号,并提供一种调节机制来防止前期核的过度振荡,从而降低有丝分裂延迟和核错聚的可能性。

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