Signal pathway analysis of selected obesity-associated melanocortin-4 receptor class V mutants.

Sunita Sharma, Stephanie Thibodeau, Jonathan Lytton

Biochimica et biophysica acta. Molecular basis of disease 2020 Aug 01

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Mutations in the melanocortin-4 receptor (MC4R) in humans are the single most common cause of rare monogenic 1severe obesity, and polymorphisms in this gene are also associated with obesity in the general population. The MC4R is a G-protein coupled receptor, and in vitro analysis suggests that MC4R can signal through several different G-protein subtypes. In vivo studies show complex outcomes, with different G-proteins in different cells responsible for different physiological responses linked to obesity. There is an emerging consensus that Gαq-linked signals in the paraventricular nucleus of the hypothalamus are essential for normal satiety and the control of feeding behavior. Many MC4R mutations have been analyzed for the molecular defect underlying their association with obesity, which has revealed a group - referred to as class V mutants - with no measurable change in receptor function. However, Gαq-linked signaling leading to Ca2+ release has only been examined for a few MC4R mutations. In this study, we have examined seven MC4R class V mutants, as well as two other well-characterized signal-defective mutants as controls, with respect to G-protein signaling coupled to cAMP production, mitogen-activated protein kinase (MAPK) activation, and Ca2+ release. These data confirm, with one exception (E308K), the expected pattern of cAMP and MAPK signaling for wild type and mutant MC4R. Our results also demonstrate normal MSH-induced Ca2+ signals for wild type as well as all the class V mutants, but not the signal-defective controls. Thus, the means by which class V MC4R mutations lead to obesity remains an open question. Copyright © 2020 Elsevier B.V. All rights reserved.

Citation

Sunita Sharma, Stephanie Thibodeau, Jonathan Lytton. Signal pathway analysis of selected obesity-associated melanocortin-4 receptor class V mutants. Biochimica et biophysica acta. Molecular basis of disease. 2020 Aug 01;1866(8):165835