Uncoupling protein-2: a novel gene linked to obesity and hyperinsulinemia

A mitochondrial protein called uncoupling protein (UCP1) plays an important role in generating heat and burning calories by creating a pathway that allows dissipation of the proton electrochemical gradient across the inner mitochondrial membrane in brown adipose tissue, without coupling to any other energy-consuming process1. This pathway has been implicated in the regulation of body temperature, body composition and glucose metabolism2. However, UCP1-containing brown adipose tissue is unlikely to be involved in weight regulation in adult large-size animals and humans living in a thermoneutral environment (one where an animal does not have to increase oxygen consumption or energy expenditure to lose or gain heat to maintain body temperature), as there is little brown adipose tissue present3. We now report the discovery of a gene that codes for a novel uncoupling protein, designated UCP2, which has 59% amino-acid identity to UCP1, and describe properties consistent with a role in diabetes and obesity. In comparison with UCP1, UCP2 has a greater effect on mitochondrial membrane potential when expressed in yeast. Compared to UCP1, the gene is widely expressed in adult human tissues, including tissues rich in macrophages, and it is upregulated in white fat in response to fat feeding. Finally, UCP2 maps to regions of human chromosome 11 and mouse chromosome 7 that have been linked to hyperinsulinaemia and obesity. Our findings suggest that UCP2 has a unique role in energy balance, body weight regulation and thermoregulation and their responses to inflammatory stimuli.

[1]  Martin D. Brand,et al.  Body mass dependence of H+ leak in mitochondria and its relevance to metabolic rate , 1993, Nature.

[2]  S. Horvat,et al.  Interval mapping of high growth (hg), a major locus that increases weight gain in mice. , 1995, Genetics.

[3]  L. Casteilla,et al.  A sequence related to a DNA recognition element is essential for the inhibition by nucleotides of proton transport through the mitochondrial uncoupling protein. , 1994, The EMBO journal.

[4]  M. Feinglos,et al.  The role of motor activity in diet-induced obesity in C57BL/6J mice , 1996, Physiology & Behavior.

[5]  M. James,et al.  Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq , 1994, Nature.

[6]  D. Nicholls,et al.  Thermogenic mechanisms in brown fat. , 1984, Physiological reviews.

[7]  J. Neel Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"? , 1962, American journal of human genetics.

[8]  K. Svenson,et al.  Identification of four chromosomal loci determining obesity in a multifactorial mouse model. , 1995, The Journal of clinical investigation.

[9]  M. Brand,et al.  Causes of differences in respiration rate of hepatocytes from mammals of different body mass. , 1995, The American journal of physiology.

[10]  B. Cannon,et al.  Chapter 17 The uncoupling protein thermogenin and mitochondrial thermogenesis , 1992 .

[11]  M. Brand,et al.  Evolution of energy metabolism. Proton permeability of the inner membrane of liver mitochondria is greater in a mammal than in a reptile. , 1991, The Biochemical journal.

[12]  M. Klingenberg,et al.  The reconstituted ADP/ATP carrier can mediate H+ transport by free fatty acids, which is further stimulated by mersalyl. , 1994, The Journal of biological chemistry.

[13]  Michael J. Stock,et al.  A role for brown adipose tissue in diet-induced thermogenesis , 1979, Nature.

[14]  G. Garruti,et al.  Analysis of uncoupling protein and its mRNA in adipose tissue deposits of adult humans. , 1992, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.

[15]  S. Kingsmore,et al.  Glycogen synthase: a putative locus for diet-induced hyperglycemia. , 1994, The Journal of clinical investigation.

[16]  S. Prieto,et al.  Activation by ATP of a proton-conducting pathway in yeast mitochondria. , 1992, European journal of biochemistry.

[17]  B. Taylor,et al.  Detection of obesity QTLs on mouse chromosomes 1 and 7 by selective DNA pooling. , 1996, Genomics.

[18]  M. Seldin,et al.  Human/mouse homology relationships. , 1996, Genomics.

[19]  K. Clément,et al.  Genetic Variation in the β3-Adrenergic Receptor and an Increased Capacity to Gain Weight in Patients with Morbid Obesity , 1995 .

[20]  J. Rodin,et al.  Differential effects of fat and sucrose on the development of obesity and diabetes in C57BL/6J and A/J mice. , 1995, Metabolism: clinical and experimental.

[21]  E. Cerasi,et al.  DIABETES MELLITUS , 1924, Nihon rinsho. Japanese journal of clinical medicine.

[22]  M. Feinglos,et al.  Diet-Induced Type II Diabetes in C57BL/6J Mice , 1988, Diabetes.

[23]  J. Himms-Hagen,et al.  Brown adipose tissue thermogenesis: interdisciplinary studies , 1990, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[24]  D. West,et al.  Dietary obesity linked to genetic loci on chromosomes 9 and 15 in a polygenic mouse model. , 1994, The Journal of clinical investigation.

[25]  C. Bouchard,et al.  DNA polymorphism in the uncoupling protein (UCP) gene and human body fat. , 1994, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.