Wu Huan, Guo Jia, Zhou Ya-Ting, Gao Xiang-Dong
Department of Microbiology, College of Life Sciences, Wuhan University, Wuhan, China.
Department of Microbiology, College of Life Sciences, Wuhan University, Wuhan, China Hubei Provincial Cooperative Innovation Center of Industrial Fermentation, Wuhan, China
Eukaryot Cell. 2015 Mar;14(3):241-51. doi: 10.1128/EC.00268-14. Epub 2015 Jan 9.
The anillin-related protein Bud4 of Saccharomyces cerevisiae is required for axial bud site selection by linking the axial landmark to the septins, which localize at the mother bud neck. Recent studies indicate that Bud4 plays a role in septin organization during cytokinesis. Here we show that Bud4 is also involved in septin organization during bud growth prior to cytokinesis, as bud4Δ shs1Δ cells displayed an elongated bud morphology and defective septin organization at 18°C. Bud4 overexpression also affected septin organization during bud growth in shs1Δ cells at 30°C. Bud4 was previously thought to associate with the septins via its central region, while the C-terminal anillin-related region was not involved in septin association. Surprisingly, we found that the central region of Bud4 alone targets to the bud neck throughout the cell cycle, unlike full-length Bud4, which localizes to the bud neck only during G2/M phase. We identified the anillin-related region to be a second targeting domain that cooperates with the central region for proper septin association. In addition, the anillin-related region could largely mediate Bud4's function in septin organization during bud growth and bud site selection. We show that this region interacts with the C terminus of Bud3 and the two segments depend on each other for association with the septins. Moreover, like the bud4Δ mutant, the bud3Δ mutant genetically interacts with shs1Δ and cdc12-6 mutants in septin organization, suggesting that Bud4 and Bud3 may cooperate in septin organization during bud growth. These observations provide new insights into the interaction of Bud4 with the septins and Bud3.
酿酒酵母中与膜收缩蛋白相关的蛋白Bud4通过将轴向标记与定位于母芽颈部的隔膜蛋白相连,从而参与轴向芽位的选择。最近的研究表明,Bud4在胞质分裂期间的隔膜蛋白组织中发挥作用。在此我们表明,Bud4在胞质分裂前的芽生长过程中也参与隔膜蛋白组织,因为在18°C时,bud4Δ shs1Δ细胞呈现出细长的芽形态且隔膜蛋白组织存在缺陷。在30°C时,Bud4的过表达也影响了shs1Δ细胞芽生长期间的隔膜蛋白组织。此前认为Bud4通过其中心区域与隔膜蛋白相关联,而C端与膜收缩蛋白相关的区域不参与与隔膜蛋白的关联。令人惊讶的是,我们发现单独的Bud4中心区域在整个细胞周期中都靶向芽颈部,这与全长Bud4不同,全长Bud4仅在G2/M期定位于芽颈部。我们确定与膜收缩蛋白相关的区域是第二个靶向结构域,它与中心区域协同作用以实现隔膜蛋白的正确关联。此外,与膜收缩蛋白相关区域在很大程度上可以介导Bud4在芽生长和芽位选择期间在隔膜蛋白组织中的功能。我们表明该区域与Bud3的C端相互作用,并且这两个片段在与隔膜蛋白的关联中相互依赖。此外,与bud4Δ突变体一样,bud3Δ突变体在隔膜蛋白组织中与shs1Δ和cdc12 - 6突变体发生遗传相互作用,这表明Bud4和Bud3可能在芽生长期间的隔膜蛋白组织中协同作用。这些观察结果为Bud4与隔膜蛋白和Bud3的相互作用提供了新的见解。