Elder G A, Liang Z, Snyder S E, Lazzarini R A
Brookdale Center for Molecular Biology, Mount Sinai School of Medicine, New York, NY 10029.
Brain Res Mol Brain Res. 1992 Sep;15(1-2):99-107. doi: 10.1016/0169-328x(92)90156-6.
In order to identify potential regulatory elements of the human mid-sized (M) neurofilament (NF) gene we preformed DNase I footprinting, gel mobility shift assays and methylation interference studies with probes from the NF(M) immediate 5' flanking region. These studies identified multiple sites for DNA-binding proteins including four Sp1 sites, and single sites each for members of the NF-1 and AP-1 families of DNA binding proteins. In addition a binding site within a pyrimidine tract likely binds a novel DNA-binding protein which also interacts with the human NF(H) gene promoter. Factors that bind to these sites are found in both neural and non-neural cells suggesting that the NF(M) promoter may not contain tissue specific regulatory signals. In transient assays, addition of these binding sites to an NF(M) minimal promoter containing only a TATA box lead to a greater than 40-fold activation of transcription over background. Progressive 5' deletions reduced expression in a step wise manner suggesting that all the factors likely act synergistically as positive regulators of transcription.
为了鉴定人类中型(M)神经丝(NF)基因的潜在调控元件,我们使用来自NF(M)紧邻5'侧翼区域的探针进行了DNA酶I足迹分析、凝胶迁移率变动分析和甲基化干扰研究。这些研究确定了多个DNA结合蛋白位点,包括四个Sp1位点,以及DNA结合蛋白NF-1家族和AP-1家族成员各自的单个位点。此外,嘧啶序列中的一个结合位点可能结合一种新型DNA结合蛋白,该蛋白也与人类NF(H)基因启动子相互作用。在神经细胞和非神经细胞中均发现了与这些位点结合的因子,这表明NF(M)启动子可能不包含组织特异性调控信号。在瞬时分析中,将这些结合位点添加到仅包含TATA框的NF(M)最小启动子中,导致转录活性比背景高40倍以上。5'端逐步缺失以逐步方式降低表达,这表明所有这些因子可能作为转录的正调控因子协同发挥作用。