Iyer V, Struhl K
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Mol Cell Biol. 1995 Dec;15(12):7059-66. doi: 10.1128/MCB.15.12.7059.
The yeast his3 promoter region contains two TATA elements, TC and TR, that are differentially utilized in constitutive his3 transcription and Gcn4-activated his3 transcription. TR contains the canonical TATAAA sequence, whereas TC is an extended region that lacks a conventional TATA sequence and does not support transcription in vitro. Surprisingly, differential his3 TATA-element utilization does not depend on specific properties of activator proteins but, rather, is determined by the overall level of his3 transcription. At low levels of transcription, the upstream TC is preferentially utilized, even though it is inherently a much weaker TATA element than TR. The TATA elements are utilized equally at intermediate levels, whereas TR is strongly preferred at high levels of transcription. This characteristic behavior can be recreated by replacing TC with moderately functional derivatives of a conventional TATA element, suggesting that TC is a collection of weak TATA elements. Analysis of promoters containing two biochemically defined TATA elements indicates that differential utilization occurs when the upstream TATA element is weaker than the downstream element. In other situations, the upstream TATA element is preferentially utilized in a manner that is independent of the overall level of transcription. Thus, in promoters containing multiple TATA elements, relative utilization not only depends on the quality and arrangement of the TATA elements but can vary with the overall level of transcriptional stimulation. We suggest that differential TATA utilization results from the combination of an intrinsic preference for the upstream element and functional saturation of weak TATA elements at low levels of transcriptional stimulation.
酵母his3启动子区域包含两个TATA元件,即TC和TR,它们在组成型his3转录和Gcn4激活的his3转录中被差异利用。TR包含典型的TATAAA序列,而TC是一个扩展区域,缺乏传统的TATA序列,并且在体外不支持转录。令人惊讶的是,his3 TATA元件的差异利用并不取决于激活蛋白的特定特性,而是由his3转录的总体水平决定。在低转录水平时,上游的TC优先被利用,尽管它本质上是一个比TR弱得多的TATA元件。在中等转录水平时,两个TATA元件被同等利用,而在高转录水平时,TR被强烈优先选择。通过用传统TATA元件的适度功能性衍生物取代TC,可以重现这种特征行为,这表明TC是一组弱TATA元件。对含有两个生化定义的TATA元件的启动子的分析表明,当上游TATA元件比下游元件弱时,会发生差异利用。在其他情况下,上游TATA元件以与转录总体水平无关的方式被优先利用。因此,在含有多个TATA元件的启动子中,相对利用不仅取决于TATA元件的质量和排列,还会随转录刺激的总体水平而变化。我们认为,TATA的差异利用是由对上游元件的内在偏好和在低水平转录刺激下弱TATA元件的功能饱和共同作用的结果。