Kleinert H, Bredow S, Benecke B J
Department of Biochemistry, Faculty of Chemistry, Ruhr-University, Bochum, FRG.
EMBO J. 1990 Mar;9(3):711-8. doi: 10.1002/j.1460-2075.1990.tb08164.x.
The 5'-flanking sequences required for expression of a human 7S K RNA gene have been defined by mutant analysis. A -111 upstream deletion mutant showed full activity when analysed by in vitro transcription with HeLa cell extracts. In contrast, upon transfection into intact cells, this mutant only revealed a basal level activity of approximately 6% as compared to the wild-type promoter up to position -252. The deleted upstream sequence element acts as a transcriptional activator in vivo, in a strictly position and orientation-dependent manner. Two octamer-like binding motifs observed within this upstream sequence were both dispensable for proper function of this RNA polymerase III promoter in vivo. Instead, a detailed analysis of this region identified a CACCC-box element, together with its surrounding base pairs, as the essential upstream element required for expression of this 7S K RNA gene in vivo. Furthermore, this CACCC-box is centered within a footprint obtained with HeLa cell nuclear proteins.
通过突变分析确定了人7S K RNA基因表达所需的5'侧翼序列。用HeLa细胞提取物进行体外转录分析时,-111上游缺失突变体显示出完全活性。相反,转染到完整细胞后,与野生型启动子(至-252位)相比,该突变体仅显示约6%的基础水平活性。缺失的上游序列元件在体内以严格的位置和方向依赖性方式作为转录激活因子起作用。在该上游序列中观察到的两个八聚体样结合基序对于该RNA聚合酶III启动子在体内的正常功能均非必需。相反,对该区域的详细分析确定了一个CACCC框元件及其周围的碱基对,作为该7S K RNA基因在体内表达所需的必需上游元件。此外,该CACCC框位于用HeLa细胞核蛋白获得的足迹中心。