Cloning and functional pharmacology of two corticotropin-releasing factor receptors from a teleost fish

Although it is well established that fish possess corticotropin-releasing factor (CRF) and a CRF-like peptide, urotensin I, comparatively little is known about the pharmacology of their cognate receptors. Here we report the isolation and functional expression of two complementary DNAs (cDNAs), from the chum salmon Oncorhynchus keta, which encode orthologues of the mammalian and amphibian CRF type 1 (CRF) and type 2 (CRF2) receptors. Radioligand competition binding experiments have revealed that the salmon CRF1 and CRF2 receptors bind urotensin I with similar to 8-fold higher affinity than rat/human CRF. These two peptides. together with two related CRF-like peptides, namely, sauvagine and urocortin, were also tested in cAMP assays; for cells expressing the salmon CRF1 receptor, EC50 values for the stimulation of cAMP production were between 4.5 +/- 1.8 and 15.3 +/- 3.1 nM. For the salmon CRF2 receptor, the corresponding values were: rat/human CRF, 9.4 +/- 0.4 nM; urotensin I, 21.2 +/- 2.1 nM; sauvagine, 0.7 +/- 0.1 nM; and urocortin, 2.2 +/- 0.7 nM. We have also functionally coupled the O. keta CRF1 receptor, in Xenopus laevis oocytes, to the endogenous Ca2+-activated chloride conductance by co-expression with the G-protein alpha subunit, G(alpha 16). The EC50 value for channel activation by rat/human CRF (11.2 +/- 2.6 nM) agrees well with that obtained in cAMP assays (15.3 +/- 3.1 nM). We conclude that although sauvagine is 13- and 30-fold more potent than rat/human CRF and urotensin I, respectively, in activating the salmon CRF2 receptor, neither receptor appears able to discriminate between the native ligands. CRF and urotensin I. (C) 2001 Elsevier Science B.V. All rights reserved.