Variations in the uncoupling protein-3 gene are associated with specific obesity phenotypes

Eur J Endocrinol. 2008 May;158(5):669-76. doi: 10.1530/EJE-07-0834.

Abstract

Objective: Uncoupling protein 3 (UCP-3) uncouples oxidative metabolism from ATP synthesis, resulting in the production of heat instead of energy storage. Single nucleotide polymorphisms (SNPs) in UCP-3 might result in a reduced function or expression of UCP-3 and therefore lead to an increased capacity to store energy as fat.

Design: We conducted a population-based, cross-sectional single-center study among 400 Dutch men between 40 and 80 years.

Methods: Seven SNPs in the UCP-3 gene were genotyped by means of an allele-specific real-time TaqMan PCR. Linear regression analyses were performed to examine the independent effects of these SNPs on obesity phenotypes.

Results: We found a significant association between homozygosity for the minor allele of rs647126, rs1685356, and rs2075577 and an increase in body mass index (BMI; P=0.033, P=0.016, and P=0.019 respectively). Heterozygosity for rs1685354 was associated with a significant decrease in visceral fat mass (P=0.030).

Conclusions: Our results suggest that genetic variations in the UCP-3 gene are associated with an increase in BMI. A plausible mechanism by which these SNPs lead to an increase in BMI is that due to these SNPs, the UCP-3 activity might be decreased. As a result, uncoupling activity may also decrease, which will lead to an increase in body weight and BMI.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adipose Tissue / physiology
  • Adult
  • Aged
  • Aged, 80 and over
  • Body Mass Index
  • Cross-Sectional Studies
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Variation*
  • Genotype
  • Humans
  • Ion Channels / genetics*
  • Ion Channels / metabolism
  • Male
  • Middle Aged
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • Netherlands / epidemiology
  • Obesity / genetics*
  • Obesity / metabolism
  • Obesity / physiopathology*
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Uncoupling Protein 3

Substances

  • Ion Channels
  • Mitochondrial Proteins
  • UCP3 protein, human
  • Uncoupling Protein 3
  • Adenosine Triphosphate