Gerrard Lesley, Howard Mark, Paterson Trevor, Thippeswamy Thimmasettappa, Quinn John P, Haddley Kate
Roslin Institute, Roslin, Midlothian EH25 9PS, UK.
Neuropeptides. 2005 Oct;39(5):475-83. doi: 10.1016/j.npep.2005.08.004. Epub 2005 Sep 29.
The rat preprotachykinin A (rtPPTA) promoter fragment spanning -865+92, relative to the major transcriptional start, has previously been demonstrated to be nerve growth factor (NGF) responsive in primary cultures of rat dorsal root ganglion (DRG) neurones [Harrison, P.T., Dalziel, R.G., Ditchfield, N.A., Quinn, J.P., 1999. Neuronal-specific and nerve growth factor-inducible expression directed by the preprotachykinin-A promoter delivered by an adeno-associated virus vector. Neuroscience 94, 997-1003]. In this communication, we demonstrate that an E box element at -60, in part, regulates the activity of this rtPPT-A promoter fragment in DRG neurones in response to NGF. Differential regulation of the promoter is observed in the presence or absence of NGF when the E Box site is present. Under basal conditions binding of proteins to this -60 element may antagonise promoter activity. Hence, in the absence of NGF, mutation of the -60 E box increased reporter gene expression. Further, comparison of levels of reporter gene expression supported by both WT and mutated promoter indicate that in the presence of NGF the -60 E box element also plays a role as an activator domain. This represents a novel mechanism for NGF regulation of rtPPT-A. Similarly, an important role for this signalling pathway was observed in neonate rat DRG neuronal cultures, which require NGF for their survival, namely mutation of the -60 element resulted in higher levels of reporter gene expression.
相对于主要转录起始位点,跨越-865至+92的大鼠前速激肽原A(rtPPTA)启动子片段,先前已被证明在大鼠背根神经节(DRG)神经元的原代培养物中对神经生长因子(NGF)有反应[哈里森,P.T.,达尔齐尔,R.G.,迪奇菲尔德,N.A.,奎因,J.P.,1999年。腺相关病毒载体传递的前速激肽原A启动子指导的神经元特异性和神经生长因子诱导性表达。神经科学94,997 - 1003]。在本通讯中,我们证明位于-60的一个E盒元件部分调节该rtPPT - A启动子片段在DRG神经元中对NGF的反应活性。当E盒位点存在时,在有或没有NGF的情况下观察到启动子的差异调节。在基础条件下,蛋白质与这个-60元件的结合可能拮抗启动子活性。因此,在没有NGF的情况下,-60 E盒的突变增加了报告基因的表达。此外,野生型和突变型启动子支持的报告基因表达水平的比较表明,在有NGF的情况下,-60 E盒元件也作为激活域发挥作用。这代表了NGF调节rtPPT - A的一种新机制。同样,在新生大鼠DRG神经元培养物中观察到该信号通路的重要作用,这些神经元的存活需要NGF,即-60元件的突变导致报告基因表达水平更高。