Klein C, Struhl K
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Science. 1994 Oct 14;266(5183):280-2. doi: 10.1126/science.7939664.
The rate at which the TATA-binding protein (TBP) interacts with the TATA element and promotes transcription by RNA polymerase II was determined in yeast cells. A TBP derivative with altered TATA-element specificity was rapidly induced, and transcription from promoters with appropriately mutated TATA elements was measured. Without a functional activator protein, basal transcription was observed only after a lag of several hours. In contrast, GCN4-activated transcription occurred rapidly upon induction of the TBP derivative. These results suggest that accessibility of TBP to the chromatin template in vivo is rate limiting and that activation domains increase recruitment of TBP to the promoter.
在酵母细胞中测定了TATA结合蛋白(TBP)与TATA元件相互作用并促进RNA聚合酶II转录的速率。快速诱导出具有改变的TATA元件特异性的TBP衍生物,并测量来自具有适当突变的TATA元件的启动子的转录。在没有功能性激活蛋白的情况下,仅在数小时的延迟后才观察到基础转录。相比之下,在诱导TBP衍生物后,GCN4激活的转录迅速发生。这些结果表明,TBP在体内对染色质模板的可及性是限速的,并且激活域增加了TBP向启动子的募集。