Abstract
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.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Autoantigens / metabolism
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Cell Cycle / physiology*
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Cell Line
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Coat Protein Complex I
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Golgi Apparatus / physiology*
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Golgi Apparatus / ultrastructure
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Golgi Matrix Proteins
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Green Fluorescent Proteins
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Intracellular Membranes / metabolism
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Intracellular Membranes / ultrastructure
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Kidney
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Luminescent Proteins / genetics
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Luminescent Proteins / metabolism
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Membrane Glycoproteins*
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Membrane Proteins / metabolism
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Microscopy, Immunoelectron
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Protein Transport*
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Rats
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Receptors, Peptide / metabolism
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Recombinant Proteins / metabolism
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Transfection
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Vesicular stomatitis Indiana virus / physiology
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Viral Envelope Proteins / metabolism
Substances
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Autoantigens
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Coat Protein Complex I
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G protein, vesicular stomatitis virus
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Golgi Matrix Proteins
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KDEL receptor
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Luminescent Proteins
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Membrane Glycoproteins
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Membrane Proteins
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Receptors, Peptide
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Recombinant Proteins
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Viral Envelope Proteins
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macrogolgin
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Green Fluorescent Proteins