Hasek J, Rupes I, Svobodová J, Streiblová E
Institute of Microbiology, Czechoslovak Academy of Sciences, Prague.
J Gen Microbiol. 1987 Dec;133(12):3355-63. doi: 10.1099/00221287-133-12-3355.
The topology of tubulin and actin during mating of Saccharomyces cerevisiae was analysed by fluorescence microscopy with the monoclonal anti-tubulin antibody Tu01 and rhodamine-labelled phalloidin. Preconjugatory cells displayed an asymmetric distribution of the microtubule and actin cytoskeleton and an overall polarization of the cells preceding cell fusion. Prior to karyogamy, the haploid spindle pole bodies were associated with abundant cytoplasmic microtubules. Budding zygotes revealed the same tubulin and actin patterns as vegetative cells. Treatment of the mating mixture with the microtubule inhibitor nocodazole (10 micrograms ml-1) did not prevent polarization and fusion of haploids, zygote formation and emergence of the first zygotic bud. In marked contrast, the migration of the nucleus in preconjugatory cells as well as nuclear migration and fusion within the zygotes was unequivocally blocked by the action of the drug. It is suggested that the problem of the morphogenesis of mating should be approached by considering interactions at the cell periphery.
利用单克隆抗微管蛋白抗体Tu01和罗丹明标记的鬼笔环肽,通过荧光显微镜分析了酿酒酵母交配过程中微管蛋白和肌动蛋白的拓扑结构。接合前期细胞显示出微管和肌动蛋白细胞骨架的不对称分布以及细胞融合前细胞的整体极化。在核融合之前,单倍体纺锤体极体与丰富的细胞质微管相关。出芽的合子显示出与营养细胞相同的微管蛋白和肌动蛋白模式。用微管抑制剂诺考达唑(10微克/毫升)处理交配混合物并不能阻止单倍体的极化和融合、合子形成以及第一个合子芽的出现。与之形成鲜明对比的是,该药物的作用明确地阻断了接合前期细胞中的细胞核迁移以及合子内的核迁移和融合。研究表明,应通过考虑细胞周边的相互作用来解决交配形态发生的问题。