Liu H C, Shen J T, Augustin L B, Ko J L, Loh H H
Department of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
J Biol Chem. 1999 Aug 13;274(33):23617-26. doi: 10.1074/jbc.274.33.23617.
Three major types of opioid receptors, mu (MOR), delta (DOR), and kappa (KOR), have been cloned and characterized. Each opioid receptor exhibits a distinct pharmacological profile as well as a distinct pattern of temporal and spatial expression in the brain, suggesting the critical role of transcription regulatory elements and their associated factors. Here, we report the identification of a minimum core promoter, in the 5'-flanking region of the mouse DOR gene, containing an E box and a GC box that are crucial for DOR promoter activity in NS20Y cells, a DOR-expressing mouse neuronal cell line. In vitro protein-DNA binding assays and in vivo transient transfection assays indicated that members of both the upstream stimulatory factor and Sp families of transcription factors bound to and trans-activated the DOR promoter via the E box and GC box, respectively. Furthermore, functional and physical interactions between these factors were critical for the basal as well as maximum promoter activity of the DOR gene. Thus, the distinct developmental emergence and brain regional distribution of the delta opioid receptor appear to be controlled, at least in part, by these two regulatory elements and their associated factors.
三种主要类型的阿片受体,即μ(MOR)、δ(DOR)和κ(KOR),已被克隆并鉴定。每种阿片受体都表现出独特的药理学特征以及在大脑中独特的时空表达模式,这表明转录调控元件及其相关因子起着关键作用。在此,我们报告在小鼠DOR基因的5'侧翼区域鉴定出一个最小核心启动子,其包含一个E盒和一个GC盒,这两个元件对NS20Y细胞(一种表达DOR的小鼠神经元细胞系)中的DOR启动子活性至关重要。体外蛋白质-DNA结合试验和体内瞬时转染试验表明,转录因子上游刺激因子家族和Sp家族的成员分别通过E盒和GC盒与DOR启动子结合并反式激活该启动子。此外,这些因子之间的功能和物理相互作用对于DOR基因的基础以及最大启动子活性至关重要。因此,δ阿片受体独特的发育出现和脑区分布似乎至少部分受这两个调控元件及其相关因子的控制。