Pizon V, Desjardins M, Bucci C, Parton R G, Zerial M
INSERM U-248, Faculté de Médecine Lariboisière-Saint Louis, Paris, France.
J Cell Sci. 1994 Jun;107 ( Pt 6):1661-70. doi: 10.1242/jcs.107.6.1661.
Among the small GTPases of the Ras family, Rap proteins exhibit the highest homology with p21Ras. The four Rap proteins so far identified constitute two subgroups, comprising the Rap1(A,B) and the Rap2(A,B) proteins. The intracellular location of Rap1A, Rap1B and Rap2A proteins was investigated in mammalian cells by confocal immunofluorescence microscopy. Using a specific anti-Rap1 affinity-purified antibody, both Rap1A and Rap1B proteins were localized to late endocytic compartments (late endosomes/lysosomes) in fibroblasts. The localization of the Rap1A and B proteins transiently overexpressed with the vaccinia T7 system was identical to that observed for endogenous Rap1 proteins. In contrast, epitope-tagged Rap2A protein colocalized with several markers of the Golgi complex, thus indicating that its site of function was distinct from that of Rap1A. In addition, morphological and subcellular fractionation studies provided evidence for the association of Rap1 proteins with phagosomes displaying biochemical features of late endocytic structures in J774 macrophages. Thus, the localization of Rap1A and Rap1B implicates their involvement in late endocytic/phagocytic processes.
在Ras家族的小GTP酶中,Rap蛋白与p21Ras具有最高的同源性。目前已鉴定出的四种Rap蛋白构成两个亚组,包括Rap1(A、B)和Rap2(A、B)蛋白。通过共聚焦免疫荧光显微镜在哺乳动物细胞中研究了Rap1A、Rap1B和Rap2A蛋白的细胞内定位。使用特异性抗Rap1亲和纯化抗体,Rap1A和Rap1B蛋白均定位于成纤维细胞的晚期内吞区室(晚期内体/溶酶体)。用痘苗T7系统瞬时过表达的Rap1A和B蛋白的定位与内源性Rap1蛋白的定位相同。相反,表位标记的Rap2A蛋白与高尔基体复合体的几种标记物共定位,因此表明其功能位点与Rap1A不同。此外,形态学和亚细胞分级分离研究为Rap1蛋白与在J774巨噬细胞中显示晚期内吞结构生化特征的吞噬体的关联提供了证据。因此,Rap1A和Rap1B的定位表明它们参与晚期内吞/吞噬过程。