A cisternal progression mode of intra-Golgi transport requires that Golgi resident proteins recycle by peri-Golgi vesicles, whereas the alternative model of vesicular transport predicts anterograde cargo proteins to be present in such vesicles. We have used quantitative immuno-EM on NRK cells to distinguish peri-Golgi vesicles from other vesicles in the Golgi region. We found significant levels of the Golgi resident enzyme mannosidase II and the transport machinery proteins giantin, KDEL-receptor, and rBet1 in coatomer protein I–coated cisternal rims and peri-Golgi vesicles. By contrast, when cells expressed vesicular stomatitis virus protein G this anterograde marker was largely absent from the peri-Golgi vesicles. These data suggest a role of peri-Golgi vesicles in recycling of Golgi residents, rather than an important role in anterograde transport.
Peri-Golgi vesicles contain retrograde but not anterograde proteins consistent with the cisternal progression model of intra-Golgi transport
R. Scheller's present address is Genentech, Inc., 1 DNA Way, South San Francisco, CA, 94080-4990.
Abbreviations used in this paper: COP, coatomer protein; ER, endoplasmic reticulum; GFP, green fluorescent protein; IEM, immuno-EM; KDELr, KDEL receptor; Man, mannosidase; VSV-G, vesicular stomatitis virus protein G; VTC, vesicular tubular cluster.
José A. Martínez-Menárguez, Rytis Prekeris, Viola M.J. Oorschot, Richard Scheller, Jan W. Slot, Hans J. Geuze, Judith Klumperman; Peri-Golgi vesicles contain retrograde but not anterograde proteins consistent with the cisternal progression model of intra-Golgi transport . J Cell Biol 24 December 2001; 155 (7): 1213–1224. doi: https://doi.org/10.1083/jcb.200108029
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