Morsomme Pierre, Prescianotto-Baschong Cristina, Riezman Howard
Biozentrum of the University of Basel, Basel, Switzerland.
J Cell Biol. 2003 Aug 4;162(3):403-12. doi: 10.1083/jcb.200212101. Epub 2003 Jul 28.
Glycosylphosphatidylinositol (GPI)-anchored proteins exit the ER in distinct vesicles from other secretory proteins, and this sorting event requires the Rab GTPase Ypt1p, tethering factors Uso1p, and the conserved oligomeric Golgi complex. Here we show that proper sorting depended on the vSNAREs, Bos1p, Bet1p, and Sec22p. However, the t-SNARE Sed5p was not required for protein sorting upon ER exit. Moreover, the sorting defect observed in vitro with bos1-1 extracts was also observed in vivo and was visualized by EM. Finally, transport and maturation of the GPI-anchored protein Gas1p was specifically affected in a bos1-1 mutant at semirestrictive temperature. Therefore, we propose that v-SNAREs are part of the cargo protein sorting machinery upon exit from the ER and that a correct sorting process is necessary for proper maturation of GPI-anchored proteins.
糖基磷脂酰肌醇(GPI)锚定蛋白通过与其他分泌蛋白不同的囊泡离开内质网(ER),这种分选事件需要Rab GTP酶Ypt1p、拴系因子Uso1p和保守的寡聚高尔基体复合体。我们在此表明,正确的分选依赖于v-SNARE蛋白Bos1p、Bet1p和Sec22p。然而,内质网输出时蛋白质分选并不需要t-SNARE蛋白Sed5p。此外,在体外bos1-1提取物中观察到的分选缺陷在体内也能观察到,并且通过电子显微镜(EM)得以显现。最后,在半限制温度下,bos1-1突变体中GPI锚定蛋白Gas1p的运输和成熟受到了特异性影响。因此,我们提出v-SNARE蛋白是内质网输出时货物蛋白分选机制的一部分,并且正确的分选过程对于GPI锚定蛋白的正常成熟是必要的。