Abstract

The genotype of a single SNP, rs12913832, is the primary predictor of blue and brown eye colours. The genotypes rs12913832:AA and rs12913832:GA are most often observed in individuals with brown eye colours, whereas rs12913832:GG is most often observed in individuals with blue eye colours. However, approximately 3% of Europeans with the rs12913832:GG genotype have brown eye colours. The purpose of the study presented here was to identify variants that explain brown eye colour formation in individuals with the rs12913832:GG genotype. Genes and regulatory regions surrounding SLC24A4, TYRP1, SLC24A5, IRF4, TYR, and SLC45A2, as well as the upstream region of OCA2 within the HERC2 gene were sequenced in a study comprising 40 individuals with the rs12913832:GG genotype. Of these, 24 individuals were considered to have blue eye colours and 16 individuals were considered to have brown eye colours. We identified 211 variants within the SLC24A4, TYRP1, IRF4, and TYR target regions associated with eye colour. Based on in silico analyses of predicted variant effects we recognized four variants, TYRP1 rs35866166:C, TYRP1 rs62538956:C, SLC24A4 rs1289469:C, and TYR rs1126809:G, to be the most promising candidates for explanation of brown eye colour in individuals with the rs12913832:GG genotype. Of the 16 individuals with brown eye colours, 14 individuals had four alleles, whereas the alleles were rare in the blue eyed individuals. rs35866166, rs62538956, and rs1289469 were for the first time found to be associated with pigmentary traits, whilst rs1126809 was previously found to be associated with pigmentary variation. To improve prediction of eye colours we suggest that future eye colour prediction models should include rs35866166, rs62538956, rs1289469, and rs1126809.

Highlights

  • The genetics behind human eye colour has been extensively studied

  • Genes and regulatory regions surrounding the pigmentary genes SLC24A4, TYRP1, SLC24A5, IRF4, TYR, and SLC45A2, as well as the upstream region of OCA2 within HERC2 were investigated with massively parallel sequencing (MPS) in 40 rs12913832:GG individuals with different eye colours that were determined by quantitative eye colour measurements

  • SNPs associated with brown eye colour in individuals with the rs12913832:GG genotype located in regulatory regions were analysed with PROMO version 3.0.2 [23, 24] using default search settings

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Summary

Introduction

The genetics behind human eye colour has been extensively studied. The SNP rs12913832 is strongly associated with eye colour and a good predictor of blue and brown eye colours [1, 2]. rs12913832 is located in the promoter region of OCA2 and influences the transcription of OCA2 [3]. The rs12913832:G allele has a negative effect on OCA2 expression and the production of eumelanin [3] For this reason, individuals with the genotype rs12913832:GG are expected to have blue eyes, while individuals with the genotypes rs12913832:AA or rs12913832:GA are expected to have brown eyes. The purpose of the study presented here was to identify new variants in known pigmentary genes, which may explain brown eye colour formation in individuals with the rs12913832:GG genotype. Identification of these variants could help increase the understanding of eye colour biology, and increase the accuracy for DNA based eye colour prediction. Genes and regulatory regions surrounding the pigmentary genes SLC24A4, TYRP1, SLC24A5, IRF4, TYR, and SLC45A2, as well as the upstream region of OCA2 within HERC2 were investigated with massively parallel sequencing (MPS) in 40 rs12913832:GG individuals with different eye colours that were determined by quantitative eye colour measurements

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