Heese-Peck Antje, Pichler Harald, Zanolari Bettina, Watanabe Reika, Daum Günther, Riezman Howard
Biozentrum, University of Basel, Switzerland.
Mol Biol Cell. 2002 Aug;13(8):2664-80. doi: 10.1091/mbc.e02-04-0186.
Sterols are essential factors for endocytosis in animals and yeast. To investigate the sterol structural requirements for yeast endocytosis, we created a variety of ergDelta mutants, each accumulating a distinct set of sterols different from ergosterol. Mutant erg2Deltaerg6Delta and erg3Deltaerg6Delta cells exhibit a strong internalization defect of the alpha-factor receptor (Ste2p). Specific sterol structures are necessary for pheromone-dependent receptor hyperphosphorylation, a prerequisite for internalization. The lack of phosphorylation is not due to a defect in Ste2p localization or in ligand-receptor interaction. Contrary to most known endocytic factors, sterols seem to function in internalization independently of actin. Furthermore, sterol structures are required at a postinternalization step of endocytosis. ergDelta cells were able to take up the membrane marker FM4-64, but exhibited defects in FM4-64 movement through endosomal compartments to the vacuole. Therefore, there are at least two roles for sterols in endocytosis. Based on sterol analysis, the sterol structural requirements for these two processes were different, suggesting that sterols may have distinct functions at different places in the endocytic pathway. Interestingly, sterol structures unable to support endocytosis allowed transport of the glycosylphosphatidylinositol-anchored protein Gas1p from the endoplasmic reticulum to Golgi compartment.
甾醇是动物和酵母中内吞作用的必需因子。为了研究酵母内吞作用对甾醇结构的要求,我们构建了多种ergDelta突变体,每个突变体积累一组与麦角固醇不同的独特甾醇。突变体erg2Deltaerg6Delta和erg3Deltaerg6Delta细胞表现出α因子受体(Ste2p)的强烈内化缺陷。特定的甾醇结构对于信息素依赖性受体的过度磷酸化是必需的,而过度磷酸化是内化的前提条件。磷酸化的缺乏并非由于Ste2p定位或配体-受体相互作用存在缺陷。与大多数已知的内吞因子相反,甾醇似乎在不依赖肌动蛋白的内化过程中发挥作用。此外,在内吞作用的内化后步骤需要甾醇结构。ergDelta细胞能够摄取膜标记物FM4-64,但在FM4-64通过内体区室转运至液泡的过程中表现出缺陷。因此,甾醇在内吞作用中至少有两个作用。基于甾醇分析,这两个过程对甾醇结构的要求不同,这表明甾醇可能在内吞途径的不同位置具有不同的功能。有趣的是,无法支持内吞作用的甾醇结构允许糖基磷脂酰肌醇锚定蛋白Gas1p从内质网转运至高尔基体区室。