Kim H B, Haarer B K, Pringle J R
Department of Biology, University of Michigan, Ann Arbor 48109.
J Cell Biol. 1991 Feb;112(4):535-44. doi: 10.1083/jcb.112.4.535.
Budding cells of the yeast Saccharomyces cerevisiae possess a ring of 10-nm-diameter filaments, of unknown biochemical nature, that lies just inside the plasma membrane in the neck connecting the mother cell to its bud. Electron microscopic observations suggest that these filaments assemble at the budding site coincident with bud emergence and disassemble shortly before cytokinesis (Byers, B. and L. Goetsch. 1976. J. Cell Biol. 69:717-721). Mutants defective in any of four genes (CDC3, CDC10, CDC11, or CDC12) lack these filaments and display a pleiotropic phenotype that involves abnormal bud growth and an inability to complete cytokinesis. We showed previously by immunofluorescence that the CDC12 gene product is probably a constituent of the ring of 10-nm filaments (Haarer, B. and J. Pringle. 1987. Mol. Cell. Biol. 7:3678-3687). We now report the use of fusion proteins to generate polyclonal antibodies specific for the CDC3 gene product. In immunofluorescence experiments, these antibodies decorated the neck regions of wild-type and mutant cells in patterns suggesting that the CDC3 gene product is also a constituent of the ring of 10-nm filaments. We also used the CDC3-specific and CDC12-specific antibodies to investigate the timing of localization of these proteins to the budding site. The results suggest that the CDC3 protein is organized into a ring at the budding site well before bud emergence and remains so organized for some time after cytokinesis. The CDC12 product appears to behave similarly, but may arrive at the budding site closer to the time of bud emergence, and disappear from that site more quickly after cytokinesis, than does the CDC3 product. Examination of mating cells and cells responding to purified mating pheromone revealed novel arrangements of the CDC3 and CDC12 products in the regions of cell wall reorganization. Both proteins were present in normal-looking ring structures at the bases of the first zygotic buds.
酿酒酵母的出芽细胞在连接母细胞和芽的颈部质膜内侧有一圈直径为10纳米的丝状结构,其生化性质未知。电子显微镜观察表明,这些丝状结构在出芽位点随着芽的出现而组装,并在胞质分裂前不久解体(拜尔斯,B.和L.戈奇。1976年。《细胞生物学杂志》69:717 - 721)。四个基因(CDC3、CDC10、CDC11或CDC12)中任何一个有缺陷的突变体都缺乏这些丝状结构,并表现出多效性表型,包括异常的芽生长和无法完成胞质分裂。我们之前通过免疫荧光显示,CDC12基因产物可能是10纳米丝状环的一个组成部分(哈勒,B.和J.普林格尔。1987年。《分子细胞生物学》7:3678 - 3687)。我们现在报告利用融合蛋白产生针对CDC3基因产物的多克隆抗体。在免疫荧光实验中,这些抗体以特定模式标记野生型和突变体细胞的颈部区域,表明CDC3基因产物也是10纳米丝状环的一个组成部分。我们还使用CDC3特异性抗体和CDC12特异性抗体来研究这些蛋白质定位到出芽位点的时间。结果表明,CDC3蛋白在芽出现之前就已在出芽位点组装成环,并且在胞质分裂后一段时间内仍保持这种组装状态。CDC12产物的行为似乎类似,但可能比CDC3产物更接近芽出现的时间到达出芽位点,并且在胞质分裂后更快从该位点消失。对交配细胞和对纯化交配信息素作出反应的细胞的检查揭示了CDC3和CDC12产物在细胞壁重组区域的新排列方式。在第一个合子芽的基部,两种蛋白都存在于外观正常的环状结构中。