| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2572458 | Trends in Pharmacological Sciences | 2016 | 11 Pages |
The G protein-coupled receptor (GPCR) Smoothened (Smo) is the signal transducer of the developmentally and therapeutically relevant Hedgehog (Hh) pathway. Although recent structural analyses have advanced our understanding of Smo biology, several questions remain. Chief among them are the identity of its natural ligand, the regulatory processes controlling its activation, and the mechanisms by which it signals to downstream effectors. In this review, we discuss recent discoveries from multiple model systems that have set the stage for solving these mysteries. We focus on the roles of distinct Smo functional domains, post-translational modifications, and trafficking, and conclude by discussing their contributions to signal output.
TrendsRecent structural information reveals how ligands bind and regulate Smoothened.Smoothened signaling is regulated by its trafficking within the primary cilium.Smoothened can signal through G protein-dependent and -independent mechanisms.
