RT Journal Article SR Electronic T1 Smoothened Is a Fully Competent Activator of the Heterotrimeric G Protein Gi JF Molecular Pharmacology JO Mol Pharmacol FD American Society for Pharmacology and Experimental Therapeutics SP 691 OP 697 DO 10.1124/mol.112.082511 VO 83 IS 3 A1 Feng Shen A1 Lan Cheng A1 Andrew E. Douglas A1 Natalia A. Riobo A1 David R. Manning YR 2013 UL http://molpharm.aspetjournals.org/content/83/3/691.abstract AB Smoothened (Smo) is a 7-transmembrane protein essential to the activation of Gli transcription factors (Gli) by hedgehog morphogens. The structure of Smo implies interactions with heterotrimeric G proteins, but the degree to which G proteins participate in the actions of hedgehogs remains controversial. We posit that the Gi family of G proteins provides to hedgehogs the ability to expand well beyond the bounds of Gli. In this regard, we evaluate here the efficacy of Smo as it relates to the activation of Gi, by comparing Smo with the 5-hydroxytryptamine1A (5-HT1A) receptor, a quintessential Gi-coupled receptor. We find that with use of [35S]guanosine 5′-(3-O-thio)triphosphate, first, with forms of Gi endogenous to human embryonic kidney (HEK)-293 cells made to express epitope-tagged receptors and, second, with individual forms of Gαi fused to the C terminus of each receptor, Smo is equivalent to the 5-HT1A receptor in the assay as it relates to capacity to activate Gi. This finding is true regardless of subtype of Gi (e.g., Gi2, Go, and Gz) tested. We also find that Smo endogenous to HEK-293 cells, ostensibly through inhibition of adenylyl cyclase, decreases intracellular levels of cAMP. The results indicate that Smo is a receptor that can engage not only Gli but also other more immediate effectors.