Ni L, Snyder M
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA.
Mol Biol Cell. 2001 Jul;12(7):2147-70. doi: 10.1091/mbc.12.7.2147.
A genome-wide screen of 4168 homozygous diploid yeast deletion strains has been performed to identify nonessential genes that participate in the bipolar budding pattern. By examining bud scar patterns representing the sites of previous cell divisions, 127 mutants representing three different phenotypes were found: unipolar, axial-like, and random. From this screen, 11 functional classes of known genes were identified, including those involved in actin-cytoskeleton organization, general bud site selection, cell polarity, vesicular transport, cell wall synthesis, protein modification, transcription, nuclear function, translation, and other functions. Four characterized genes that were not known previously to participate in bud site selection were also found to be important for the haploid axial budding pattern. In addition to known genes, we found 22 novel genes (20 are designated BUD13-BUD32) important for bud site selection. Deletion of one resulted in unipolar budding exclusively from the proximal pole, suggesting that this gene plays an important role in diploid distal budding. Mutations in 20 other novel BUD genes produced a random budding phenotype and one produced an axial-like budding defect. Several of the novel Bud proteins were fused to green fluorescence protein; two proteins were found to localize to sites of polarized cell growth (i.e., the bud tip in small budded cells and the neck in cells undergoing cytokinesis), similar to that postulated for the bipolar signals and proteins that target cell division site tags to their proper location in the cell. Four others localized to the nucleus, suggesting that they play a role in gene expression. The bipolar distal marker Bud8 was localized in a number of mutants; many showed an altered Bud8-green fluorescence protein localization pattern. Through the genome-wide identification and analysis of different mutants involved in bipolar bud site selection, an integrated pathway for this process is presented in which proximal and distal bud site selection tags are synthesized and localized at their appropriate poles, thereby directing growth at those sites. Genome-wide screens of defined collections of mutants hold significant promise for dissecting many biological processes in yeast.
对4168个纯合二倍体酵母缺失菌株进行了全基因组筛选,以鉴定参与双极出芽模式的非必需基因。通过检查代表先前细胞分裂位点的芽痕模式,发现了代表三种不同表型的127个突变体:单极、轴样和随机。从该筛选中,鉴定出11个已知基因的功能类别,包括那些参与肌动蛋白细胞骨架组织、一般芽位选择、细胞极性、囊泡运输、细胞壁合成、蛋白质修饰、转录、核功能、翻译和其他功能的基因。还发现了四个先前未知参与芽位选择的特征基因对单倍体轴出芽模式也很重要。除了已知基因外,我们还发现了22个对芽位选择很重要的新基因(20个被命名为BUD13 - BUD32)。缺失其中一个基因导致仅从近端极进行单极出芽,这表明该基因在二倍体远端出芽中起重要作用。其他20个新的BUD基因的突变产生了随机出芽表型,一个产生了轴样出芽缺陷。几个新的Bud蛋白与绿色荧光蛋白融合;发现两种蛋白定位于极化细胞生长的位点(即小芽细胞中的芽尖和进行胞质分裂的细胞中的颈部),类似于双极信号和将细胞分裂位点标签靶向到细胞中适当位置的蛋白的推测定位。另外四个定位于细胞核,表明它们在基因表达中起作用。双极远端标记Bud8在许多突变体中定位;许多显示出Bud8 - 绿色荧光蛋白定位模式改变。通过对参与双极芽位选择的不同突变体进行全基因组鉴定和分析,提出了该过程的综合途径,其中近端和远端芽位选择标签在其适当的极合成并定位,从而指导这些位点的生长。对定义的突变体集合进行全基因组筛选对于剖析酵母中的许多生物学过程具有重要前景。