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Variation in body fat distribution contributes to the metabolic sequelae of obesity. The genetic determinants of body fat distribution are poorly understood. The goal of this study was to gain new insights into the underlying genetics of body fat distribution by conducting sample-size-weighted fixed-effects genome-wide association meta-analyses in up to 9,594 women and 8,738 men of European, African, Hispanic and Chinese ancestry, with and without sex stratification, for six traits associated with ectopic fat (hereinafter referred to as ectopic-fat traits). In total, we identified seven new loci associated with ectopic-fat traits (ATXN1, UBE2E2, EBF1, RREB1, GSDMB, GRAMD3 and ENSA; P < 5 × 10-8; false discovery rate < 1%). Functional analysis of these genes showed that loss of function of either Atxn1 or Ube2e2 in primary mouse adipose progenitor cells impaired adipocyte differentiation, suggesting physiological roles for ATXN1 and UBE2E2 in adipogenesis. Future studies are necessary to further explore the mechanisms by which these genes affect adipocyte biology and how their perturbations contribute to systemic metabolic disease.

Original publication

DOI

10.1038/ng.3738

Type

Journal article

Journal

Nature genetics

Publication Date

01/2017

Volume

49

Pages

125 - 130

Addresses

NHLBI's Framingham Heart Study, Framingham, Massachusetts, USA.

Keywords

Adipocytes, Animals, Mice, Inbred C57BL, Humans, Mice, Obesity, Genetic Predisposition to Disease, Genetic Markers, Cohort Studies, Cell Differentiation, Phenotype, Polymorphism, Single Nucleotide, Ethnic Groups, Female, Male, Body Fat Distribution, Genome-Wide Association Study, Genetic Loci