Rotheneder H, Grabner M, Wintersberger E
Institut für Molekularbiologie, Universität Wien, Austria.
Nucleic Acids Res. 1991 Dec 25;19(24):6805-9. doi: 10.1093/nar/19.24.6805.
The intron 2 of the murine thymidine kinase (TK) gene was observed to contain two DNase hypersensitive site. In vitro footprinting experiments indicated specific binding sites for nuclear proteins which were characterized within the sequence of intron 2. Two GC boxes (binding sites for transcription factor SP1) and two new protein binding regions, one at the promoter proximal end of intron 2, the other one close to the border to exon 3 were found. Oligonucleotides were synthesized comprising the two new binding sites and were shown in gel mobility shift experiments to be capable of forming specific complexes with nuclear proteins. These proteins are present in growing as well as in quiescent cells suggesting that the sites described here do not contribute to growth regulation of TK expression. That they might play a role in upregulation of TK expression is, however, indicated by the results of CAT assays in which inclusion of downstream sequences of the TK gene containing parts or all of intron 2 were found to positively modulate the activity of the TK promoter.
小鼠胸苷激酶(TK)基因的内含子2被观察到含有两个对脱氧核糖核酸酶敏感的位点。体外足迹实验表明,在核蛋白的特定结合位点在2号内含子序列中得以确定。发现了两个GC框(转录因子SP1的结合位点)和两个新的蛋白质结合区域,一个位于2号内含子的启动子近端,另一个靠近与外显子3的边界。合成了包含这两个新结合位点的寡核苷酸,并在凝胶迁移率变动实验中表明它们能够与核蛋白形成特定复合物。这些蛋白质在生长细胞和静止细胞中均存在,这表明此处描述的位点对TK表达的生长调节没有作用。然而,TK基因下游序列包含部分或全部2号内含子,在CAT分析结果中发现其可正向调节TK启动子的活性,这表明它们可能在TK表达上调中发挥作用。