Novel isoforms of MeI1c melatonin receptors modulating intracellular cyclic guanosine 3',5'-monophosphate levels

R Jockers, L Petit, I Lacroix, P deCoppet, Perry Barrett, Peter John Morgan, B Guardiola, P Delagrange, S Marullo, A D Strosberg

Research output: Contribution to journalArticle

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Abstract

Two cDNAs encoding novel isoforms of Xenopus laevis melatonin receptors were cloned using PCR primers specific for the X. laevis-melanophore Mel(1c) melatonin receptor described in a recent publication. The novel isoforms were highly homologous to the described frog Mel(1c) cDNA, although the C-terminal tail of both was shorter by 65 amino acid residues. Nucleotide sequences of these novel isoforms, called Mel(1)c(alpha)) and Mel(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(1c(alpha)) and Mel(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-[I-125]iodomelatonin binding sites. Agonist stimulation of Mel(1c(alpha)) receptor was associated with the inhibition of cAMP accumulation stimulated by forskolin (IC50 approximate to 10(-10) M) in HeLa, Ltk(-), and human embryonic kidney 293 (HEK 293) cells. Mel(1c(beta)) receptor modulated cAMP in HeLa and HEK 293 cells but not in Ltk(-) 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, IC50 values (approximate to 10(-10) M for Mel(1c(beta)) and 10(-9) to 10(-7) M for Mel(1c(alpha)) and maximal inhibition levels showed that Mel(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(1c(alpha)) and Mel(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(1c) melatonin receptors display identical ligand-binding characteristics, but different potencies in modulating cAMP and cGMP levels through G(i)/G(o)-dependent pathways. Furthermore, to our knowledge, this study provides the first data on the modulation of intracellular cGMP levels by cloned melatonin receptors.

Original languageEnglish
Pages (from-to)1070-1081
Number of pages12
JournalMolecular Endocrinology
Volume11
Issue number8
DOIs
Publication statusPublished - Jul 1997

Keywords

  • G-protein
  • nitric-oxide
  • signal-transduction
  • guanylyl cyclase
  • 5-HT1A receptor
  • messenger-RNA
  • binding
  • expression
  • inhibition
  • brain

Cite this

Novel isoforms of MeI1c melatonin receptors modulating intracellular cyclic guanosine 3',5'-monophosphate levels. / Jockers, R ; Petit, L ; Lacroix, I ; deCoppet, P ; Barrett, Perry; Morgan, Peter John; Guardiola, B ; Delagrange, P ; Marullo, S ; Strosberg, A D .

In: Molecular Endocrinology, Vol. 11, No. 8, 07.1997, p. 1070-1081.

Research output: Contribution to journalArticle

Jockers, R, Petit, L, Lacroix, I, deCoppet, P, Barrett, P, Morgan, PJ, Guardiola, B, Delagrange, P, Marullo, S & Strosberg, AD 1997, 'Novel isoforms of MeI1c melatonin receptors modulating intracellular cyclic guanosine 3',5'-monophosphate levels', Molecular Endocrinology, vol. 11, no. 8, pp. 1070-1081. https://doi.org/10.1210/me.11.8.1070
Jockers, R ; Petit, L ; Lacroix, I ; deCoppet, P ; Barrett, Perry ; Morgan, Peter John ; Guardiola, B ; Delagrange, P ; Marullo, S ; Strosberg, A D . / Novel isoforms of MeI1c melatonin receptors modulating intracellular cyclic guanosine 3',5'-monophosphate levels. In: Molecular Endocrinology. 1997 ; Vol. 11, No. 8. pp. 1070-1081.
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abstract = "Two cDNAs encoding novel isoforms of Xenopus laevis melatonin receptors were cloned using PCR primers specific for the X. laevis-melanophore Mel(1c) melatonin receptor described in a recent publication. The novel isoforms were highly homologous to the described frog Mel(1c) cDNA, although the C-terminal tail of both was shorter by 65 amino acid residues. Nucleotide sequences of these novel isoforms, called Mel(1)c(alpha)) and Mel(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(1c(alpha)) and Mel(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-[I-125]iodomelatonin binding sites. Agonist stimulation of Mel(1c(alpha)) receptor was associated with the inhibition of cAMP accumulation stimulated by forskolin (IC50 approximate to 10(-10) M) in HeLa, Ltk(-), and human embryonic kidney 293 (HEK 293) cells. Mel(1c(beta)) receptor modulated cAMP in HeLa and HEK 293 cells but not in Ltk(-) 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, IC50 values (approximate to 10(-10) M for Mel(1c(beta)) and 10(-9) to 10(-7) M for Mel(1c(alpha)) and maximal inhibition levels showed that Mel(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(1c(alpha)) and Mel(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(1c) melatonin receptors display identical ligand-binding characteristics, but different potencies in modulating cAMP and cGMP levels through G(i)/G(o)-dependent pathways. Furthermore, to our knowledge, this study provides the first data on the modulation of intracellular cGMP levels by cloned melatonin receptors.",
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AU - Jockers, R

