Leaf D S, Blum L D
Department of Biology, Western Washington University, Bellingham, Washington, 98225, USA.
Exp Cell Res. 1998 Aug 25;243(1):39-49. doi: 10.1006/excr.1997.3917.
Rabs are a subfamily of ras-like GTPases required for membrane traffic in eukaryotic cells. In this report we describe the analysis of a rab10 GTPase expressed during sea urchin development. Protein distance measurements suggest that rab10 is less evolutionarily conserved than rabs 1, 2, and 3, particularly in the hypervariable C-terminus responsible for membrane targeting. Immunoblots and immunofluorescent stainings show that rab10 protein (rab10p) is expressed during all stages of sea urchin early development and in all embryonic cell types. Iterative deconvolutions of immunofluorescently stained embryos reveal that rab10p is localized to an extensive tubular network. Rab10p is not exclusively localized to the endoplasmic reticulum, as identified by anti-calsequestrin immunofluorescence. Double-labeling experiments with anti-rab10 antisera and wheat germ agglutinin, a trans-Golgi and trans-Golgi network (TGN) marker, demonstrate that rab10p is not localized to the trans-Golgi/TGN. Three-dimensional reconstructions of immunofluorescently labeled sea urchin embryonic cells show that tubules with greater concentrations of rab10p are closely apposed to trans-Golgi/TGN in a cis orientation-suggesting localization of rab10p to the cis-Golgi network. In mammalian cell lines, Rab10 has been localized to the trans-Golgi/trans-Golgi network (Y.-T. Chen et al., 1993, Proc. Natl. Acad. Sci. USA 90, 6508-6512). The localization of rab10 may not have been evolutionarily conserved between echinoderms and mammals because of the high rate of change in the hypervariable domain.
Rabs是真核细胞中膜运输所需的一类类Ras GTP酶亚家族。在本报告中,我们描述了对海胆发育过程中表达的一种rab10 GTP酶的分析。蛋白质距离测量表明,rab10在进化上的保守性低于rab1、rab2和rab3,特别是在负责膜靶向的高变C末端。免疫印迹和免疫荧光染色显示,rab10蛋白(rab10p)在海胆早期发育的所有阶段以及所有胚胎细胞类型中均有表达。对免疫荧光染色胚胎的迭代去卷积显示,rab10p定位于广泛的管状网络。通过抗钙网蛋白免疫荧光鉴定,rab10p并非仅定位于内质网。用抗rab10抗血清和小麦胚凝集素(一种反式高尔基体和反式高尔基体网络(TGN)标记物)进行的双标记实验表明,rab10p不定位于反式高尔基体/TGN。对免疫荧光标记的海胆胚胎细胞进行的三维重建显示,rab10p浓度较高的小管以顺式方向与反式高尔基体/TGN紧密相邻,这表明rab10p定位于顺式高尔基体网络。在哺乳动物细胞系中,Rab10已被定位于反式高尔基体/反式高尔基体网络(陈Y.-T.等人,1993年,《美国国家科学院院刊》90,6508-6512)。由于高变域变化率高,rab10的定位在棘皮动物和哺乳动物之间可能未在进化上保守。