Silva J E, Rabelo R
Department of Medicine, Jewish General Hospital, Montreal, Quebec, Canada.
Eur J Endocrinol. 1997 Mar;136(3):251-64. doi: 10.1530/eje.0.1360251.
Uncoupling protein (UCP) is essential to the thermogenic function of brown adipose tissue (BAT). The thermogenic role of this protein is due to its capacity to uncouple oxidative phosphorylation in a regulated manner. The thermogenic potential of BAT is determined by its content of UCP. The gene encoding this protein is under complex regulation. Catecholamines, via cAMP, thyroid hormone and retinoic acid, directly stimulate the gene acting upon an upstream (-2.28/-2.49 kb) enhancer sequence, but cAMP may act upon other sequences of the gene as well. CCAAT enhancer binding proteins and peroxisome proliferation activator receptor (PPAR) gamma 2 have also been implicated in the regulation of the gene acting on discrete sequences. While the thyroid hormone response and retinoic acid response elements (TRE and RARE) have been well defined, the cAMP response elements (CRE) remain elusive. The two TREs are 27 bp apart between -2.33 kb and -2.39 kb. The synergism between cAMP and thyroid hormone seems to reside in a 39 bp sequence downstream (-2.28/-2.32 kb). The most important CRE, the RARE, a cell-specific enhancer and a putative PPAR element are all concentrated in a 90 bp regulatory element of great complexity (-2.40/-2.49 kb). Other hormones, such as insulin and glucocorticoids, and IGF-I also modulate the expression of the gene but their effects seem to be largely indirect. Understanding the regulation of the UCP gene expression may facilitate the development of interventions in obesity and related disorders.
解偶联蛋白(UCP)对于棕色脂肪组织(BAT)的产热功能至关重要。该蛋白的产热作用源于其以调控方式使氧化磷酸化解偶联的能力。BAT的产热潜能由其UCP含量决定。编码此蛋白的基因受到复杂调控。儿茶酚胺通过环磷酸腺苷(cAMP)、甲状腺激素和视黄酸,直接刺激作用于上游(-2.28 / -2.49 kb)增强子序列的基因,但cAMP也可能作用于该基因的其他序列。CCAAT增强子结合蛋白和过氧化物酶体增殖激活受体(PPAR)γ2也参与了作用于离散序列的基因调控。虽然甲状腺激素反应元件和视黄酸反应元件(TRE和RARE)已得到明确界定,但cAMP反应元件(CRE)仍不清楚。两个TRE在-2.33 kb和-2.39 kb之间相隔27 bp。cAMP与甲状腺激素之间的协同作用似乎存在于下游的一个39 bp序列(-2.28 / -2.32 kb)中。最重要的CRE、RARE、一个细胞特异性增强子和一个假定的PPAR元件都集中在一个极其复杂的90 bp调控元件(-2.40 / -2.49 kb)中。其他激素,如胰岛素、糖皮质激素和胰岛素样生长因子-I(IGF-I)也调节该基因的表达,但它们的作用似乎在很大程度上是间接的。了解UCP基因表达的调控可能有助于开发针对肥胖及相关疾病的干预措施。