Tall G G, Hama H, DeWald D B, Horazdovsky B F
Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75235-9038, USA.
Mol Biol Cell. 1999 Jun;10(6):1873-89. doi: 10.1091/mbc.10.6.1873.
Activated GTP-bound Rab proteins are thought to interact with effectors to elicit vesicle targeting and fusion events. Vesicle-associated v-SNARE and target membrane t-SNARE proteins are also involved in vesicular transport. Little is known about the functional relationship between Rabs and SNARE protein complexes. We have constructed an activated allele of VPS21, a yeast Rab protein involved in vacuolar protein sorting, and demonstrated an allele-specific interaction between Vps21p and Vac1p. Vac1p was found to bind the Sec1p homologue Vps45p. Although no association between Vps21p and Vps45p was seen, a genetic interaction between VPS21 and VPS45 was observed. Vac1p contains a zinc-binding FYVE finger that may bind phosphatidylinositol 3-phosphate [PtdIns(3)P]. In other FYVE domain proteins, this motif and PtdIns(3)P are necessary for membrane association. Vac1 proteins with mutant FYVE fingers still associated with membranes but showed vacuolar protein sorting defects and reduced interactions with Vps45p and activated Vps21p. Vac1p membrane association was not dependent on PtdIns(3)P, Pep12p, Vps21p, Vps45p, or the PtdIns 3-kinase, Vps34p. Vac1p FYVE finger mutant missorting phenotypes were suppressed by a defective allele of VPS34. These data indicate that PtdIns(3)P may perform a regulatory role, possibly involved in mediating Vac1p protein-protein interactions. We propose that activated-Vps21p interacts with its effector, Vac1p, which interacts with Vps45p to regulate the Golgi to endosome SNARE complex.
人们认为,结合GTP的活化Rab蛋白与效应器相互作用,引发囊泡靶向和融合事件。囊泡相关的v-SNARE蛋白和靶膜t-SNARE蛋白也参与囊泡运输。关于Rab蛋白与SNARE蛋白复合物之间的功能关系,人们了解甚少。我们构建了VPS21的一个活化等位基因,VPS21是一种参与液泡蛋白分选的酵母Rab蛋白,并证明了Vps21p与Vac1p之间存在等位基因特异性相互作用。发现Vac1p能结合Sec1p的同源物Vps45p。虽然未观察到Vps21p与Vps45p之间存在关联,但观察到VPS21与VPS45之间存在遗传相互作用。Vac1p含有一个可能结合磷脂酰肌醇3-磷酸[PtdIns(3)P]的锌结合FYVE结构域。在其他含FYVE结构域的蛋白中,该基序和PtdIns(3)P对于膜结合是必需的。具有突变FYVE结构域的Vac1蛋白仍与膜结合,但表现出液泡蛋白分选缺陷,并且与Vps45p和活化的Vps21p的相互作用减少。Vac1p的膜结合不依赖于PtdIns(3)P、Pep12p、Vps21p、Vps45p或磷脂酰肌醇3-激酶Vps34p。VPS34的一个缺陷等位基因抑制了Vac1p FYVE结构域突变体的错分选表型。这些数据表明,PtdIns(3)P可能发挥调节作用,可能参与介导Vac1p的蛋白质-蛋白质相互作用。我们提出,活化的Vps21p与其效应器Vac1p相互作用,Vac1p与Vps45p相互作用以调节高尔基体至内体的SNARE复合物。