# Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balance

## TL;DR

This study shows that the melanocortin 3 receptor (MC3R) is more involved in controlling puberty than obesity across humans, dogs, and mice.

## Contribution

The study provides cross-species evidence that MC3R deficiency affects pubertal timing but not obesity in mammals.

## Key findings

- Complete loss of MC3R function does not result in obesity in humans.
- Dogs with a common MC3R mutation are lighter and have delayed puberty.
- MC3R influences pubertal timing in humans, mice, and dogs.

## Abstract

Hypothalamic neurons expressing either POMC or AGRP sense nutritional state directly and indirectly and transmit these neuropeptide signals to other brain centres through the melanocortin 3 and 4 receptors. MC4R is primarily concerned with the control of appetite and energy expenditure while MC3R is more closely related to the control of linear growth and the timing of puberty. The role of MC3R in the long-term control of energy balance and body composition is less clear, particularly in humans. We have undertaken studies in humans, domestic dogs and mice with the goal of clarifying the relative impact of MC3R deficiency on energy balance, growth and sexual development. By studying three large consanguineously enriched cohorts, totalling approximately 300K people, we identified nine individuals who are homozygous for functionally null MC3R variants. The body mass index (BMI) of the homozygous MC3R variant carriers was not significantly different from that of age, sex and demographically matched controls, with six of the nine homozygotes having a BMI <30 kg/m2.

We detected a canine MC3R missense variant (p.M320I) which is common in labrador retrievers and showed that this significantly impairs receptor signalling. Dogs homozygous for p.M320I were lighter and showed delayed pubertal development but were not significantly more obese than wild-type or heterozygous dogs. We also established that the lack of Mc3r delayed pubertal development in both male and female mice.

Finally, we studied growth and pubertal trajectories of individuals carrying rare loss-of-function MC3R variants and found that male carriers had delayed peak weight velocity and genital development but had no evidence for excess body fat compared to non-carriers.

Our results support MC3R having a conserved role across mammals in controlling growth and pubertal timing. While MC3R deficiency may influence linear growth and body composition, complete loss of MC3R does not result in a penetrant human obesity syndrome.

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•Complete loss of MC3R function does not result in obesity in humans.•Dogs with a common MC3R mutation are lighter and have delayed puberty.•MC3R influences pubertal timing in humans, mice and dogs.

Complete loss of MC3R function does not result in obesity in humans.

Dogs with a common MC3R mutation are lighter and have delayed puberty.

MC3R influences pubertal timing in humans, mice and dogs.