Nucleotide diversity and population differentiation of the melanocortin 1 receptor gene, MC1R

BMC Genet. 2008 Apr 10:9:31. doi: 10.1186/1471-2156-9-31.

Abstract

Background: The melanocortin 1 receptor gene (MC1R) is responsible for normal pigment variation in humans and is highly polymorphic with numerous population-specific alleles. Some MC1R variants have been associated with skin cancer risk.

Results: Allele frequency data were compiled on 55 single nucleotide polymorphisms from seven geographically distinct human populations (n = 2306 individuals). MC1R nucleotide diversity, pi, was much higher (10.1 x 10-4) than in other genes for all subjects. A large degree of population differentiation, determined by FST, was also present, particularly between Asia and all other populations, due to the p.R163Q (c.488 G>A) polymorphism. The least amount of differentiation was between the United States, Northern Europe, and Southern Europe. Tajima's D statistic suggested the presence of positive selection in individuals from Europe.

Conclusion: This study further quantifies the degree of population-specific genetic variation and suggests that positive selection may be present in European populations in MC1R.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Intramural

MeSH terms

  • Alleles
  • Base Sequence
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genetic Variation*
  • Humans
  • Melanoma / genetics
  • Polymorphism, Single Nucleotide
  • Receptor, Melanocortin, Type 1 / genetics*
  • Selection, Genetic
  • Skin Neoplasms / genetics
  • Skin Pigmentation / genetics*

Substances

  • Receptor, Melanocortin, Type 1