AU - Petit, L

AU - Lacroix, I

AU - deCoppet, P

AU - Barrett, Perry

AU - Morgan, Peter John

AU - Guardiola, B

AU - Delagrange, P

AU - Marullo, S

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N2 - Two cDNAs encoding novel isoforms of Xenopus laevis melatonin receptors were cloned using PCR primers specific for the X. laevis-melanophore Mel(1c) melatonin receptor described in a recent publication. The novel isoforms were highly homologous to the described frog Mel(1c) cDNA, although the C-terminal tail of both was shorter by 65 amino acid residues. Nucleotide sequences of these novel isoforms, called Mel(1)c(alpha)) and Mel(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(1c(alpha)) and Mel(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-[I-125]iodomelatonin binding sites. Agonist stimulation of Mel(1c(alpha)) receptor was associated with the inhibition of cAMP accumulation stimulated by forskolin (IC50 approximate to 10(-10) M) in HeLa, Ltk(-), and human embryonic kidney 293 (HEK 293) cells. Mel(1c(beta)) receptor modulated cAMP in HeLa and HEK 293 cells but not in Ltk(-) 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, IC50 values (approximate to 10(-10) M for Mel(1c(beta)) and 10(-9) to 10(-7) M for Mel(1c(alpha)) and maximal inhibition levels showed that Mel(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(1c(alpha)) and Mel(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(1c) melatonin receptors display identical ligand-binding characteristics, but different potencies in modulating cAMP and cGMP levels through G(i)/G(o)-dependent pathways. Furthermore, to our knowledge, this study provides the first data on the modulation of intracellular cGMP levels by cloned melatonin receptors.

AB - Two cDNAs encoding novel isoforms of Xenopus laevis melatonin receptors were cloned using PCR primers specific for the X. laevis-melanophore Mel(1c) melatonin receptor described in a recent publication. The novel isoforms were highly homologous to the described frog Mel(1c) cDNA, although the C-terminal tail of both was shorter by 65 amino acid residues. Nucleotide sequences of these novel isoforms, called Mel(1)c(alpha)) and Mel(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(1c(alpha)) and Mel(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-[I-125]iodomelatonin binding sites. Agonist stimulation of Mel(1c(alpha)) receptor was associated with the inhibition of cAMP accumulation stimulated by forskolin (IC50 approximate to 10(-10) M) in HeLa, Ltk(-), and human embryonic kidney 293 (HEK 293) cells. Mel(1c(beta)) receptor modulated cAMP in HeLa and HEK 293 cells but not in Ltk(-) 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, IC50 values (approximate to 10(-10) M for Mel(1c(beta)) and 10(-9) to 10(-7) M for Mel(1c(alpha)) and maximal inhibition levels showed that Mel(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(1c(alpha)) and Mel(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(1c) melatonin receptors display identical ligand-binding characteristics, but different potencies in modulating cAMP and cGMP levels through G(i)/G(o)-dependent pathways. Furthermore, to our knowledge, this study provides the first data on the modulation of intracellular cGMP levels by cloned melatonin receptors.

KW - G-protein

KW - nitric-oxide

KW - signal-transduction

KW - guanylyl cyclase

KW - 5-HT1A receptor

KW - messenger-RNA

KW - binding

KW - expression

KW - inhibition

KW - brain

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JO - Molecular Endocrinology

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SN - 0888-8809

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