Department of Microbiology, Center for Scientific Research and Higher Education of Ensenada (CICESE), Ensenada, Baja California, Mexico.
PLoS One. 2012;7(1):e30372. doi: 10.1371/journal.pone.0030372. Epub 2012 Jan 24.
A key multiprotein complex involved in regulating the actin cytoskeleton and secretory machinery required for polarized growth in fungi, is the polarisome. Recognized core constituents in budding yeast are the proteins Spa2, Pea2, Aip3/Bud6, and the key effector Bni1. Multicellular fungi display a more complex polarized morphogenesis than yeasts, suggesting that the filamentous fungal polarisome might fulfill additional functions. In this study, we compared the subcellular organization and dynamics of the putative polarisome components BUD-6 and BNI-1 with those of the bona fide polarisome marker SPA-2 at various developmental stages of Neurospora crassa. All three proteins exhibited a yeast-like polarisome configuration during polarized germ tube growth, cell fusion, septal pore plugging and tip repolarization. However, the localization patterns of all three proteins showed spatiotemporally distinct characteristics during the establishment of new polar axes, septum formation and cytokinesis, and maintained hyphal tip growth. Most notably, in vegetative hyphal tips BUD-6 accumulated as a subapical cloud excluded from the Spitzenkörper (Spk), whereas BNI-1 and SPA-2 partially colocalized with the Spk and the tip apex. Novel roles during septal plugging and cytokinesis, connected to the reinitiation of tip growth upon physical injury and conidial maturation, were identified for BUD-6 and BNI-1, respectively. Phenotypic analyses of gene deletion mutants revealed additional functions for BUD-6 and BNI-1 in cell fusion regulation, and the maintenance of Spk integrity. Considered together, our findings reveal novel polarisome-independent functions of BUD-6 and BNI-1 in Neurospora, but also suggest that all three proteins cooperate at plugged septal pores, and their complex arrangement within the apical dome of mature hypha might represent a novel aspect of filamentous fungal polarisome architecture.
参与调节真菌极性生长所需的肌动蛋白细胞骨架和分泌机制的关键多蛋白复合物是极化体。在出芽酵母中,公认的核心成分是 Spa2、Pea2、Aip3/Bud6 和关键效应因子 Bni1。与酵母相比,多细胞真菌表现出更复杂的极性形态发生,这表明丝状真菌的极化体可能具有额外的功能。在这项研究中,我们比较了假定的极化体成分 BUD-6 和 BNI-1 与真正的极化体标记 SPA-2 在粗糙脉孢菌不同发育阶段的亚细胞组织和动力学。在极性芽管生长、细胞融合、隔膜孔堵塞和尖端重极化过程中,这三种蛋白质都表现出类似酵母的极化体构型。然而,在新极轴的建立、隔膜形成和细胞分裂过程中,以及维持菌丝尖端生长过程中,所有三种蛋白质的定位模式都表现出时空上的显著特征。最值得注意的是,在营养菌丝的尖端,BUD-6 作为一个亚顶云积累,被排除在 Spitzenkörper(Spk)之外,而 BNI-1 和 SPA-2 部分与 Spk 和尖端顶点共定位。BUD-6 和 BNI-1 在隔膜堵塞和细胞分裂过程中分别鉴定出与物理损伤后尖端生长重新开始和分生孢子成熟相关的新作用。对基因缺失突变体的表型分析揭示了 BUD-6 和 BNI-1 在细胞融合调节以及 Spk 完整性维持中的额外功能。综合考虑,我们的研究结果揭示了 BUD-6 和 BNI-1 在粗糙脉孢菌中的极化体非依赖性新功能,但也表明这三种蛋白质在堵塞的隔膜孔中合作,它们在成熟菌丝顶端帽中的复杂排列可能代表丝状真菌极化体结构的一个新方面。