Kitagaki Hiroshi, Ito Kiyoshi, Shimoi Hitoshi
National Research Institute of Brewing, 3-7-1, Kagamiyama, Higashihiroshima, Hiroshima, Japan 739-0046.
Eukaryot Cell. 2004 Oct;3(5):1297-306. doi: 10.1128/EC.3.5.1297-1306.2004.
Dcw1p and Dfg5p in Saccharomyces cerevisiae are homologous proteins that were previously shown to be involved in cell wall biogenesis and to be essential for growth. Dcw1p was found to be a glycosylphosphatidylinositol-anchored membrane protein. To investigate the roles of these proteins in cell wall biogenesis and cell growth, we constructed mutant alleles of DCW1 by random mutagenesis, introduced them into a Deltadcw1 Deltadfg5 background, and isolated a temperature-sensitive mutant, DC61 (dcw1-3 Deltadfg5). When DC61 cells were incubated at 37 degrees C, most cells had small buds, with areas less than 20% of those of the mother cells. This result indicates that DC61 cells arrest growth with small buds at 37 degrees C. At 37 degrees C, fewer DC61 cells had 1N DNA content and most of them still had a single nucleus located apart from the bud neck. In addition, in DC61 cells incubated at 37 degrees C, bipolar spindles were not formed. These results indicate that DC61 cells, when incubated at 37 degrees C, are cell cycle arrested after DNA replication and prior to the separation of spindle pole bodies. The small buds of DC61 accumulated chitin in the bud cortex, and some of them were lysed, which indicates that they had aberrant cell walls. A temperature-sensitive dfg5 mutant, DF66 (Deltadcw1 dfg5-29), showed similar phenotypes. DCW1 and DFG5 mRNA levels peaked in the G1 and S phases, respectively. These results indicate that Dcw1p and Dfg5p are involved in bud formation through their involvement in biogenesis of the bud cell wall.
酿酒酵母中的Dcw1p和Dfg5p是同源蛋白,先前已证明它们参与细胞壁生物合成且对生长至关重要。发现Dcw1p是一种糖基磷脂酰肌醇锚定膜蛋白。为了研究这些蛋白在细胞壁生物合成和细胞生长中的作用,我们通过随机诱变构建了DCW1的突变等位基因,将它们导入Δdcw1Δdfg5背景中,并分离出一个温度敏感突变体DC61(dcw1-3Δdfg5)。当DC61细胞在37℃孵育时,大多数细胞有小芽,其面积小于母细胞的20%。这一结果表明DC61细胞在37℃时以小芽形式停止生长。在37℃时,较少的DC61细胞具有1N DNA含量,并且它们中的大多数仍然有一个位于芽颈之外的单核。此外,在37℃孵育的DC61细胞中,未形成双极纺锤体。这些结果表明,DC61细胞在37℃孵育时,在DNA复制后且在纺锤极体分离之前细胞周期停滞。DC61的小芽在芽皮层积累几丁质,并且其中一些被裂解,这表明它们具有异常的细胞壁。一个温度敏感的dfg5突变体DF66(Δdcw1 dfg5-29)表现出类似的表型。DCW1和DFG5 mRNA水平分别在G1期和S期达到峰值。这些结果表明Dcw1p和Dfg5p通过参与芽细胞壁的生物合成而参与芽的形成。