Role of Dynamin in the Formation of Transport Vesicles from the Trans-Golgi Network

Author:

Jones Steven M.12,Howell Kathryn E.12,Henley John R.12,Cao Hong12,McNiven Mark A.12

Affiliation:

1. J. R. Henley, H. Cao, M. A. McNiven, Center for Basic Research in Digestive Diseases, Mayo Clinic and Foundation, Rochester, MN 55905, USA.

2. S. M. Jones, K. E. Howell, Department of Cellular & Structural Biology, University of Colorado School of Medicine, 4200 East 9th Avenue, Denver, CO 80262, USA.

Abstract

Dynamin guanosine triphosphatases support the scission of clathrin-coated vesicles from the plasmalemma during endocytosis. By fluorescence microscopy of cultured rat hepatocytes, a green fluorescent protein–dynamin II fusion protein localized with clathrin-coated vesicles at the Golgi complex. A cell-free assay was utilized to demonstrate the role of dynamin in vesicle formation at the trans-Golgi. Addition of peptide-specific anti-dynamin antibodies to the assay mixture inhibited both constitutive exocytic and clathrin-coated vesicle formation. Immunodepletion of dynamin proteins also inhibited vesicle formation, and budding efficiency was restored upon readdition of purified dynamin. These data suggest that dynamin participates in the formation of distinct transport vesicles from the trans-Golgi network.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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