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Genetic studies of the human melanocortin-1 receptor

Lookup NU author(s): Professor Jonathan Rees, Professor Mark Birch-Machin, Dr Niamh Flanagan, Dr Eugene Healy

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Abstract

Genetic approaches have suggested a critical role for the melanocortin-1 receptor in the control of pigmentation. We showed that this gene is unusually polymorphic in European populations and that, of the many variants, three in particular appear to be associated with red hair or fair skin. Family studies suggest these are inherited as an autosomal recessive trait (or at least approximate to this in many families). To date all individuals with two of these three changes (homozygote or compound heterozygote) have red hair. Early functional studies are in keeping with defective signalling through MC1R. An interested and perhaps unexpected question relates to the evolutionary factors that have given rise to such variants. Two models can be proposed, that are based on multiple alleles with minor changes in function or genetic hitch-hicking.


Publication metadata

Author(s): Rees JL, Birch-Machin M, Flanagan N, Healy E, Phillips S, Todd C

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Cutaneous Neuroimmunomodulation: The Proopiomelanocortin System

Year of Conference: 1999

Pages: 134-142

ISSN: 0077-8923

Publisher: Wiley-Blackwell Publishing, Inc.

URL: http://dx.doi.org/10.1111/j.1749-6632.1999.tb08670.x

DOI: 10.1111/j.1749-6632.1999.tb08670.x

PubMed id: 10816646

Series Title: Annals of the New York Academy of Sciences


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