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The GAP Domain and the SNARE, Coatomer and Cargo Interaction Region of the ArfGAP2/3 Glo3 are Sufficient for Glo3 Function
Authors:Christina Schindler  Fernanda Rodriguez  Pak P. Poon  Richard A. Singer  Gerald C. Johnston   Anne Spang
Affiliation:Biozentrum, University of Basel, Klingelbergstrasse 70, CH-4056 Basel, Switzerland; Department of Microbiology &Immunology, Dalhousie University, Halifax, Nova Scotia, Canada B3H 1X5; Department of Biochemistry &Molecular Biology, Dalhousie University, Halifax, Nova Scotia, Canada B3H 1X5
Abstract:The ArfGAP Glo3 is required for coat protein I vesicle generation in the Golgi–endoplasmic reticulum (ER) shuttle. The best-understood role of Glo3 is the stimulation of the GTPase activity of Arf1. In this study, we characterized functional domains of the ArfGAP Glo3 and identified an interaction interface for coatomer, SNAREs and cargo in the central region of Glo3 (BoCCS region). The GAP domain together with the BoCCS region is necessary and sufficient for all vital Glo3 functions. Expression of a truncated Glo3 lacking the GAP domain results in a dominant negative growth phenotype in glo3 Δ cells at 37°C. This phenotype was alleviated by mutating either the BoCCS region or the Glo3 regulatory motif (GRM), or by overexpression of ER–Golgi SNAREs or the ArfGAP Gcs1. The GRM is not essential for Glo3 function; it may act as an intrinsic sensor coupling GAP activity to SNARE binding to avoid dead-end complex formation at the Golgi membrane. Our data suggest that membrane-interaction modules and cargo-sensing regions have evolved independently in ArfGAP1s versus ArfGAP2/3s.
Keywords:Arf1    ArfGAP    COPI    intracellular transport    small GTPases    vesicular transport    yeast
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