In situ Localization and in vitro Induction of Plant COPI-Coated Vesicles

Coat protein (COP)-coated vesicles have been shown to mediate protein transport through early steps of the secretory pathway in yeast and mammalian cells. Here, we attempt to elucidate their role in vesicular trafficking of plant cells, using a combined biochemical and ultrastructural approach. Immu...

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Bibliographic Details
Published in:The Plant cell 2000-11, Vol.12 (11), p.2219-2235
Main Authors: Pimpl, Peter, Movafeghi, Ali, Coughlan, Sean, Denecke, Jürgen, Hillmer, Stefan, Robinson, David G.
Format: Article
Language:English
Subjects:
Antibodies
Base Sequence
Brefeldin A - pharmacology
Capsid proteins
Cauliflower
Centrifugation
COP coated vesicles
Cross Reactions
Cytosol
DNA Primers
Endoplasmic Reticulum - metabolism
Freight
Golgi apparatus
Golgi Apparatus - metabolism
Immune Sera
Plant cells
Plant Proteins - antagonists & inhibitors
Plant Proteins - immunology
Plant Proteins - metabolism
Plants, Genetically Modified - metabolism
Protein Transport
Proteins
Transgenic plants
Yeasts
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Summary:Coat protein (COP)-coated vesicles have been shown to mediate protein transport through early steps of the secretory pathway in yeast and mammalian cells. Here, we attempt to elucidate their role in vesicular trafficking of plant cells, using a combined biochemical and ultrastructural approach. Immunogold labeling of cryosections revealed that COPI proteins are localized to microvesicles surrounding or budding from the Golgi apparatus. COPI-coated buds primarily reside on the cis-face of the Golgi stack. In addition, COPI and Arf1p show predominant labeling of the cis-Golgi stack, gradually diminishing toward the trans-Golgi stack. In vitro COPI-coated vesicle induction experiments demonstrated that Arf1p as well as coatomer could be recruited from cauliflower cytosol onto mixed endoplasmic reticulum (ER)/Golgi membranes. Binding of Arf1p and coatomer is inhibited by brefeldin A, underlining the specificity of the recruitment mechanism. In vitro vesicle budding was confirmed by identification of COPI-coated vesicles through immunogold negative staining in a fraction purified from isopycnic sucrose gradient centrifugation. Similar in vitro induction experiments with tobacco ER/Golgi membranes prepared from transgenic plants overproducing barley α-amylase-HDEL hielded a COPI-coated vesicle fraction that contained α-amylase as well as calreticulin.
ISSN:1040-4651
1532-298X
DOI:10.1105/tpc.12.11.2219