Deans Z, Dawson S J, Xie J, Young A P, Wallace D, Latchman D S
Department of Molecular Pathology, University College London Medical School, London W1P 6DB, United Kingdom.
J Biol Chem. 1996 Dec 13;271(50):32153-8. doi: 10.1074/jbc.271.50.32153.
The Oct-2 transcription factor has been shown previously to repress both the cellular tyrosine hydroxylase and the herpes simplex virus immediate-early genes in neuronal cells. Here we identify the gene encoding the neuronal nitric-oxide synthase (nNOS) as the first example of a gene activated in neuronal cells by Oct-2. The levels of the nNOS mRNA and protein are greatly reduced in neuronal cell lines in which Oct-2 levels have been reduced by an antisense method, although these cells have enhanced levels of tyrosine hydroxylase. Moreover, the nNOS gene regulatory region is activated by Oct-2 expression vectors upon cotransfection into both neuronal and non-neuronal cells, and this response is dependent upon a 20-amino acid region within the COOH-terminal activation domain of Oct-2. Of the two closely linked promoters that drive nNOS gene expression, only the downstream 5.1 promoter is activated by Oct-2, whereas the 5.2 promoter is unaffected. These effects are discussed in terms of the potential role of Oct-2 in regulating nNOS expression in the nervous system.
先前已表明,Oct-2转录因子在神经元细胞中可抑制细胞酪氨酸羟化酶和单纯疱疹病毒立即早期基因。在此,我们确定编码神经元型一氧化氮合酶(nNOS)的基因是Oct-2在神经元细胞中激活的首个基因实例。在通过反义方法降低Oct-2水平的神经元细胞系中,nNOS mRNA和蛋白质水平大幅降低,尽管这些细胞中酪氨酸羟化酶水平有所升高。此外,将Oct-2表达载体共转染到神经元和非神经元细胞中时,nNOS基因调控区域会被激活,且这种反应依赖于Oct-2羧基末端激活域内的一个20个氨基酸的区域。在驱动nNOS基因表达的两个紧密相连的启动子中,只有下游的5.1启动子被Oct-2激活,而5.2启动子不受影响。本文从Oct-2在调节神经系统中nNOS表达的潜在作用方面对这些效应进行了讨论。