Unraveling the genetics of human obesity.

Abstract

The use of modern molecular biology tools in deciphering the perturbed biochemistry and physiology underlying the obese state has proven invaluable. Identifying the hypothalamic leptin/melanocortin pathway as critical in many cases of monogenic obesity has permitted targeted, hypothesis-driven experiments to be performed, and has implicated new candidates as causative for previously uncharacterized clinical cases of obesity. Meanwhile, the effects of mutations in the melanocortin-4 receptor gene, for which the obese phenotype varies in the degree of severity among individuals, are now thought to be influenced by one's environmental surroundings. Molecular approaches have revealed that syndromes (Prader-Willi and Bardet-Biedl) previously assumed to be controlled by a single gene are, conversely, regulated by multiple elements. Finally, the application of comprehensive profiling technologies coupled with creative statistical analyses has revealed that interactions between genetic and environmental factors are responsible for the common obesity currently challenging many Westernized societies. As such, an improved understanding of the different "types" of obesity not only permits the development of potential therapies, but also proposes novel and often unexpected directions in deciphering the dysfunctional state of obesity.

• Authors: David M Mutch, Karine Clément
• Journal: PLoS genetics (PLoS Genet) Vol. 2 Issue 12 Pg. e188 (Dec 29 2006) ISSN: 1553-7404 [Electronic] United States
• PMID: 17196040 (Publication Type: Journal Article, Review)

Topics

• Animals
• Chromosome Mapping
• Environment
• Gene Expression Profiling
• Humans
• Hypothalamus (physiopathology)
• Mutation
• Obesity (genetics, physiopathology)
• Phenotype
• Syndrome