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Signalling complexes associated with adenylyl cyclase II are assembled during their biosynthesis.
- Source :
-
Cellular signalling [Cell Signal] 2007 Mar; Vol. 19 (3), pp. 481-9. Date of Electronic Publication: 2006 Sep 18. - Publication Year :
- 2007
-
Abstract
- We have previously demonstrated that adenylyl cyclase II (ACII) interacts with beta2-adrenergic receptors and heterotrimeric G proteins as part of a pre-assembled signalling complex. In this study, we further show that AC interacts with these proteins before it is targetted to the cell surface. Using a combination of approaches including bioluminescence resonance energy transfer (BRET) in concert with subcellular fractionation, we show that ACII and beta2AR initially interact in the ER. Further, dominant-negative Rab1 and Sar1 GTPases which block anterograde trafficking out of the ER have no effect on either ACII/receptor or ACII/Gbetagamma protein interactions. However, DN Rab1 and Sar1 constructs (but not DN Rabs 2, 6, 8 or 11) prevent the inclusion of Galpha subunits in ACII signalling complexes suggesting it assembles into the complex at a slightly later stage. Thus, like Kir3.1 inwardly rectifying potassium channels, signalosomes containing ACII are formed during their biosynthesis and not in response to agonist at the cell surface.
- Subjects :
- Binding Sites
Cell Line
Endoplasmic Reticulum metabolism
Energy Transfer
Green Fluorescent Proteins metabolism
Humans
Luciferases metabolism
Luminescence
Microscopy, Fluorescence
Protein Binding
Receptors, Adrenergic, beta-2 metabolism
Subcellular Fractions
Adenylyl Cyclases metabolism
GTP-Binding Protein alpha Subunits, Gi-Go biosynthesis
GTP-Binding Protein beta Subunits biosynthesis
Heterotrimeric GTP-Binding Proteins biosynthesis
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 0898-6568
- Volume :
- 19
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Cellular signalling
- Publication Type :
- Academic Journal
- Accession number :
- 16979872
- Full Text :
- https://doi.org/10.1016/j.cellsig.2006.07.021