Feedback control of the Gpr161-GαS-PKA axis contributes to basal Hedgehog repression in zebrafish

Hedgehog (Hh) ligands act as morphogens to direct patterning and proliferation during embryonic development. Protein kinase A (PKA) is a central negative regulator of Hh signalling, and in the absence of Hh ligands, PKA activity prevents inappropriate expression of Hh target genes. The orphan G-protein-coupled receptor Gpr161 contributes to the basal Hh repression machinery by activating PKA. Gpr161 acts as an A-kinase-anchoring protein, and is itself phosphorylated by PKA, but the functional significance of PKA phosphorylation of Gpr161 in the context of Hh signalling remains unknown. Here, we show that loss of Gpr161 in zebrafish leads to constitutive activation of medium and low, but not maximal, levels of Hh target gene expression. Furthermore, we find that PKA phosphorylation-deficient forms of Gpr161, which we show directly couple to Gas, display an increased sensitivity to Shh, resulting in excess high-level Hh signalling. Our results suggest that PKA feedback-mediated phosphorylation of Gpr161 may provide a mechanism for fine-tuning Gpr161 ciliary localisation and PKA activity.

Automated summary

In this study, Gpr161 was found to play a crucial role in negatively regulating the Hh signaling pathway by activating PKA to inhibit the expression of Hh target genes. Additionally, PKA phosphorylation-deficient forms of Gpr161 were shown to increase sensitivity to Shh, resulting in excessive high-level Hh signaling. These findings suggest that PKA-mediated phosphorylation of Gpr161 may provide a mechanism for fine-tuning Gpr161 ciliary localization and PKA activity.