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Rsr1 Focuses Cdc42 Activity at Hyphal Tips and Promotes Maintenance of Hyphal Development in Candida albicans

机译:Rsr1集中Cdc42活动在菌丝尖端并促进白色念珠菌菌丝发育的维持。

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摘要

The extremely elongated morphology of fungal hyphae is dependent on the cell's ability to assemble and maintain polarized growth machinery over multiple cell cycles. The different morphologies of the fungus Candida albicans make it an excellent model organism in which to study the spatiotemporal requirements for constitutive polarized growth and the generation of different cell shapes. In C. albicans, deletion of the landmark protein Rsr1 causes defects in morphogenesis that are not predicted from study of the orthologous protein in the related yeast Saccharomyces cerevisiae, thus suggesting that Rsr1 has expanded functions during polarized growth in C. albicans. Here, we show that Rsr1 activity localizes to hyphal tips by the differential localization of the Rsr1 GTPase-activating protein (GAP), Bud2, and guanine nucleotide exchange factor (GEF), Bud5. In addition, we find that Rsr1 is needed to maintain the focused localization of hyphal polarity structures and proteins, including Bem1, a marker of the active GTP-bound form of the Rho GTPase, Cdc42. Further, our results indicate that tip-localized Cdc42 clusters are associated with the cell's ability to express a hyphal transcriptional program and that the ability to generate a focused Cdc42 cluster in early hyphae (germ tubes) is needed to maintain hyphal morphogenesis over time. We propose that in C. albicans, Rsr1 “fine-tunes” the distribution of Cdc42 activity and that self-organizing (Rsr1-independent) mechanisms of polarized growth are not sufficient to generate narrow cell shapes or to provide feedback to the transcriptional program during hyphal morphogenesis.
机译:真菌菌丝的极度伸长形态取决于细胞在多个细胞周期中组装和维持极化生长机制的能力。真菌白色念珠菌的不同形态使其成为研究自然组成型极化生长和不同细胞形状生成的时空需求的优秀模型生物。在白色念珠菌中,标志性蛋白Rsr1的缺失会导致形态发生缺陷,这是从相关酵母酿酒酵母的直系同源蛋白研究中无法预测的,因此表明Rsr1在白色念珠菌的极化生长过程中具有扩展的功能。在这里,我们显示Rsr1活性通过Rsr1 GTPase激活蛋白(GAP),Bud2和鸟嘌呤核苷酸交换因子(GEF),Bud5的差异化定位而定位于菌丝末端。此外,我们发现需要Rsr1来保持菌丝极性结构和蛋白质(包括Bem1)的集中定位,Bem1是Rho GTPase Cdc42的活性GTP结合形式的标志物。此外,我们的结果表明,尖端定位的Cdc42簇与细胞表达菌丝转录程序的能力有关,并且需要在早期菌丝(胚芽管)中生成聚焦的Cdc42簇的能力,以随着时间的推移保持菌丝形态的发生。我们建议在白色念珠菌中,Rsr1“微调” Cdc42活性的分布,并且极化生长的自组织(独立于Rsr1的)机制不足以产生狭窄的细胞形状或在转录过程中向转录程序提供反馈菌丝形态发生。

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