Mondésert G, Reed S I
Department of Molecular Biology, Scripps Research Institute, La Jolla, California 92037, USA.
J Cell Biol. 1996 Jan;132(1-2):137-51. doi: 10.1083/jcb.132.1.137.
The ellipsoidal shape of the yeast Saccharomyces cerevisiae is the result of successive isotropic/apical growth switches that are regulated in a cell cycle-dependent manner. It is thought that growth polarity is governed by the remodeling of the actin cytoskeleton that is itself under the control of the cell cycle machinery. The cell cycle and the morphogenesis cycle are tightly coupled and it has been recently suggested that a morphogenesis/polarity checkpoint control monitors bud emergence in order to maintain the coupling of these two events (Lew, D. J., and S. I. Reed. 1995. J. Cell Biol. 129:739-749). During a screen based on the inability of cells impaired in the budding process to survive when the morphogenesis checkpoint control is abolished, we identified and characterized BED1, a new gene that is required for efficient budding. Cells carrying a disrupted allele of BED1 no longer have the wild-type ellipsoidal shape characteristic of S. cerevisiae, are larger than wild-type cells, are deficient in bud emergence, and depend upon an intact morphogenesis checkpoint control to survive. These cells show defects in polarized growth despite the fact that the actin cytoskeleton appears normal. Our results suggest that Bed1 is a type II membrane protein localized in the endoplasmic reticulum. BED1 is significantly homologous to gma12+, a S. pombe gene coding for an alpha-1,2,-galactosyltransferase, suggesting that glycosylation of specific proteins or lipids could be important for signaling in the switch to polarized growth and in bud emergence.
酿酒酵母的椭球形是由连续的各向同性/顶端生长转换导致的,这些转换以细胞周期依赖性方式受到调控。据认为,生长极性受肌动蛋白细胞骨架重塑的支配,而肌动蛋白细胞骨架本身受细胞周期机制的控制。细胞周期和形态发生周期紧密耦合,最近有人提出,一种形态发生/极性检查点控制会监测芽的出现,以维持这两个事件的耦合(Lew, D. J., 和 S. I. Reed. 1995. J. Cell Biol. 129:739 - 749)。在一项基于当形态发生检查点控制被废除时,出芽过程受损的细胞无法存活的筛选中,我们鉴定并表征了BED1,一个高效出芽所需的新基因。携带BED1中断等位基因的细胞不再具有酿酒酵母典型的野生型椭球形,比野生型细胞大,出芽不足,并且依赖完整的形态发生检查点控制来存活。尽管肌动蛋白细胞骨架看起来正常,但这些细胞在极性生长方面表现出缺陷。我们的结果表明,Bed1是一种定位于内质网的II型膜蛋白。BED1与gma12 +显著同源,gma12 +是粟酒裂殖酵母中一个编码α-1,2-半乳糖基转移酶的基因,这表明特定蛋白质或脂质的糖基化对于向极性生长转换和芽出现过程中的信号传导可能很重要。