Abstract
Drosophila genome encodes six alpha-subunits of heterotrimeric G proteins. The Gαs alpha-subunit is involved in the post-eclosion wing maturation, which consists of the epithelial-mesenchymal transition and cell death, accompanied by unfolding of the pupal wing into the firm adult flight organ. Here we show that another alpha-subunit Gαo can specifically antagonize the Gαs activities by competing for the Gβ13F/Gγ1 subunits of the heterotrimeric Gs protein complex. Loss of Gβ13F, Gγ1, or Gαs, but not any other G protein subunit, results in prevention of post-eclosion cell death and failure of the wing expansion. However, cell death prevention alone is not sufficient to induce the expansion defect, suggesting that the failure of epithelial-mesenchymal transition is key to the folded wing phenotypes. Overactivation of Gαs with cholera toxin mimics expression of constitutively activated Gαs and promotes wing blistering due to precocious cell death. In contrast, co-overexpression of Gβ13F and Gγ1 does not produce wing blistering, revealing the passive role of the Gβγ in the Gαs-mediated activation of apoptosis, but hinting at the possible function of Gβγ in the epithelial-mesenchymal transition. Our results provide a comprehensive functional analysis of the heterotrimeric G protein proteome in the late stages of Drosophila wing development.
Highlights
G protein-coupled receptors (GPCRs) represent the most populous receptor family in metazoans
380 non-olfactory GPCRs are encoded by the human genome [1], corroborated by ca. 250 GPCRs in insect genomes [2,3], making 1–1.5% of the total gene number dedicated to this receptor superfamily in invertebrates and mammals
GPCRs transmit their signals by activating heterotrimeric G protein complexes inside the cell
Summary
G protein-coupled receptors (GPCRs) represent the most populous receptor family in metazoans. 380 non-olfactory GPCRs are encoded by the human genome [1], corroborated by ca. 250 GPCRs in insect genomes [2,3], making 1–1.5% of the total gene number dedicated to this receptor superfamily in invertebrates and mammals. GPCRs transmit their signals by activating heterotrimeric G protein complexes inside the cell. A heterotrimeric G protein consists of a GDP-bound a-subunit and a bc-heterodimer. Ligandstimulated GPCR serves as a guanine nucleotide-exchange factor, activating the GDP-to-GTP exchange on the Ga-subunit. This leads to dissociation of the heterotrimeric complex into Ga-GTP and bc, which transmit the signal further inside the cell [4]
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