Literature DB >> 27455349

A thrifty variant in CREBRF strongly influences body mass index in Samoans.

Ryan L Minster1, Nicola L Hawley2, Chi-Ting Su1, Guangyun Sun3, Erin E Kershaw4, Hong Cheng3, Olive D Buhule5, Jerome Lin1, Muagututi'a Sefuiva Reupena6, Satupa'itea Viali7, John Tuitele8, Take Naseri9, Zsolt Urban1, Ranjan Deka3, Daniel E Weeks1,5, Stephen T McGarvey10,11.   

Abstract

Samoans are a unique founder population with a high prevalence of obesity, making them well suited for identifying new genetic contributors to obesity. We conducted a genome-wide association study (GWAS) in 3,072 Samoans, discovered a variant, rs12513649, strongly associated with body mass index (BMI) (P = 5.3 × 10(-14)), and replicated the association in 2,102 additional Samoans (P = 1.2 × 10(-9)). Targeted sequencing identified a strongly associated missense variant, rs373863828 (p.Arg457Gln), in CREBRF (meta P = 1.4 × 10(-20)). Although this variant is extremely rare in other populations, it is common in Samoans (frequency of 0.259), with an effect size much larger than that of any other known common BMI risk variant (1.36-1.45 kg/m(2) per copy of the risk-associated allele). In comparison to wild-type CREBRF, the Arg457Gln variant when overexpressed selectively decreased energy use and increased fat storage in an adipocyte cell model. These data, in combination with evidence of positive selection of the allele encoding p.Arg457Gln, support a 'thrifty' variant hypothesis as a factor in human obesity.

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Year:  2016        PMID: 27455349      PMCID: PMC5069069          DOI: 10.1038/ng.3620

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  62 in total

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