Carthew R W, Chodosh L A, Sharp P A
Cell. 1985 Dec;43(2 Pt 1):439-48. doi: 10.1016/0092-8674(85)90174-6.
A gel electrophoresis DNA binding assay has been used to identify proteins in HeLa cell extracts that specifically bind to the major late promoter of adenovirus. A major late promoter transcription factor MLTF has been detected as a discrete protein-DNA complex. MLTF binds specifically and with high affinity to sequences upstream of the TATA box of the major late promoter. This factor protects a 17 bp (-50 to -66) region in a DNAase I footprinting assay. The same region has been shown to be important for efficient transcription from the major late promoter both in vivo and in vitro. MLTF stimulates in vitro transcription only from a template containing this upstream region. The binding, footprinting, and transcription-stimulatory activities of MLTF cofractionate through two chromatographic steps. These results suggest that direct binding of MLTF to an upstream element activates transcription from the major late promoter.
凝胶电泳DNA结合试验已用于鉴定HeLa细胞提取物中能特异性结合腺病毒主要晚期启动子的蛋白质。一种主要晚期启动子转录因子MLTF已被检测为一种离散的蛋白质-DNA复合物。MLTF能特异性且高亲和力地结合主要晚期启动子TATA框上游的序列。在DNA酶I足迹试验中,该因子可保护一个17bp(-50至-66)的区域。同一区域已被证明在体内和体外对主要晚期启动子的高效转录都很重要。MLTF仅从含有该上游区域的模板刺激体外转录。MLTF的结合、足迹和转录刺激活性通过两个色谱步骤共分级分离。这些结果表明,MLTF与上游元件的直接结合激活了主要晚期启动子的转录。