Liu Q, Bai C, Chen F, Wang R, MacDonald T, Gu M, Zhang Q, Morsy M A, Caskey C T
Department of Human Genetics, Merck Research Laboratories, West Point, PA 19486, USA.
Gene. 1998 Jan 19;207(1):1-7. doi: 10.1016/s0378-1119(97)00596-9.
We identified and partially characterized another member of the uncoupling protein termed UCP3. Human and mouse UCP3 protein sequences are 86% identical to each other, and 73% and 59% identical to UCP2 and UCP1, respectively. Expression of human UCP3 in yeast resulted in a drastic decrease of mitochondria membrane potential. Northern analysis showed that UCP3 was highly expressed in skeletal muscle in human, rat, and mouse. Mapping of UCP3 placed it to the same chromosomal region of UCP2 in both human and mouse, a region that is linked to obesity and hyperinsulinemia. Furthermore, adenovirus-mediated leptin expression in obese ob/ob mice led to increased expression of UCP3 in skeletal muscle. The data indicate that UCP3 encodes a muscle-specific uncoupling protein that may play an important role in the regulation of energy expenditure and development of obesity.
我们鉴定并部分表征了解偶联蛋白的另一个成员,称为UCP3。人和小鼠的UCP3蛋白序列彼此具有86%的同一性,分别与UCP2和UCP1具有73%和59%的同一性。人UCP3在酵母中的表达导致线粒体膜电位急剧下降。Northern分析表明,UCP3在人、大鼠和小鼠的骨骼肌中高度表达。UCP3的定位显示它在人和小鼠中都位于与UCP2相同的染色体区域,该区域与肥胖症和高胰岛素血症有关。此外,腺病毒介导的瘦素在肥胖的ob/ob小鼠中的表达导致骨骼肌中UCP3的表达增加。数据表明,UCP3编码一种肌肉特异性解偶联蛋白,可能在能量消耗调节和肥胖症发展中起重要作用。