Hoopes B C, LeBlanc J F, Hawley D K
Institute of Molecular Biology and Department of Chemistry, University of Oregon, Eugene, OR 97403, USA.
J Mol Biol. 1998 Apr 17;277(5):1015-31. doi: 10.1006/jmbi.1998.1651.
We have examined the role of the TATA box in determining transcription initiation frequency in vitro by studying a collection of promoters containing different TATA sequences in the context of the adenovirus major late promoter. In addition to measuring transcription rates, we have determined how the sequence changes affected the association and dissociation kinetics and the affinity of TBP binding. We observed that transcription from promoters containing the highest affinity TATA boxes is limited by the rate with which TBP associates with the promoter. In contrast, transcription from promoters containing lower affinity TATA boxes appears to be limited both by how much TBP is bound and by the relatively low occupancy of the conformation that can undergo subsequent steps in preinitiation complex assembly. The implications of these results in understanding the mechanism of transcription enhancement by transcriptional activators is discussed.
我们通过研究腺病毒主要晚期启动子背景下一系列含有不同TATA序列的启动子,考察了TATA框在体外确定转录起始频率中的作用。除了测量转录速率,我们还确定了序列变化如何影响TBP结合的缔合和解离动力学以及亲和力。我们观察到,含有最高亲和力TATA框的启动子的转录受TBP与启动子缔合速率的限制。相比之下,含有较低亲和力TATA框的启动子的转录似乎既受TBP结合量的限制,也受能够经历起始前复合物组装后续步骤的构象相对低占有率的限制。讨论了这些结果在理解转录激活剂增强转录机制方面的意义。