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Resources » Paper

Lockyer JL et al. (2024) Proc Natl Acad Sci U S A "Selective optogenetic inhibition of Gαq or Gαi signaling by minimal RGS domains disrupts circuit functionality and circuit formation."

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  • Comments on Lockyer JL et al. (2024) Proc Natl Acad Sci U S A "Selective optogenetic inhibition of Gαq or Gαi signaling by minimal RGS domains disrupts circuit functionality and circuit formation." (0)

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    PMID:
    Status:
    Publication type:
    Journal_article
    WormBase ID:
    WBPaper00067190

    Lockyer JL, Reading A, Vicenzi S, Zbela A, Viswanathan S, Delandre C, Newland JW, McMullen JPD, Marshall OJ, Gasperini R, Foa L, & Lin JY (2024). Selective optogenetic inhibition of Gαq or Gαi signaling by minimal RGS domains disrupts circuit functionality and circuit formation. Proc Natl Acad Sci U S A, 121, e2411846121. doi:10.1073/pnas.2411846121

    Optogenetic techniques provide genetically targeted, spatially and temporally precise approaches to correlate cellular activities and physiological outcomes. In the nervous system, G protein-coupled receptors (GPCRs) have essential neuromodulatory functions through binding extracellular ligands to induce intracellular signaling cascades. In this work, we develop and validate an optogenetic tool that disrupts G&#x3b1;<sub>q</sub> signaling through membrane recruitment of a minimal regulator of G protein signaling (RGS) domain. This approach, Photo-induced G&#x3b1; Modulator-Inhibition of G&#x3b1;<sub>q</sub> (PiGM-Iq), exhibited potent and selective inhibition of G&#x3b1;<sub>q</sub> signaling. Using PiGM-Iq we alter the behavior of <i>Caenorhabditis elegans</i> and <i>Drosophila</i> with outcomes consistent with GPCR-G&#x3b1;<sub>q</sub> disruption. PiGM-Iq changes axon guidance in cultured dorsal root ganglia neurons in response to serotonin. PiGM-Iq activation leads to developmental deficits in zebrafish embryos and larvae resulting in altered neuronal wiring and behavior. Furthermore, by altering the minimal RGS domain, we show that this approach is amenable to G&#x3b1;<sub>i</sub> signaling. Our unique and robust optogenetic G&#x3b1; inhibiting approaches complement existing neurobiological tools and can be used to investigate the functional effects neuromodulators that signal through GPCR and trimeric G proteins.

    Authors: Lockyer JL, Reading A, Vicenzi S, Zbela A, Viswanathan S, Delandre C, Newland JW, McMullen JPD, Marshall OJ, Gasperini R, Foa L, Lin JY


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