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GAP1(IP4BP)/RASA3 mediates Galphai-induced inhibition of mitogen-activated protein kinase.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2008 Dec 19; Vol. 283 (51), pp. 35908-17. Date of Electronic Publication: 2008 Oct 24. - Publication Year :
- 2008
-
Abstract
- The dopamine D2S receptor (short isoform) couples to inhibitory Galphai/o proteins to inhibit thyrotropin-releasing hormone (TRH)-stimulated p42/p44 mitogen-activated protein kinase (ERK1/2) phosphorylation in GH4ZR7 rat pituitary cells, consistent with its actions to inhibit prolactin gene transcription and cell proliferation. However, the underlying mechanism is unclear. To identify novel Galphai effectors, yeast two-hybrid screening of a GH4ZR7 cDNA library was done using constitutively active Galphai3-Q204L, and multiple clones of the RasGAP cDNA GAP1(IP4BP)/RASA3 were identified. In yeast mating assay, RASA3 preferentially interacted with activated forms of Galphai/o/z proteins, but not with Galphas. A direct interaction was indicated by in vitro pull-down assay, in which S-His-RASA3 preferentially bound guanosine 5'-O-(gamma-thio)triphosphate-activated Galphai3 and Galphai2 compared with guanosine 5'-O-(beta-thio)diphosphate-inactivated proteins. Similarly, in co-immunoprecipitation studies in HEK-293 cells, FLAG-tagged RASA3 preferentially interacted with activated mutants of Galphai3 and Galphai2 compared with wild type proteins. In GH4ZR7 cells, co-immunoprecipitation studies of endogenous proteins demonstrated a Galphai3-RASA3 complex that was induced upon TRH/D2S receptor co-activation. To address RASA3 function in dopamine D2S receptor-induced inhibition of ERK1/2 activity, endogenous RASA3 protein expression was suppressed (70% knockdown) in GH4ZR7 cells stably transfected with full-length antisense cDNA of RASA3. The selected antisense clones had similar levels of dopamine D2S receptor binding and D2S-induced inhibition of cAMP formation compared with parental GH4ZR7 cells. In these clones, D2S-mediated inhibition of TRH-induced phospho-ERK1/2 was reversed by 70-80% compared with parental GH4ZR7 cells. Our results provide a novel mechanism for dopamine D2S-induced inhibition of ERK1/2 and indicate that RASA3 links Galphai proteins to inhibit Gq-induced Ras/ERK1/2 activation.
- Subjects :
- Animals
Cell Line
DNA, Antisense genetics
DNA, Antisense metabolism
Dopamine D2 Receptor Antagonists
Enzyme Activation drug effects
Enzyme Activation physiology
GTP-Binding Protein alpha Subunits, Gi-Go genetics
Humans
Mice
Mitogen-Activated Protein Kinase 1 genetics
Mitogen-Activated Protein Kinase 3 genetics
Mitogens metabolism
Mitogens pharmacology
Protein Binding drug effects
Protein Binding physiology
Rats
Receptors, Cytoplasmic and Nuclear antagonists & inhibitors
Receptors, Cytoplasmic and Nuclear genetics
Receptors, Dopamine D2 genetics
Thyrotropin-Releasing Hormone genetics
Thyrotropin-Releasing Hormone metabolism
GTP-Binding Protein alpha Subunits, Gi-Go metabolism
Mitogen-Activated Protein Kinase 1 metabolism
Mitogen-Activated Protein Kinase 3 metabolism
Receptors, Cytoplasmic and Nuclear metabolism
Receptors, Dopamine D2 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 283
- Issue :
- 51
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 18952607
- Full Text :
- https://doi.org/10.1074/jbc.M803622200