Genetic determinants of hair and eye colours in the Scottish and Danish populations

BackgroundEye and hair colour is highly variable in the European population, and is largely genetically determined. Both linkage and association studies have previously been used to identify candidate genes underlying this variation. Many of the genes found were previously known as underlying mutant mouse phenotypes or human genetic disease, but others, previously unsuspected as pigmentation genes, have also been discovered.ResultsWe assayed the hair of a population of individuals of Scottish origin using tristimulus colorimetry, in order to produce a quantitative measure of hair colour. Cluster analysis of this data defined two groups, with overlapping borders, which corresponded to visually assessed dark versus red/light hair colour. The Danish population was assigned into categorical hair colour groups. Both cohorts were also assessed for eye colour. DNA from the Scottish group was genotyped at SNPs in 33 candidate genes, using 384 SNPs identified by HapMap as representatives of each gene. Associations found between SNPs and colorimetric hair data and eye colour categories were replicated in a cohort of the Danish population. The Danish population was also genotyped with SNPs in 4 previously described pigmentation genes. We found replicable associations of hair colour with the KITLG and OCA2 genes. MC1R variation correlated, as expected, with the red dimension of colorimetric hair colour in Scots. The Danish analysis excluded those with red hair, and no associations were found with MC1R in this group, emphasising that MC1R regulates the colour rather than the intensity of pigmentation. A previously unreported association with the HPS3 gene was seen in the Scottish population. However, although this replicated in the smaller cohort of the Danish population, no association was seen when the whole study population was analysed.ConclusionsWe have found novel associations with SNPs in known pigmentation genes and colorimetrically assessed hair colour in a Scottish and a Danish population.

[1]  R. Swank,et al.  Cocoa: a new mouse model for platelet storage pool deficiency , 1988, British journal of haematology.

[2]  Snæbjörn Pálsson,et al.  Two newly identified genetic determinants of pigmentation in Europeans , 2008, Nature Genetics.

[3]  H. Eiberg,et al.  Assignment of Genes Coding for Brown Eye Colour (BEY2) and Brown Hair Colour (HCL3) on Chromosome 15q , 1996, European journal of human genetics : EJHG.

[4]  S. Baindur-Hudson,et al.  Hair color measurement and variation. , 2008, American journal of physical anthropology.

[5]  R. Swank,et al.  Murine Hermansky–Pudlak syndrome genes: regulators of lysosome‐related organelles , 2004, BioEssays : news and reviews in molecular, cellular and developmental biology.

[6]  R. Sturm,et al.  Molecular genetics of human pigmentation diversity. , 2009, Human molecular genetics.

[7]  R. Spritz,et al.  Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity. , 1998, American journal of human genetics.

[8]  Mark Daly,et al.  Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..

[9]  Ian Jackson,et al.  Variants of the melanocyte–stimulating hormone receptor gene are associated with red hair and fair skin in humans , 1995, Nature Genetics.

[10]  K. Gunderson,et al.  Illumina, Inc. , 2005, Pharmacogenomics.

[11]  D. Duffy,et al.  Spectrophotometric Methods for Quantifying Pigmentation in Human Hair—Influence of MC1R Genotype and Environment , 2008, Photochemistry and photobiology.

[12]  Johan T den Dunnen,et al.  Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene. , 2008, American journal of human genetics.

[13]  I. Jackson,et al.  Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation. , 2000, Human molecular genetics.

[14]  Hans Eiberg,et al.  Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression , 2008, Human Genetics.

[15]  B. Roe,et al.  The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene. , 2001, Genomics.

[16]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[17]  D. Duffy,et al.  Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: the effect of OCA2 and HERC2. , 2008, The Journal of investigative dermatology.

[18]  Maria L. Wei Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function. , 2006, Pigment cell research.

[19]  G. Harrison,et al.  Differences in human pigmentation: measurement, geographic variation, and causes. , 1973, The Journal of investigative dermatology.

[20]  Richard Hodgson,et al.  Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation , 2005, Human mutation.

[21]  K. Steel,et al.  TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor. , 1992, Development.

[22]  Wei Chen,et al.  Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. , 2003, Human molecular genetics.

[23]  H. Eiberg,et al.  Determination of cis/trans phase of variations in the MC1R gene with allele‐specific PCR and single base extension , 2008, Electrophoresis.

[24]  Snæbjörn Pálsson,et al.  Genetic determinants of hair, eye and skin pigmentation in Europeans , 2007, Nature Genetics.

[25]  D Bentley,et al.  Highly parallel SNP genotyping. , 2003, Cold Spring Harbor symposia on quantitative biology.

[26]  J. Rees,et al.  The relation between melanocortin 1 receptor (MC1R) variation and the generation of phenotypic diversity in the cutaneous response to ultraviolet radiation , 2005, Peptides.

[27]  A. Urquhart,et al.  Sequence polymorphism in the human melanocortin 1 receptor gene as an indicator of the red hair phenotype. , 2001, Forensic science international.

[28]  R. Millikan,et al.  Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma. , 2006, Cancer research.

[29]  F. Hu,et al.  A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation , 2008, PLoS genetics.

[30]  Nicholas G Martin,et al.  A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color. , 2008, American journal of human genetics.