A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia
Adhikari KPapers in this archive, Mendoza-Revilla JPapers in this archive, Sohail APapers in this archive, Fuentes-Guajardo MPapers in this archive, Lampert JPapers in this archive, Chacón-Duque JCPapers in this archive, Hurtado MPapers in this archive, Villegas VPapers in this archive, Granja VPapers in this archive, Acuña-Alonzo VPapers in this archive, Jaramillo CPapers in this archive, Arias WPapers in this archive, Lozano RBPapers in this archive, Everardo PPapers in this archive, Gómez-Valdés JPapers in this archive, Villamil-Ramírez HPapers in this archive, Silva de Cerqueira CCPapers in this archive, Hunemeier TPapers in this archive, Ramallo VPapers in this archive, Schuler-Faccini LPapers in this archive, Salzano FMPapers in this archive, Gonzalez-José RPapers in this archive, Bortolini MCPapers in this archive, Canizales-Quinteros SPapers in this archive, Gallo CPapers in this archive, Poletti GPapers in this archive, Bedoya GPapers in this archive, Rothhammer FPapers in this archive, Tobin DJPapers in this archive, Fumagalli MPapers in this archive, Balding DPapers in this archive, Ruiz-Linares APapers in this archive
Abstract
We report a genome-wide association scan in >6,000 Latin Americans for pigmentation of skin and eyes. We found eighteen signals of association at twelve genomic regions. These include one novel locus for skin pigmentation (in 10q26) and three novel loci for eye pigmentation (in 1q32, 20q13 and 22q12). We demonstrate the presence of multiple independent signals of association in the 11q14 and 15q13 regions (comprising the GRM5/TYR and HERC2/OCA2 genes, respectively) and several epistatic interactions among independently associated alleles. Strongest association with skin pigmentation at 19p13 was observed for an Y182H missense variant (common only in East Asians and Native Americans) in MFSD12, a gene recently associated with skin pigmentation in Africans. We show that the frequency of the derived allele at Y182H is significantly correlated with lower solar radiation intensity in East Asia and infer that MFSD12 was under selection in East Asians, probably after their split from Europeans.
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