Abstract

Skin pigmentation is one of the most prominent and variable phenotypes in humans. We compared the alleles of 163 SNPs and indels from the Human Pigmentation (HuPi) AmpliSeq™ Custom panel, and biogeographic ancestry with the quantitative skin pigmentation levels on the upper arm, lower arm, and forehead of 299 Pakistani individuals from three subpopulations: Baloch, Pashtun, and Punjabi. The biogeographic ancestry of each individual was estimated using the Precision ID Ancestry Panel. All individuals were mainly of mixed South-Central Asian and European ancestry. However, the Baloch individuals also had an average proportion of Sub-Saharan African ancestry of approximately 10%, whereas it was <1% in the Punjabi and Pashtun individuals. The pairwise genetic distances between the Pashtun, Punjabi, and Baloch subpopulations based on the ancestry markers were statistically significantly different. Individuals from the Pashtun subpopulation had statistically significantly lower skin pigmentation than individuals from the Punjabi and Baloch subpopulations (p < 0.05). The proportions of European and Sub-Saharan African ancestry and five SNPs (rs1042602, rs10831496, rs1426654, rs16891982, and rs12913832) were statistically significantly associated with skin pigmentation at either the upper arm, lower arm or forehead in the Pakistani population after correction for multiple testing (p < 10−3). A model based on four of these SNPs (rs1426654, rs1042602, rs16891982, and rs12913832) explained 33% of the upper arm skin pigmentation. The four SNPs and the proportions of European and Sub-Saharan African ancestry explained 37% of the upper arm skin pigmentation. Our results indicate that the four likely causative SNPs, rs1426654, rs1042602, rs16891982, and rs12913832 located in SLC24A5, TYR, SLC45A2, and HERC2, respectively, are essential for skin color variation in the admixed Pakistani subpopulations.

Highlights

  • Human pigmentation is one of the most variable externally visible characteristics (EVCs)

  • The genetics of human pigmentation is a field of great interest in forensic genetics because it offers a prediction of three prominent EVCs: hair, eye, and skin color [4,5]

  • The pairwise genetic distances calculated among the three subpopulations were statistically significantly different (Supplementary Table S3)

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Summary

Introduction

Human pigmentation is one of the most variable externally visible characteristics (EVCs). The genetics of human pigmentation is a field of great interest in forensic genetics because it offers a prediction of three prominent EVCs: hair, eye, and skin color [4,5]. Skin pigmentation is strongly associated with biogeographic ancestry [6]. Prediction of the biogeographic ancestry may indicate skin pigmentation of the individual. Skin color prediction based on the assumption that biogeographic ancestry and skin color are well correlated only offers an indirect prediction, and the assumption is not necessarily true in admixed populations [8,9].

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