Characterization of the Mel1c melatoninergic receptor in platypus (Ornithorhynchus anatinus)
Author(s) -
Célia Gautier,
SophiePénélope Guenin,
Isabelle RiestFery,
Tahlia Perry,
Céline Legros,
Olivier Nosjean,
V. Simonneaux,
Frank Grützner,
Jean A. Boutin
Publication year - 2018
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0191904
Subject(s) - platypus , melatonin , monotreme , melatonin receptor , biology , receptor , functional divergence , vertebrate , lineage (genetic) , mammal , zoology , evolutionary biology , genetics , endocrinology , gene , gene expression , taxonomy (biology) , gene family , systematics
Melatonin is a neurohormone produced in both animals and plants. It binds at least three G-protein-coupled receptors: MT 1 and MT 2 , and Mel1cGPR. Mammalian GPR50 evolved from the reptilian/avian Mel1c and lost its capacity to bind melatonin in all the therian mammal species that have been tested. In order to determine if binding is lost in the oldest surviving mammalian lineage of monotremes we investigated whether the melatonin receptor has the ability to bind melatonin in the platypus ( Ornithorhynchus anatinus ), and evaluated its pharmacological profile. Sequence and phylogenetic analysis showed that platypus has in fact retained the ancestral Mel1c and has the capacity to bind melatonin similar to other mammalian melatonin receptors (MT 1 and MT 2 ), with an affinity in the 1 nM range. We also investigated the binding of a set of melatoninergic ligands used previously to characterize the molecular pharmacology of the melatonin receptors from sheep, rats, mice, and humans and found that the general profiles of these compounds make Mel1c resemble human MT 1 more than MT 2 . This work shows that the loss of GPR50 binding evolved after the divergence of monotremes less than 190MYA in therian mammals.
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