Cloning and Characterization of an Uncoupling Protein Homolog: A Potential Molecular Mediator of Human Thermogenesis
Ruth E. Gimeno, Marlene Dembski, Xun Weng et al.
Research Article — Peer-Reviewed Source
Original research published by Gimeno et al. in Diabetes. Redistributed under Open Access — see publisher for license terms. MedTech Research Group provides these references for informational purposes. We do not conduct original research. All studies are the work of their respective authors and institutions.
We have identified a novel cDNA encoding a protein highly homologous to the mammalian brown fat uncoupling protein (UCP). Unlike the known UCP, which is expressed specifically in brown adipose tissue, the UCP homolog (UCPH) mRNA is expressed in a variety of tissues, with predominant expression in human white adipose tissue and skeletal muscle. In the white adipose tissue of ob/ob and db/db mice, the UCPH transcript is induced approximately fivefold relative to lean littermate controls. Expression of murine UCPH in yeast results in growth inhibition under conditions that require aerobic respiration, but does not affect growth under anaerobic conditions. Furthermore, UCPH expression in yeast causes a decrease in the mitochondrial membrane potential, as judged by staining with the potential-sensitive dye DiOC6. These observations suggest that UCPH, like UCP, uncouples oxidative phosphorylation. The possibility that the UCPH protein is an important mediator of human thermogenesis is discussed.
Full text is available at the publisher.
Read at Publisher| DOI | 10.2337/diab.46.5.900 |
| Journal | Diabetes |
| Year | 1997 |
| Authors | Ruth E. Gimeno, Marlene Dembski, Xun Weng, Nanhua Deng, Andrew W. Shyjan, Carlos J. Gimeno, François Iris, Stephen J. Ellis, Elizabeth A. Woolf, Louis A. Tartaglia |
| License | Open Access — see publisher for license terms |
| Citations | 480 |