Gsα stimulation of mammalian adenylate cyclases regulated by their hexahelical membrane anchors

• Published in: Cellular signalling 2020-04, Vol.68, p.109538-109538, Article 109538
• Main Authors: Seth, Anubha, Finkbeiner, Manuel, Grischin, Julia, Schultz, Joachim E.
• Format: Article
• Language: English
• Subjects: Adenylate cyclases; Cyclic AMP; Membrane anchor; Quorum-sensor; Receptor
• ISSN: 0898-6568; 1873-3913
• DOI: 10.1016/j.cellsig.2020.109538

Mammalian adenylate cyclases (ACs) are pseudoheterodimers with dissimilar hexahelical membrane-anchors, isoform-specifically conserved for more than half a billion years. We exchanged both membrane anchors of the AC isoform 2 by the quorum-sensing receptor from Vibrio harveyi, CqsS, which has a ligand, Cholera-Autoinducer-1 (CAI-1). In the chimera, AC activity was stimulated by Gsα, CAI-1 had no effect. Surprisingly, CAI-1 inhibited Gsα stimulation. We report that Gsα stimulation of human AC isoforms 2, 3, 5, and 9 expressed in Sf9 cells is inhibited by serum as is AC activity in membranes isolated from rat brain cortex. AC2 activation by forskolin or forskolin/Gsα was similarly inhibited. Obviously, serum contains as yet unidentified factors affecting AC activity. The data establish a linkage in ACs, in which the membrane anchors, as receptors, transduce extracellular signals to the cytosolic catalytic dimer. A mechanistic three state model of AC regulation is presented compatible with all known regulatory inputs into mammalian ACs. The data allow designating the membrane anchors of mammalian ACs as orphan receptors, and establish a new level of AC regulation. •Quorum sensing receptor from Vibrio impairs Gsα response of adenylate cyclase isoform 2 in respective chimera.•Human serum impairs Gsα responses in human adenylate cyclases 2, 3, 5, and 9.•Forskolin activation of adenylate cyclase 2 impaired by human serum.•Three state model of adenylate cyclase regulation proposed.•Membrane anchors of adenylate cyclases are orphan receptors.