Erdman S, Lin L, Malczynski M, Snyder M
Department of Biology, Yale University, New Haven, Connecticut 06520-8103, USA.
J Cell Biol. 1998 Feb 9;140(3):461-83. doi: 10.1083/jcb.140.3.461.
Yeast cells mate by an inducible pathway that involves agglutination, mating projection formation, cell fusion, and nuclear fusion. To obtain insight into the mating differentiation of Saccharomyces cerevisiae, we carried out a large-scale transposon tagging screen to identify genes whose expression is regulated by mating pheromone. 91,200 transformants containing random lacZ insertions were screened for beta-galactosidase (beta-gal) expression in the presence and absence of alpha factor, and 189 strains containing pheromone-regulated lacZ insertions were identified. Transposon insertion alleles corresponding to 20 genes that are novel or had not previously been known to be pheromone regulated were examined for effects on the mating process. Mutations in four novel genes, FIG1, FIG2, KAR5/ FIG3, and FIG4 were found to cause mating defects. Three of the proteins encoded by these genes, Fig1p, Fig2p, and Fig4p, are dispensible for cell polarization in uniform concentrations of mating pheromone, but are required for normal cell polarization in mating mixtures, conditions that involve cell-cell communication. Fig1p and Fig2p are also important for cell fusion and conjugation bridge shape, respectively. The fourth protein, Kar5p/Fig3p, is required for nuclear fusion. Fig1p and Fig2p are likely to act at the cell surface as Fig1:: beta-gal and Fig2::beta-gal fusion proteins localize to the periphery of mating cells. Fig4p is a member of a family of eukaryotic proteins that contain a domain homologous to the yeast Sac1p. Our results indicate that a variety of novel genes are expressed specifically during mating differentiation to mediate proper cell morphogenesis, cell fusion, and other steps of the mating process.
酵母细胞通过一种诱导途径进行交配,该途径涉及凝集、交配突起形成、细胞融合和核融合。为深入了解酿酒酵母的交配分化过程,我们进行了大规模转座子标签筛选,以鉴定其表达受交配信息素调控的基因。对91,200个含有随机lacZ插入片段的转化子在有无α因子存在的情况下进行β-半乳糖苷酶(β-gal)表达筛选,鉴定出189个含有受信息素调控的lacZ插入片段的菌株。检查了与20个新基因或先前未知受信息素调控的基因相对应的转座子插入等位基因对交配过程的影响。发现四个新基因FIG1、FIG2、KAR5/FIG3和FIG4中的突变会导致交配缺陷。这些基因编码的三种蛋白质,即Fig1p、Fig2p和Fig4p,在均匀浓度的交配信息素中对细胞极化并非必需,但在涉及细胞间通讯的交配混合物中进行正常细胞极化时是必需的。Fig1p和Fig2p分别对细胞融合和接合桥形状也很重要。第四种蛋白质Kar5p/Fig3p是核融合所必需的。Fig1p和Fig2p可能在细胞表面起作用,因为Fig1::β-gal和Fig2::β-gal融合蛋白定位于交配细胞的周边。Fig4p是真核蛋白质家族的成员,该家族包含与酵母Sac1p同源的结构域。我们的结果表明,多种新基因在交配分化过程中特异性表达,以介导适当的细胞形态发生、细胞融合和交配过程的其他步骤。