Shugrue C A, Kolen E R, Peters H, Czernik A, Kaiser C, Matovcik L, Hubbard A L, Gorelick F
Gastroenterology Section, Dept of Medicine, Yale University School of Medicine, New Haven, CT, USA.
J Cell Sci. 1999 Dec;112 ( Pt 24)(Pt 24):4547-56. doi: 10.1242/jcs.112.24.4547.
The regulation of intracellular vesicular trafficking is mediated by specific families of proteins that are involved in vesicular budding, translocation, and fusion with target membranes. We purified a vesicle-associated protein from hepatic microsomes using sequential column chromatography and partially sequenced it. Oliogonucleotides based on these sequences were used to clone the protein from a rat liver cDNA library. The clone encoded a novel protein with a predicted mass of 137 kDa (p137). The protein had an N terminus WD repeat motif with significant homology to Sec31p, a member of the yeast COPII coat that complexes with Sec13p. We found that p137 interacted with mammalian Sec13p using several approaches: co-elution through sequential column chromatography, co-immunoprecipitation from intact cells, and yeast two-hybrid analysis. Morphologically, the p137 protein was localized to small punctate structures in the cytoplasm of multiple cultured cell lines. When Sec13p was transfected into these cells, it demonstrated considerable overlap with p137. This overlap was maintained through several pharmacological manipulations. The p137 compartment also demonstrated partial overlap with ts045-VSVG protein when infected cells were incubated at 15 degrees C. These findings suggest that p137 is the mammalian orthologue of Sec31p.
细胞内囊泡运输的调控由特定的蛋白质家族介导,这些蛋白质参与囊泡的出芽、转运以及与靶膜的融合。我们利用连续柱层析从肝微粒体中纯化了一种囊泡相关蛋白,并对其进行了部分测序。基于这些序列的寡核苷酸被用于从大鼠肝脏cDNA文库中克隆该蛋白。该克隆编码一种预测分子量为137 kDa的新型蛋白(p137)。该蛋白的N端具有WD重复基序,与Sec31p具有显著同源性,Sec31p是酵母COPII衣被的成员,可与Sec13p形成复合物。我们通过几种方法发现p137与哺乳动物的Sec13p相互作用:通过连续柱层析共洗脱、从完整细胞中共免疫沉淀以及酵母双杂交分析。在形态学上,p137蛋白定位于多种培养细胞系细胞质中的小斑点状结构。当将Sec13p转染到这些细胞中时,它与p137表现出相当大的重叠。通过几种药理学操作,这种重叠得以维持。当感染的细胞在15℃孵育时,p137区室也与ts045-VSVG蛋白表现出部分重叠。这些发现表明p137是Sec31p的哺乳动物同源物。