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The Rsr1/Bud1 GTPase Interacts with Itself and the Cdc42 GTPase during Bud-Site Selection and Polarity Establishment in Budding Yeast

机译:Rsr1 / Bud1 GTPase与自己和Cdc42 GTPase在芽站点的芽站点选择和极性建立过程中相互作用。

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摘要

Cell polarization occurs along a single axis that is generally determined in response to spatial cues. In budding yeast, the Rsr1 GTPase and its regulators direct the establishment of cell polarity at the proper cortical location in response to cell type–specific cues. Here we use a combination of in vivo and in vitro approaches to understand how Rsr1 polarization is established. We find that Rsr1 associates with itself in a spatially and temporally controlled manner. The homotypic interaction and localization of Rsr1 to the mother-bud neck and to the subsequent division site are dependent on its GDP-GTP exchange factor Bud5. Analyses of rsr1 mutants suggest that Bud5 recruits Rsr1 to these sites and promotes the homodimer formation. Rsr1 also exhibits heterotypic interaction with the Cdc42 GTPase in vivo. We show that the polybasic region of Rsr1 is necessary for the efficient homotypic and heterotypic interactions, selection of a proper growth site, and polarity establishment. Our findings thus suggest that dimerization of GTPases may be an efficient mechanism to set up cellular asymmetry.
机译:细胞极化沿着通常响应于空间线索而确定的单个轴发生。在发芽酵母中,Rsr1 GTPase及其调节剂可根据细胞类型特异性提示,在正确的皮质位置指导细胞极性的建立。在这里,我们结合使用体内和体外方法来了解如何建立Rsr1极化。我们发现Rsr1以时空受控的方式与其自身关联。 Rsr1的同型相互作用和定位在母芽颈和随后的分裂位点取决于其GDP-GTP交换因子Bud5。 rsr1突变体的分析表明,Bud5将Rsr1募集到这些位点并促进同型二聚体的形成。 Rsr1还表现出与Cdc42 GTPase在体内的异型相互作用。我们显示,Rsr1的多元区域对于有效的同型和异型相互作用,选择合适的生长位点和建立极性是必需的。因此,我们的发现表明,GTPases的二聚化可能是建立细胞不对称性的有效机制。

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