4.7 Article

Further insight into the global variability of the OCA2-HERC2 locus for human pigmentation from multiallelic markers

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-01940-w

Keywords

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Funding

  1. University Center of Legal Medicine of the University Hospital of Lausanne
  2. Swiss National Foundation [N 310030_184705]
  3. Swiss National Science Foundation (SNF) [310030_184705] Funding Source: Swiss National Science Foundation (SNF)

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The study analyzed 11 microsatellites to examine haplotype structures and allelic associations in the OCA2-HERC2 region, revealing significant differences in allele frequency among European, East Asian, and African populations. Haplotypes carrying specific alleles were found to be associated with predicted eye colors and showed high frequency in certain populations. This highlights the informative nature of multiallelic markers and supports the use of microsatellites for identifying causative variants with similar genetic features and history.
The OCA2-HERC2 locus is responsible for the greatest proportion of eye color variation in humans. Numerous studies extensively described both functional SNPs and associated patterns of variation over this region. The goal of our study is to examine how these haplotype structures and allelic associations vary when highly variable markers such as microsatellites are used. Eleven microsatellites spanning 357 Kb of OCA2-HERC2 genes are analyzed in 3029 individuals from worldwide populations. We found that several markers display large differences in allele frequency (10% to 35% difference) among Europeans, East Asians and Africans. In Europe, the alleles showing increased frequency can also discriminate individuals with (IrisPlex) predicted blue and brown eyes. Distinct haplotypes are identified around the variants C and T of the functional SNP rs12913832 (associated to blue eyes), with linkage disequilibrium r(2) values significant up to 237 Kb. The haplotype carrying the allele rs12913832 C has high frequency (76%) in blue eye predicted individuals (30% in brown eye predicted individuals), while the haplotype associated to the allele rs12913832 T is restricted to brown eye predicted individuals. Finally, homozygosity values reach levels of 91% near rs12913832. Odds ratios show values of 4.2, 7.4 and 10.4 for four markers around rs12913832 and 7.1 for their core haplotype. Hence, this study provides an example on the informativeness of multiallelic markers that, despite their current limited potential contribution to forensic eye color prediction, supports the use of microsatellites for identifying causing variants showing similar genetic features and history.

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