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Melanocortin MC₁ receptor in human genetics and model systems.

Authors
  • Ka, Beaumont
  • Ss, Wong
  • Sa, Ainger
  • Yy, Liu
  • Mp, Patel
  • Glenn Millhauser
  • Jj, Smith
  • Pf, Alewood
  • Jh, Leonard
  • Ra, Sturm
Type
Published Article
Journal
European Journal of Pharmacology
Publisher
Elsevier
Publication Date
Jun 25, 2011
Volume
660
Issue
1
Pages
103–110
Identifiers
DOI: 10.1016/j.ejphar.2010.11.040
PMID: 21199646
PMCID: PMC3095693
Source
UCSC Neuro biomedical-ucsc
License
Green

Abstract

The melanocortin MC(1) receptor is a G-protein coupled receptor expressed in the melanocytes of the skin and hair and is known for its key role in the regulation of human pigmentation. Melanocortin MC(1) receptor activation after ultraviolet radiation exposure results in a switch from the red/yellow pheomelanin to the brown/black eumelanin pigment synthesis within cutaneous melanocytes; this pigment is then transferred to the surrounding keratinocytes of the skin. The increase in melanin maturation and uptake results in tanning of the skin, providing a physical protection of skin cells from ultraviolet radiation induced DNA damage. Melanocortin MC(1) receptor polymorphism is widespread within the Caucasian population and some variant alleles are associated with red hair colour, fair skin, poor tanning and increased risk of skin cancer. Here we will discuss the use of mouse coat colour models, human genetic association studies, and in vitro cell culture studies to determine the complex functions of the melanocortin MC(1) receptor and the molecular mechanisms underlying the association between melanocortin MC(1) receptor variant alleles and the red hair colour phenotype. Recent research indicates that melanocortin MC(1) receptor has many non-pigmentary functions, and that the increased risk of skin cancer conferred by melanocortin MC(1) receptor variant alleles is to some extent independent of pigmentation phenotypes. The use of new transgenic mouse models, the study of novel melanocortin MC(1) receptor response genes and the use of more advanced human skin models such as 3D skin reconstruction may provide key elements in understanding the pharmacogenetics of human melanocortin MC(1) receptor polymorphism.

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