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Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations
Univ Toronto, Dept Anthropol, Hlth Sci Complex,Room 352, Mississauga, ON L5L 1C6, Canada.
Univ La Laguna, Res Unit, Hosp Univ NS de Candelaria, Santa Cruz De Tenerife, Spain;Univ La Laguna, Genom & Hlth Grp, Dept Biochem Microbiol Cell Biol & Genet, Tenerife, Spain.
Univ Penn, Dept Genet, Perelman Sch Med, Philadelphia, PA 19104 USA.
NCI, Lab Translat Genom, Div Canc Epidemiol & Genet, NIH, Bethesda, MD 20892 USA.
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2019 (English)In: BMC Genetics, ISSN 1471-2156, E-ISSN 1471-2156, Vol. 20, article id 59Article in journal (Refereed) Published
Abstract [en]

Background: Association studies in recently admixed populations are extremely useful to identify the genetic architecture of pigmentation, due to their high genotypic and phenotypic variation. However, to date only four Genome-Wide Association Studies (GWAS) have been carried out in these populations.

Results: We present a GWAS of skin pigmentation in an admixed sample from Cuba (N=762). Additionally, we conducted a meta-analysis including the Cuban sample, and admixed samples from Cape Verde, Puerto Rico and African-Americans from San Francisco. This meta-analysis is one of the largest efforts so far to characterize the genetic basis of skin pigmentation in admixed populations (N=2,104). We identified five genome-wide significant regions in the meta-analysis, and explored if the markers observed in these regions are associated with the expression of relevant pigmentary genes in human melanocyte cultures. In three of the regions identified in the meta-analysis (SLC24A5, SLC45A2, and GRM5/TYR), the association seems to be driven by non-synonymous variants (rs1426654, rs16891982, and rs1042602, respectively). The rs16891982 polymorphism is strongly associated with the expression of the SLC45A2 gene. In the GRM5/TYR region, in addition to the rs1042602 non-synonymous SNP located on the TYR gene, variants located in the nearby GRM5 gene have an independent effect on pigmentation, possibly through regulation of gene expression of the TYR gene. We also replicated an association recently described near the MFSD12 gene on chromosome 19 (lead variant rs112332856). Additionally, our analyses support the presence of multiple signals in the OCA2/HERC2/APBA2 region on chromosome 15. A clear causal candidate is the HERC2 intronic variant rs12913832, which has a profound influence on OCA2 expression. This variant has pleiotropic effects on eye, hair, and skin pigmentation. However, conditional and haplotype-based analyses indicate the presence of other variants with independent effects on melanin levels in OCA2 and APBA2. Finally, a follow-up of genome-wide signals identified in a recent GWAS for tanning response indicates that there is a substantial overlap in the genetic factors influencing skin pigmentation and tanning response.

Conclusions: Our meta-analysis of skin pigmentation GWAS in recently admixed populations provides new insights about the genetic architecture of this complex trait.

Place, publisher, year, edition, pages
BMC , 2019. Vol. 20, article id 59
Keywords [en]
Skin pigmentation, Genome-wide association study, Admixed populations, Meta-analysis, Complex trait, Gene expression, Haplotype
National Category
Medical Genetics
Identifiers
URN: urn:nbn:se:uu:diva-390776DOI: 10.1186/s12863-019-0765-5ISI: 000475919200001PubMedID: 31315583OAI: oai:DiVA.org:uu-390776DiVA, id: diva2:1343491
Funder
EU, Horizon 2020, AC15/00015Available from: 2019-08-16 Created: 2019-08-16 Last updated: 2019-08-16Bibliographically approved

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