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Interaction of retinal guanylate cyclase with the alpha subunit of transducin: potential role in transducin localization
Journal article   Open access   Peer reviewed

Interaction of retinal guanylate cyclase with the alpha subunit of transducin: potential role in transducin localization

Derek H Rosenzweig, K Saidas Nair, Konstantin Levay, Igor V Peshenko, John W Crabb, Alexander M Dizhoor and Vladlen Z Slepak
Biochemical journal, v 417(3), pp 803-812
01 Feb 2009
PMID: 18840097
url
https://europepmc.org/articles/pmc3312023View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

Animals Cattle Cells, Cultured Cercopithecus aethiops COS Cells Guanylate Cyclase - genetics Guanylate Cyclase - metabolism Humans Immunoprecipitation Mice Mice, Knockout Protein Subunits - analysis Protein Subunits - metabolism Retina - enzymology Retina - metabolism Transducin - analysis Transducin - metabolism Transfection
Vertebrate phototransduction is mediated by cGMP, which is generated by retGC (retinal guanylate cyclase) and degraded by cGMP phosphodiesterase. Light stimulates cGMP hydrolysis via the G-protein transducin, which directly binds to and activates phosphodiesterase. Bright light also causes relocalization of transducin from the OS (outer segments) of the rod cells to the inner compartments. In the present study, we show experimental evidence for a previously unknown interaction between G(alphat) (the transducin alpha subunit) and retGC. G(alphat) co-immunoprecipitates with retGC from the retina or from co-transfected COS-7 cells. The retGC-G(alphat) complex is also present in cones. The interaction also occurs in mice lacking RGS9 (regulator of G-protein signalling 9), a protein previously shown to associate with both G(alphat) and retGC. The G(alphat)-retGC interaction is mediated primarily by the kinase homology domain of retGC, which binds GDP-bound G(alphat) stronger than the GTP[S] (GTPgammaS; guanosine 5'-[gamma-thio]triphosphate) form. Neither G(alphat) nor G(betagamma) affect retGC-mediated cGMP synthesis, regardless of the presence of GCAP (guanylate cyclase activating protein) and Ca2+. The rate of light-dependent transducin redistribution from the OS to the inner segments is markedly accelerated in the retGC-1-knockout mice, while the migration of transducin to the OS after the onset of darkness is delayed. Supplementation of permeabilized photoreceptors with cGMP does not affect transducin translocation. Taken together, these results suggest that the protein-protein interaction between G(alphat) and retGC represents a novel mechanism regulating light-dependent translocation of transducin in rod photoreceptors.

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Collaboration types
Domestic collaboration
Web of Science research areas
Biochemistry & Molecular Biology
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