[No authors listed]
Vitamin B12 is an important cofactor in one-carbon metabolism whose dysregulation is associated with various clinical conditions. Indians have a high prevalence of B12 deficiency but little is known about the genetic determinants of circulating B12 concentrations in Indians. We performed a genome-wide association study in 1001 healthy participants in the Pune Maternal Nutrition Study replication studies in 3418 individuals from other Indian cohorts and by meta-analysis identified new variants, rs3760775 (Pâ=â1.2âÃâ10-23) and rs78060698 (Pâ=â8.3âÃâ10-17) in FUT6 to be associated with circulating B12 concentrations. Although in-silico analysis replicated both variants in Europeans, differences in the effect allele frequency, effect size and the linkage disequilibrium structure of credible set variants with the reported variants suggest population-specific characteristics in this region. We replicated previously reported variants rs602662, rs601338 in FUT2, rs3760776, rs708686 in FUT6, rs34324219 in TCN1 (all Pâ<â5âÃâ10-8), rs1131603 in TCN2 (Pâ=â3.4âÃâ10-5), rs12780845 in CUBN (Pâ=â3.0âÃâ10-3) and rs2270655 in MMAA (Pâ=â2.0âÃâ10-3). Circulating B12 concentrations in the and Parthenon study showed a significant decline with increasing age (Pâ<â0.001), however, the genetic contribution to B12 concentrations remained constant. Luciferase reporter and electrophoretic-mobility shift assay for the FUT6 variant rs78060698 using HepG2 cell line demonstrated strong allele-specific promoter and enhancer activity and differential binding of HNF4α, a key regulator of expression of various fucosyltransferases. Hence, the rs78060698 variant, through regulation of fucosylation may control intestinal host-microbial interaction which could influence B12 concentrations. Our results suggest that in addition to established genetic variants, population-specific variants are important in determining plasma B12 concentrations. © The Author 2017. Published by Oxford University Press.
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