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The clathrin adaptor Gga2p is a phosphatidylinositol 4-phosphate effector at the Golgi exit.
- Source :
-
Molecular biology of the cell [Mol Biol Cell] 2008 May; Vol. 19 (5), pp. 1991-2002. Date of Electronic Publication: 2008 Feb 20. - Publication Year :
- 2008
-
Abstract
- Phosphatidylinositol 4-phosphate (PI(4)P) is a key regulator of membrane transport required for the formation of transport carriers from the trans-Golgi network (TGN). The molecular mechanisms of PI(4)P signaling in this process are still poorly understood. In a search for PI(4)P effector molecules, we performed a screen for synthetic lethals in a background of reduced PI(4)P and found the gene GGA2. Our analysis uncovered a PI(4)P-dependent recruitment of the clathrin adaptor Gga2p to the TGN during Golgi-to-endosome trafficking. Gga2p recruitment to liposomes is stimulated both by PI(4)P and the small GTPase Arf1p in its active conformation, implicating these two molecules in the recruitment of Gga2p to the TGN, which ultimately controls the formation of clathrin-coated vesicles. PI(4)P binding occurs through a phosphoinositide-binding signature within the N-terminal VHS domain of Gga2p resembling a motif found in other clathrin interacting proteins. These data provide an explanation for the TGN-specific membrane recruitment of Gga2p.
- Subjects :
- 1-Phosphatidylinositol 4-Kinase metabolism
ADP-Ribosylation Factors metabolism
Adaptor Proteins, Vesicular Transport chemistry
Amino Acid Sequence
Genome, Fungal genetics
Golgi Apparatus ultrastructure
Kinetics
Models, Molecular
Molecular Sequence Data
Mutation genetics
Phenotype
Protein Binding
Protein Structure, Tertiary
Protein Transport
Saccharomyces cerevisiae cytology
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae ultrastructure
Saccharomyces cerevisiae Proteins chemistry
Vacuoles metabolism
trans-Golgi Network metabolism
trans-Golgi Network ultrastructure
Adaptor Proteins, Vesicular Transport metabolism
Clathrin metabolism
Golgi Apparatus metabolism
Phosphatidylinositol Phosphates metabolism
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1939-4586
- Volume :
- 19
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Molecular biology of the cell
- Publication Type :
- Academic Journal
- Accession number :
- 18287542
- Full Text :
- https://doi.org/10.1091/mbc.E06-10-0937