Pammer M, Briza P, Ellinger A, Schuster T, Stucka R, Feldmann H, Breitenbach M
Institut für Mikrobiologie und Genetik, Universität Wien, Austria.
Yeast. 1992 Dec;8(12):1089-99. doi: 10.1002/yea.320081211.
A mutant screen has been designed to isolate mutants in Saccharomyces cerevisiae deficient in spore wall dityrosine. As shown by electron microscopy, most of the mutant spores lacked only the outermost, dityrosine-rich layer of the spore wall. Mutant dit101, however, was additionally lacking the chitosan layer of the spore wall. Chemical measurements showed that this mutant does not synthesize chitosan during sporulation. The mutant spores were viable but sensitive to lytic enzymes (glusulase or zymolyase). Unlike most of the dit-mutants, dit101 did show a distinctive phenotype in vegetative cells: they grew normally but contained very little chitin and were therefore resistant to the toxic chitin-binding dye, Calcofluor White. The cells showed barely detectable staining of the walls with Calcofluor White or primulin. The decrease in the amount of chitin in vegetative cells and the absence of chitosan in spores suggested that the mutant dit101 could be defective in a chitin synthase. Indeed, a genomic yeast clone harboring the gene, CSD2, sharing significant sequence similarity with yeast chitin synthases I and II (C. E. Bulawa (1992), Mol. Cell. Biol. 12, 1764-1776), complemented our mutant and was shown to correspond to the chromosomal locus of dit101. Thus, the mutations dit101 and csd2 (and probably also call; M. H. Valdivieso et al., (1991), J. Cell Biol. 114, 101-109) were shown to be allelic. The gene was mapped to chromosome II and was located about 3 kb distal of GAL1. Using this DNA clone, a transcript of about 3500-4000 nucleotides was detected. Comparing RNA isolated from vegetative cells and from sporulating cells at different times throughout the sporulation process, no significant differences in DIT101 transcript levels could be detected indicating absence of sporulation-specific transcriptional regulation. However, the amount of DIT101 transcript changed significantly at different stages of the mitotic cell cycle, peaking after septum formation, but before cytokinesis. As most of the chitin synthesis of vegetative cells occurs at this stage of the cell division cycle, chitin synthesis mediated by DIT101 could be primarily regulated at the level of transcription in vegetatively growing cells.
已设计出一种突变体筛选方法,用于分离酿酒酵母中缺乏孢子壁二酪氨酸的突变体。电子显微镜观察显示,大多数突变体孢子仅缺少孢子壁最外层富含二酪氨酸的层。然而,突变体dit101还缺少孢子壁的壳聚糖层。化学分析表明,该突变体在孢子形成过程中不合成壳聚糖。突变体孢子是有活力的,但对裂解酶(葡糖淀粉酶或溶菌酶)敏感。与大多数dit突变体不同,dit101在营养细胞中确实表现出一种独特的表型:它们正常生长,但几丁质含量很少,因此对有毒的几丁质结合染料荧光增白剂具有抗性。用荧光增白剂或樱草灵对细胞壁染色,几乎检测不到细胞的染色。营养细胞中几丁质含量的减少以及孢子中壳聚糖的缺失表明,突变体dit101可能在一种几丁质合酶中存在缺陷。事实上,一个携带与酵母几丁质合酶I和II具有显著序列相似性的基因CSD2的基因组酵母克隆,对我们的突变体进行了互补,并被证明与dit101的染色体位点相对应。因此,dit101和csd2(可能还有call;M. H. Valdivieso等人,(1991年),《细胞生物学杂志》114卷,101 - 109页)的突变被证明是等位基因。该基因被定位到第二条染色体上,位于GAL1远端约3 kb处。利用这个DNA克隆,检测到一个约3500 - 4000个核苷酸的转录本。比较在整个孢子形成过程中不同时间从营养细胞和孢子形成细胞中分离的RNA,未检测到DIT101转录水平有显著差异,这表明不存在孢子形成特异性转录调控。然而,DIT101转录本的量在有丝分裂细胞周期的不同阶段有显著变化,在隔膜形成后但在胞质分裂前达到峰值。由于营养细胞的大多数几丁质合成发生在细胞分裂周期这个阶段,由DIT101介导的几丁质合成可能主要在营养生长细胞的转录水平上受到调控。