Symes A, Gearan T, Fink J S
Massachusetts General Hospital, Department of Neurology, Harvard Medical School, Boston, USA.
J Neurosci Res. 1998 Apr 1;52(1):93-104. doi: 10.1002/(SICI)1097-4547(19980401)52:1<93::AID-JNR9>3.0.CO;2-F.
The vasoactive intestinal peptide cytokine response element (VIP CyRE) is responsible for mediating the transcriptional induction of the VIP gene to the neuropoietic cytokines leukemia inhibitory factor (LIF) and ciliary neurotrophic factor (CNTF). In investigating the sequence and function of the CyRE, we found a region of DNA with homology to the distal NFAT site in the IL-2 promoter. In this paper we characterize this sequence and show that the VIP NFAT site recognizes T cell NFAT with similar affinity to the previously characterized IL-2 NFAT site. However, despite its location in the middle of the CyRE, we find no CNTF/LIF induced binding to it. Instead we show that in NBFL neuroblastoma cells, the calcium ionophore A23187 induces a protein to bind to the VIP NFAT site. This A23187-mediated induction of nuclear protein binding to an NFAT oligonucleotide is dependent on extracellular calcium but not dependent on de novo protein synthesis. Thus, this protein has the characteristics of an NFAT-like protein and is recognized by an NFAT3-specific antiserum suggesting that it is indeed an NFAT protein. The location of the NFAT site in the VIP CyRE suggests that this may be one mechanism through which different signaling pathways engage in cross talk to alter VIP gene transcription.
血管活性肠肽细胞因子反应元件(VIP CyRE)负责介导VIP基因对神经生成细胞因子白血病抑制因子(LIF)和睫状神经营养因子(CNTF)的转录诱导。在研究CyRE的序列和功能时,我们发现了一段与IL-2启动子中远端NFAT位点具有同源性的DNA区域。在本文中,我们对该序列进行了表征,并表明VIP NFAT位点识别T细胞NFAT的亲和力与先前表征的IL-2 NFAT位点相似。然而,尽管它位于CyRE的中间,我们发现CNTF/LIF并未诱导蛋白与之结合。相反,我们发现在NBFL神经母细胞瘤细胞中,钙离子载体A23187可诱导一种蛋白与VIP NFAT位点结合。这种由A23187介导的核蛋白与NFAT寡核苷酸的结合诱导依赖于细胞外钙,但不依赖于从头合成蛋白。因此,这种蛋白具有类NFAT蛋白的特征,并被NFAT3特异性抗血清识别,表明它确实是一种NFAT蛋白。VIP CyRE中NFAT位点的位置表明,这可能是不同信号通路进行串扰以改变VIP基因转录的一种机制。