학술논문

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
Document Type
article
Source
Nature communications. 5(1)
Subject
Chromosomes
Human
Pair 8
Chromosomes
Human
Pair 11
Humans
Hypercholesterolemia
Hypertriglyceridemia
Obesity
Genetic Predisposition to Disease
Lipoprotein Lipase
Protein Kinases
Apolipoproteins A
Logistic Models
Case-Control Studies
Genotype
Haplotypes
Polymorphism
Single Nucleotide
Adult
Middle Aged
Indians
North American
European Continental Ancestry Group
Mexico
Female
Male
Dyslipidemias
Genome-Wide Association Study
Young Adult
Nuclear Receptor Subfamily 1
Group F
Member 1
Apolipoprotein A-V
Language
Abstract
Dyslipidemia and obesity are especially prevalent in populations with Amerindian backgrounds, such as Mexican-Americans, which predispose these populations to cardiovascular disease. Here we design an approach, known as the cross-population allele screen (CPAS), which we conduct prior to a genome-wide association study (GWAS) in 19,273 Europeans and Mexicans, in order to identify Amerindian risk genes in Mexicans. Utilizing CPAS to restrict the GWAS input variants to only those differing in frequency between the two populations, we identify novel Amerindian lipid genes, receptor-related orphan receptor alpha (RORA) and salt-inducible kinase 3 (SIK3), and three loci previously unassociated with dyslipidemia or obesity. We also detect lipoprotein lipase (LPL) and apolipoprotein A5 (APOA5) harbouring specific Amerindian signatures of risk variants and haplotypes. Notably, we observe that SIK3 and one novel lipid locus underwent positive selection in Mexicans. Furthermore, after a high-fat meal, the SIK3 risk variant carriers display high triglyceride levels. These findings suggest that Amerindian-specific genetic architecture leads to a higher incidence of dyslipidemia and obesity in modern Mexicans.