The small Ras-like GTPase BUD-1 modulates conidial germination and hyphal growth guidance in the filamentous fungus Neurospora crassa

IF 2.4 3区 生物学 Q3 GENETICS & HEREDITY
Nallely Cano-Domínguez , Olga A. Callejas-Negrete , Luis L. Pérez-Mozqueda , Juan M. Martínez-Andrade , Diego L. Delgado-Álvarez , Ernestina Castro-Longoria
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Abstract

In filamentous fungi, the hypha orientation is essential for polarized growth and morphogenesis. The ability to re-orient tip growth in response to environmental cues is critical for the colony survival. Therefore, hyphal tip orientation and tip extension are distinct mechanisms that operate in parallel during filamentous growth. In yeast, the axial growth orientation requires a pathway regulated by Rsr1p/Bud1p, a Ras-like GTPase protein, which determines the axial budding pattern. However, in filamentous fungi the function of the Rsr1/Bud1p gene (krev-1 homolog) has not been completely characterized. In this work, we characterized the phenotype of a homokaryon mutant Bud1p orthologous in Neurospora crassa (△bud-1) and tagged BUD-1 with the green fluorescent protein (GFP) to determine its localization and cell dynamics under confocal microscopy. During spore germination BUD-1 was localized at specific points along the plasma membrane and during germ tube emergence it was located at the tip of the germ tubes. In mature hyphae BUD-1 continued to be located at the cell tip and was also present at sites of branch emergence and at the time of septum formation. The △bud-1 mutant showed a delayed germination, and the orientation of hyphae was somewhat disrupted. Also, the hypha diameter was reduced approximately 37 % with respect to the wild type. The lack of BUD-1 affected the Spitzenkörper (Spk) formation, trajectory, the localization of polarisome components BNI-1 and SPA-2, and the actin cytoskeleton polarization. The results presented here suggest that BUD-1 participates in the establishment of a new polarity axis. It may also mediate the delivery of secretory vesicles for the efficient construction of new plasma membrane and cell wall.

小的ras样GTPase BUD-1调节丝状真菌粗神经孢子菌的分生孢子萌发和菌丝生长
在丝状真菌中,菌丝方向对极化生长和形态发生至关重要。根据环境线索重新定向尖端生长的能力对群体生存至关重要。因此,在菌丝生长过程中,菌丝尖端取向和尖端延伸是并行运行的不同机制。在酵母中,轴向生长方向需要一条由Rsr1p/Bud1p调控的途径,Rsr1p/Bud1p是一种类似ras的GTPase蛋白,它决定了轴向出芽模式。然而,在丝状真菌中,Rsr1/Bud1p基因(krev-1同源基因)的功能尚未完全确定。本研究对粗神经孢子虫(Neurospora crassa)同源核体突变体Bud1p(△bud-1)进行表型鉴定,并用绿色荧光蛋白(GFP)标记bud-1,在共聚焦显微镜下确定其定位和细胞动力学。在孢子萌发过程中,BUD-1定位于沿质膜的特定点上,在胚管萌发过程中,它定位于胚管的尖端。在成熟菌丝中,BUD-1继续位于细胞尖端,也出现在分支出现的位置和隔膜形成的时候。△bud-1突变体萌发延迟,菌丝取向有所改变。与野生型相比,菌丝直径减少了约37%。BUD-1的缺乏影响了Spitzenkörper (Spk)的形成、轨迹、极化体成分BNI-1和SPA-2的定位以及肌动蛋白细胞骨架的极化。本研究结果表明,BUD-1参与了新的极性轴的建立。它也可能介导分泌囊泡的传递,从而有效地构建新的质膜和细胞壁。
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来源期刊
Fungal Genetics and Biology
Fungal Genetics and Biology 生物-遗传学
CiteScore
6.20
自引率
3.30%
发文量
66
审稿时长
85 days
期刊介绍: Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny. Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists. Research Areas include: • Biochemistry • Cytology • Developmental biology • Evolutionary biology • Genetics • Molecular biology • Phylogeny • Physiology.
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