Puigserver P, Wu Z, Park C W, Graves R, Wright M, Spiegelman B M
Dana-Farber Cancer Institute and Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Cell. 1998 Mar 20;92(6):829-39. doi: 10.1016/s0092-8674(00)81410-5.
Adaptive thermogenesis is an important component of energy homeostasis and a metabolic defense against obesity. We have cloned a novel transcriptional coactivator of nuclear receptors, termed PGC-1, from a brown fat cDNA library. PGC-1 mRNA expression is dramatically elevated upon cold exposure of mice in both brown fat and skeletal muscle, key thermogenic tissues. PGC-1 greatly increases the transcriptional activity of PPARgamma and the thyroid hormone receptor on the uncoupling protein (UCP-1) promoter. Ectopic expression of PGC-1 in white adipose cells activates expression of UCP-1 and key mitochondrial enzymes of the respiratory chain, and increases the cellular content of mitochondrial DNA. These results indicate that PGC-1 plays a key role in linking nuclear receptors to the transcriptional program of adaptive thermogenesis.
适应性产热是能量平衡的重要组成部分,也是抵御肥胖的一种代谢防御机制。我们从棕色脂肪cDNA文库中克隆了一种新型核受体转录共激活因子,命名为PGC-1。在小鼠经冷暴露后,棕色脂肪和骨骼肌这两个关键产热组织中PGC-1 mRNA的表达显著升高。PGC-1极大地增强了过氧化物酶体增殖物激活受体γ(PPARγ)和甲状腺激素受体对解偶联蛋白(UCP-1)启动子的转录活性。PGC-1在白色脂肪细胞中的异位表达激活了UCP-1和呼吸链关键线粒体酶的表达,并增加了线粒体DNA的细胞含量。这些结果表明,PGC-1在将核受体与适应性产热的转录程序联系起来方面起着关键作用。