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一个近端E盒调节神经生长因子对培养的背根神经节神经元中大鼠PPT-A启动子活性的影响。

A proximal E-box modulates NGF effects on rat PPT-A promoter activity in cultured dorsal root ganglia neurones.

作者信息

Gerrard Lesley, Howard Mark, Paterson Trevor, Thippeswamy Thimmasettappa, Quinn John P, Haddley Kate

机构信息

Roslin Institute, Roslin, Midlothian EH25 9PS, UK.

出版信息

Neuropeptides. 2005 Oct;39(5):475-83. doi: 10.1016/j.npep.2005.08.004. Epub 2005 Sep 29.

Abstract

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.

摘要

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。

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