Suppr超能文献

大鼠前速激肽原-A近端启动子中功能性E盒基序的表征

Characterisation of a functional E box motif in the proximal rat preprotachykinin-A promoter.

作者信息

Paterson J M, Morrison C F, Dobson S P, McAllister J, Quinn J P

机构信息

MRC Brain Metabolism Unit, Royal Edinburgh Hospital, UK.

出版信息

Neurosci Lett. 1995 May 26;191(3):185-8. doi: 10.1016/0304-3940(95)11588-n.

Abstract

Three E box motifs, which are upstream of the major transcriptional start site, have previously been characterised in the rat preprotachykinin-A (rPPT) promoter. Only one of these, in the proximal promoter spanning nucleotides -67 to -47, has been demonstrated to support reporter gene expression in clonal cell lines under basal growth conditions. Here we demonstrate that the reporter gene expression can be further induced by the action of phorbol 12-myristate 13-acetate (TPA) and nerve growth factor (NGF), respectively, in both HeLa and the neuronally derived PC12 cells. This response is due to the E box motif and not an overlapping consensus sequence for a putative AP1 element, a class of element previously demonstrated to respond to both TPA and NGF in these cell lines. Finally, we demonstrate that this E box motif can support similar levels of reporter gene expression in primary cultures of dorsal root ganglion neurons as observed in clonal cell lines, demonstrating that E box binding complexes can (1) function as a transcriptional regulator in dorsal root ganglion neurons and (2) bind to and therefore presumably regulate rPPT promoter activity.

摘要

在大鼠前速激肽原 -A(rPPT)启动子中,主要转录起始位点上游的三个E盒基序先前已被鉴定。在跨越核苷酸 -67至 -47的近端启动子中,其中只有一个已被证明在基础生长条件下能支持克隆细胞系中的报告基因表达。在此,我们证明在HeLa细胞和神经源性PC12细胞中,佛波醇12 -肉豆蔻酸酯13 -乙酸酯(TPA)和神经生长因子(NGF)的作用分别可进一步诱导报告基因表达。这种反应归因于E盒基序,而非假定的AP1元件的重叠共有序列,AP1元件是一类先前已证明在这些细胞系中对TPA和NGF均有反应的元件。最后,我们证明该E盒基序在背根神经节神经元的原代培养物中能支持与克隆细胞系中观察到的相似水平的报告基因表达,这表明E盒结合复合物能够(1)作为背根神经节神经元中的转录调节因子发挥作用,并且(2)结合并因此可能调节rPPT启动子活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验