Mendelson S C, Morrison C F, McAllister J, Paterson J M, Dobson S P, Mulderry P K, Quinn J P
MRC Brain Metabolism Unit, Royal Edinburgh Hospital, U.K.
Neuroscience. 1995 Apr;65(3):837-47. doi: 10.1016/0306-4522(94)00554-i.
The rat preprotachykinin-A promoter, which is able to direct reporter gene expression in adult dorsal root ganglia neurons grown in culture, has no detectable activity in HeLa and PC12 cells. DNAase 1 footprinting and electrophoretic mobility shift analyses with HeLa nuclear extract indicated the presence of a protein complex binding to a region of the rat preprotachykinn-A gene promoter between the TATA box and the major transcriptional start site. We demonstrate that the sequence of the preprotachykinin-A promoter spanning nucleotides -47 to +92 functions to repress reporter gene expression in HeLa and PC12 cells but not in adult rat dorsal root ganglia grown in culture, and that this repression is correlated with a protein(s) binding to the element between the TATA box and major transcription initiation site. These results indicate that the tissue-specific expression of the preprotachykinin-A gene could require the interaction of both positive and negative regulatory DNA elements.
大鼠前速激肽原A启动子能够指导培养的成年背根神经节神经元中报告基因的表达,但在HeLa细胞和PC12细胞中未检测到活性。用HeLa细胞核提取物进行的DNA酶I足迹分析和电泳迁移率变动分析表明,存在一种蛋白质复合物,它与大鼠前速激肽原A基因启动子中位于TATA盒和主要转录起始位点之间的区域结合。我们证明,前速激肽原A启动子跨越核苷酸-47至+92的序列可抑制HeLa细胞和PC12细胞中报告基因的表达,但对培养的成年大鼠背根神经节无此作用,并且这种抑制作用与一种或多种与TATA盒和主要转录起始位点之间的元件结合的蛋白质相关。这些结果表明,前速激肽原A基因的组织特异性表达可能需要正负调控DNA元件的相互作用。