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The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent
- Source :
- PLoS Genetics, Vol 9, Iss 11, p e1003912 (2013), PLoS Genetics
- Publication Year :
- 2013
- Publisher :
- Public Library of Science (PLoS), 2013.
-
Abstract
- Skin pigmentation is one of the most variable phenotypic traits in humans. A non-synonymous substitution (rs1426654) in the third exon of SLC24A5 accounts for lighter skin in Europeans but not in East Asians. A previous genome-wide association study carried out in a heterogeneous sample of UK immigrants of South Asian descent suggested that this gene also contributes significantly to skin pigmentation variation among South Asians. In the present study, we have quantitatively assessed skin pigmentation for a largely homogeneous cohort of 1228 individuals from the Southern region of the Indian subcontinent. Our data confirm significant association of rs1426654 SNP with skin pigmentation, explaining about 27% of total phenotypic variation in the cohort studied. Our extensive survey of the polymorphism in 1573 individuals from 54 ethnic populations across the Indian subcontinent reveals wide presence of the derived-A allele, although the frequencies vary substantially among populations. We also show that the geospatial pattern of this allele is complex, but most importantly, reflects strong influence of language, geography and demographic history of the populations. Sequencing 11.74 kb of SLC24A5 in 95 individuals worldwide reveals that the rs1426654-A alleles in South Asian and West Eurasian populations are monophyletic and occur on the background of a common haplotype that is characterized by low genetic diversity. We date the coalescence of the light skin associated allele at 22–28 KYA. Both our sequence and genome-wide genotype data confirm that this gene has been a target for positive selection among Europeans. However, the latter also shows additional evidence of selection in populations of the Middle East, Central Asia, Pakistan and North India but not in South India.<br />Author Summary Human skin color is one of the most visible aspects of human diversity. The genetic basis of pigmentation in Europeans has been understood to some extent, but our knowledge about South Asians has been restricted to a handful of studies. It has been suggested that a single nucleotide difference in SLC24A5 accounts for 25–38% European-African pigmentation differences and correlates with lighter skin. This genetic variant has also been associated with skin color variation among South Asians living in the UK. Here, we report a study based on a homogenous cohort of South India. Our results confirm that SLC24A5 plays a key role in pigmentation diversity of South Asians. Country-wide screening of the variant reveals that the light skin associated allele is widespread in the Indian subcontinent and its complex patterning is shaped by a combination of processes involving selection and demographic history of the populations. By studying the variation of SLC24A5 sequences among a diverse set of individuals, we show that the light skin associated allele in South Asians is identical by descent to that found in Europeans. Our study also provides new insights into positive selection acting on the gene and the evolutionary history of light skin in humans.
- Subjects :
- Cancer Research
lcsh:QH426-470
Demographic history
Light skin
Population genetics
Skin Pigmentation
SLC24A5
Identity by descent
Polymorphism, Single Nucleotide
Antiporters
White People
03 medical and health sciences
Asian People
Genetic variation
Genetics
Humans
Allele
10. No inequality
Molecular Biology
Genetics (clinical)
Ecology, Evolution, Behavior and Systematics
Alleles
030304 developmental biology
0303 health sciences
biology
030305 genetics & heredity
Haplotype
Genetic Variation
lcsh:Genetics
Haplotypes
Evolutionary biology
biology.protein
Research Article
Genome-Wide Association Study
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- PLoS Genetics, Vol 9, Iss 11, p e1003912 (2013), PLoS Genetics
- Accession number :
- edsair.doi.dedup.....6e49ed28b3caae8724d339bdea06d426