Abstract
G-protein β subunits perform essential neuronal functions as part of G-protein βγ and Gβ5-regulators of G-protein signaling (RGS) complexes. Both Gβγ and Gβ5-RGS are obligate dimers that are thought to require the assistance of the cytosolic chaperonin CCT and a cochaperone, phosducin-like protein 1 (PhLP1) for dimer formation. To test this hypothesis in vivo, we deleted the Phlp1 gene in mouse (Mus musculus) retinal rod photoreceptor cells and measured the effects on G-protein biogenesis and visual signal transduction. In the PhLP1-depleted rods, Gβγ dimer formation was decreased 50-fold, resulting in a >10-fold decrease in light sensitivity. Moreover, a 20-fold reduction in Gβ5 and RGS9-1 expression was also observed, causing a 15-fold delay in the shutoff of light responses. These findings conclusively demonstrate in vivo that PhLP1 is required for the folding and assembly of both Gβγ and Gβ5-RGS9. © 2013 the authors.
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CITATION STYLE
Lai, C. W. J., Kolesnikov, A. V., Frederick, J. M., Blake, D. R., Jiang, L., Stewart, J. S., … Willardson, B. M. (2013). Phosducin-like protein 1 is essential for G-protein assembly and signaling in retinal rod photoreceptors. Journal of Neuroscience, 33(18), 7941–7951. https://doi.org/10.1523/JNEUROSCI.5001-12.2013
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