Novel isoforms of Mel sub(1C) melatonin receptors modulating intracellular cyclic guanosine 3',5'-monophosphate levels

• Published in: Molecular endocrinology (Baltimore, Md.) Md.), 1997-07, Vol.11 (8), p.1070-1081
• Main Authors: Jockers, R, Petit, L, Lacroix, I, de Coppet, P, Barrett, P, Morgan, P J, Guardiola, B, Delagrange, P, Marullo, S, Strosberg, AD
• Format: Article
• Language: English
• ISSN: 0888-8809

Two cDNAs encoding novel isoforms of Xenopus laevis melatonin receptors were cloned using PCR primers specific for the X. laevis-melanophore Mel sub(1C) melatonin receptor described in a recent publication. The novel isoforms were highly homologous to the described frog Mel sub(1C) cDNA, although the C-terminal tail of both was shorter by 65 amino acid residues. Nucleotide sequences of these novel isoforms, called Mel sub(1C( alpha )) and Mel sub(1C( beta )), differed from each other by only 35 nucleotides and six amino acid residues. Studies on several animals of various Xenopus species indicate that Mel sub(1C( alpha )) and Mel sub(1C( beta )) receptors may correspond to allelic variants of the same locus. Studies on cells transfected with both receptor cDNAs showed the expression of high-affinity 2-[ super(125)I]iodomelatonin binding sites. Agonist stimulation of Mel sub(1C( alpha )) receptor was associated with the inhibition of cAMP accumulation stimulated by forskolin (IC sub(50) approximately 10 super(-10) M) in HeLa, Ltk super(-), and human embryonic kidney 293 (HEK 293) cells. Mel sub(1C( beta )) receptor modulated cAMP in HeLa and HEK 293 cells but not in Ltk super(-) cells. Both receptors inhibited, in a dose-dependent manner, cGMP accumulation in all three cell lines incubated with a phosphodiesterase inhibitor. This effect was localized upstream of soluble guanylyl cyclase and was blocked by pertussis toxin treatment. However, IC sub(50) values ( approximately 10 super(-10) M for Mel sub(1C( beta )) and 10 super(-9) to 10 super(-7) M for Mel sub(1C( alpha ))) and maximal inhibition levels showed that Mel sub(1C( alpha )) receptors are much less efficiently coupled to the cGMP pathway. Coupling differences may be explained by the fact that five of the six amino acid substitutions between Mel sub(1C( alpha )) and Mel sub(1C( beta )) receptors are located within cytoplasmic regions potentially involved in signal transduction. The existence of coupling differences is in agreement with the observation that expression of both receptors is evolutionally conserved in native tissue. In conclusion, two novel, potentially allelic, isoforms of Xenopus Mel sub(1C) melatonin receptors display identical ligand-binding characteristics, but different potencies in modulating cAMP and cGMP levels through G sub(i)/G sub(o)-dependent pathways. Furthermore, to our knowledge, this study provides the first data on the modulation of intracellular cGMP levels by cloned