학술논문

Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity
Document Type
article
Source
Science. 373(6550)
Subject
Prevention
Human Genome
Nutrition
Genetics
Obesity
Aetiology
2.1 Biological and endogenous factors
Metabolic and endocrine
Stroke
Oral and gastrointestinal
Cardiovascular
Animals
Body Mass Index
Exome
Genetic Variation
Humans
Mice
Mice
Knockout
Receptors
G-Protein-Coupled
Sequence Analysis
DNA
Weight Gain
Regeneron Genetics Center
DiscovEHR Collaboration
General Science & Technology
Language
Abstract
Large-scale human exome sequencing can identify rare protein-coding variants with a large impact on complex traits such as body adiposity. We sequenced the exomes of 645,626 individuals from the United Kingdom, the United States, and Mexico and estimated associations of rare coding variants with body mass index (BMI). We identified 16 genes with an exome-wide significant association with BMI, including those encoding five brain-expressed G protein-coupled receptors (CALCR, MC4R, GIPR, GPR151, and GPR75). Protein-truncating variants in GPR75 were observed in ~4/10,000 sequenced individuals and were associated with 1.8 kilograms per square meter lower BMI and 54% lower odds of obesity in the heterozygous state. Knock out of Gpr75 in mice resulted in resistance to weight gain and improved glycemic control in a high-fat diet model. Inhibition of GPR75 may provide a therapeutic strategy for obesity.