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Regulation of light-dependent Gqalpha translocation and morphological changes in fly photoreceptors.
- Source :
-
The EMBO journal [EMBO J] 2003 Feb 03; Vol. 22 (3), pp. 459-68. - Publication Year :
- 2003
-
Abstract
- Heterotrimeric G-proteins relay signals between membrane-bound receptors and downstream effectors. Little is known, however, about the regulation of Galpha subunit localization within the natural endogenous environment of a specialized signaling cell. Here we show, using live Drosophila flies, that light causes massive and reversible translocation of the visual Gqalpha to the cytosol, associated with marked architectural changes in the signaling compartment. Molecular genetic dissection together with detailed kinetic analysis enabled us to characterize the translocation cycle and to unravel how signaling molecules that interact with Gqalpha affect these processes. Epistatic analysis showed that Gqalpha is necessary but not sufficient to bring about the morphological changes in the signaling organelle. Furthermore, mutant analysis indicated that Gqbeta is essential for targeting of Gqalpha to the membrane and suggested that Gqbeta is also needed for efficient activation of Gqalpha by rhodopsin. Our results support the 'two-signal model' hypothesis for membrane targeting in a living organism and characterize the regulation of both the activity-dependent Gq localization and the cellular architectural changes in Drosophila photoreceptors.
- Subjects :
- Actins metabolism
Animals
Cytoplasm chemistry
Cytoplasm metabolism
Dark Adaptation
Drosophila melanogaster ultrastructure
GTP-Binding Protein alpha Subunits, Gq-G11
Heterotrimeric GTP-Binding Proteins chemistry
Microfilament Proteins genetics
Microfilament Proteins metabolism
Models, Molecular
Organisms, Genetically Modified
Photoreceptor Cells, Invertebrate metabolism
Recombinant Fusion Proteins metabolism
Rhodopsin metabolism
Signal Transduction physiology
Drosophila melanogaster metabolism
Heterotrimeric GTP-Binding Proteins metabolism
Light
Photoreceptor Cells, Invertebrate ultrastructure
Protein Subunits metabolism
Protein Transport physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0261-4189
- Volume :
- 22
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- The EMBO journal
- Publication Type :
- Academic Journal
- Accession number :
- 12554647
- Full Text :
- https://doi.org/10.1093/emboj/cdg054