Gilchrist C A, Morrison C F, Chapman K E, Harmar A J
MRC Brain Metabolism Unit, Royal Edinburgh Hospital, UK.
DNA Cell Biol. 1991 Dec;10(10):743-9. doi: 10.1089/dna.1991.10.743.
The production of substance P and the mRNA encoding its precursor (preprotachykinin, PPT) is regulated by nerve growth factor (NGF) in dorsal root ganglion (drg) neurons. To explore the mechanism by which NGF regulates the production of PPT mRNA, we have transfected PC12 cells and F11 cells with plasmids containing the bovine PPT promoter linked to the reporter gene chloramphenicol acetyltransferase (CAT). We have identified (i) functional elements within the PPT promoter which are necessary for expression in the absence of NGF and (ii) two separate regions, each of approximately 250 bp, which confer NGF responsiveness. Both regions contained a sequence element, similar to a known transcription factor binding site, which is present in several other NGF-regulated genes.
P物质及其编码前体(前速激肽原,PPT)的mRNA的产生在背根神经节(DRG)神经元中受神经生长因子(NGF)调节。为了探究NGF调节PPT mRNA产生的机制,我们用含有与报告基因氯霉素乙酰转移酶(CAT)相连的牛PPT启动子的质粒转染了PC12细胞和F11细胞。我们已鉴定出(i)在无NGF时表达所必需的PPT启动子内的功能元件,以及(ii)两个单独的区域,每个区域约250 bp,它们赋予对NGF的反应性。这两个区域都含有一个序列元件,类似于一个已知的转录因子结合位点,该位点存在于其他几个受NGF调节的基因中。