Rivera-Gines Aida, Cook Ryan J, Loh Horace H, Ko Jane L
Department of Biology, Seton Hall University, South Orange, NJ 07079, USA.
Biochem Biophys Res Commun. 2006 Jun 23;345(1):530-7. doi: 10.1016/j.bbrc.2006.04.117. Epub 2006 May 2.
The proximal promoter of mouse mu-opioid receptor (MOR) gene is the dominant promoter for directing MOR-1 gene expression in brain. Sp1/Sp3 (Sps) and poly(C) binding protein 1 (PCBP) bind to a cis-element of MOR proximal promoter. Functional interaction between Sps and PCBP and their individual roles on MOR proximal core promoter were investigated using SL2 cells, devoid of Sps and PCBP. Each factor contributed differentially to the promoter, with a rank order of activity Sp1>Sp3>PCBP. Functional analysis suggested the interplay of Sps and PCBP in an additive manner. The in vivo binding of individual Sps or PCBP to MOR proximal promoter was demonstrated using chromatin immunoprecipitation (ChIP). Re-ChIP assays further suggested simultaneous bindings of Sps and PCBP to the proximal promoter, indicating physiologically relevant communication between Sps and PCBP. Collectively, results documented that a functional coordination between Sps and PCBP contributed to cell-specific MOR gene expression.
小鼠μ-阿片受体(MOR)基因的近端启动子是指导MOR-1基因在大脑中表达的主要启动子。Sp1/Sp3(Sps)和多聚(C)结合蛋白1(PCBP)与MOR近端启动子的一个顺式元件结合。利用缺乏Sps和PCBP的SL2细胞,研究了Sps与PCBP之间的功能相互作用及其在MOR近端核心启动子上的各自作用。每个因子对启动子的贡献不同,活性顺序为Sp1>Sp3>PCBP。功能分析表明Sps和PCBP以累加方式相互作用。使用染色质免疫沉淀(ChIP)证明了单个Sps或PCBP与MOR近端启动子的体内结合。再免疫沉淀分析进一步表明Sps和PCBP同时与近端启动子结合,表明Sps和PCBP之间存在生理相关的相互作用。总体而言,结果证明Sps和PCBP之间的功能协调有助于细胞特异性MOR基因表达。