Mondésert G, Clarke D J, Reed S I
Scripps Research Institute, Department of Molecular Biology, La Jolla, California 92037, USA.
Genetics. 1997 Oct;147(2):421-34. doi: 10.1093/genetics/147.2.421.
The regulation of secretion polarity and cell surface growth during the cell cycle is critical for proper morphogenesis and viability of Saccharomyces cerevisiae. A shift from isotropic cell surface growth to polarized growth is necessary for bud emergence and a repolarization of secretion to the bud neck is necessary for cell separation. Although alterations in the actin cytoskeleton have been implicated in these changes in secretion polarity, clearly other cellular systems involved in secretion are likely to be targets of cell cycle regulation. To investigate mechanisms coupling cell cycle progression to changes in secretion polarity in parallel with and downstream of regulation of actin polarization, we implemented a screen for mutants defective specifically in polarized growth but with normal actin cytoskeleton structure. These mutants fell into three classes: those partially defective in N-glycosylation, those linked to specific defects in the exocyst, and a third class neither defective in glycosylation nor linked to the exocyst. These results raise the possibility that changes in N-linked glycosylation may be involved in a signal linking cell cycle progression and secretion polarity and that the exocyst may have regulatory functions in coupling the secretory machinery to the polarized actin cytoskeleton.
在细胞周期中,分泌极性和细胞表面生长的调控对于酿酒酵母的正常形态发生和生存能力至关重要。从各向同性细胞表面生长转变为极性生长对于芽的出现是必要的,而分泌重新极化至芽颈对于细胞分离是必要的。尽管肌动蛋白细胞骨架的改变与这些分泌极性变化有关,但显然参与分泌的其他细胞系统可能是细胞周期调控的靶点。为了研究在肌动蛋白极化调控的平行和下游将细胞周期进程与分泌极性变化相偶联的机制,我们实施了一项筛选,寻找在极性生长方面存在特异性缺陷但肌动蛋白细胞骨架结构正常的突变体。这些突变体分为三类:N-糖基化部分缺陷的突变体、与外泌体特定缺陷相关的突变体,以及第三类既无糖基化缺陷也与外泌体无关的突变体。这些结果增加了以下可能性:N-连接糖基化的变化可能参与了将细胞周期进程与分泌极性相联系的信号传递,并且外泌体在将分泌机制与极性肌动蛋白细胞骨架偶联方面可能具有调控功能。