The interaction of MC3R and MC4R with MRAP2a in rainbow trout (Oncorhynchus mykiss)
Melanocortin 3 and 4 receptors are two important neural G protein-coupled receptors that regulate energy homeostasis in vertebrates. Melanocortin receptor accessory protein 2 (MRAP2) is also involved in the regulation of food intake and body weight as a variable regulator of melanocortin receptors....
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Veröffentlicht in: | Fish physiology and biochemistry 2023-02, Vol.49 (1), p.61-74 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Melanocortin 3 and 4 receptors are two important neural G protein-coupled receptors that regulate energy homeostasis in vertebrates. Melanocortin receptor accessory protein 2 (MRAP2) is also involved in the regulation of food intake and body weight as a variable regulator of melanocortin receptors. Rainbow trout (
Oncorhynchus mykiss
) is a valuable cold-water fish cultured worldwide. In the rainbow trout model, we cloned and identified
mrap2a
, a paralog of
mrap2
. Rainbow trout
mrap2a
consisted of a 690 bp ORF and was expected to encode a putative protein of 229 amino acids. The qPCR results showed that rainbow trout
mrap2a
was expressed at high levels in brain tissue similar to
mc3r
and
mc4r
. In addition, co-immunoprecipitation verified that MRAP2a interacts with MC3R and MC4R in vitro and that MRAP2a is involved in and regulates the constitutive activity and signaling of MC3R and MC4R. MRAP2a reduced constitutive and agonist-stimulated cAMP levels of MC3R; furthermore, MRAP2a increased constitutive ERK1/2 activation but reduced ligand-induced stimulation at high levels of expression. For MC4R, MRAP2a showed decreased cAMP basal activity but increased agonist-stimulated cAMP signaling and increased ACTH ligand sensitivity. However, MRAP2a failed to affect MC4R constitutive activity and agonist-induced ERK1/2 signaling. Undoubtedly, our study will have great significance for revealing the conserved role of MC4R and MC3R signaling in teleost fish, especially in cold-water fish growth and energy homeostasis. |
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ISSN: | 0920-1742 1573-5168 |
DOI: | 10.1007/s10695-022-01159-0 |