Mösch H U, Graf R, Schmidheini T, Braus G
Institute of Microbiology, Swiss Federal Institute of Technology, ETH, Zürich.
EMBO J. 1990 Sep;9(9):2951-7. doi: 10.1002/j.1460-2075.1990.tb07487.x.
The yeast TRP4 promoter contains three responsive elements (GCREs) for the 'general control' transcriptional activator GCN4, which are arranged in two upstream elements, UAS1 (GCRE1) and UAS2 (GCRE2 and GCRE3). A point mutation analysis of these elements revealed that all three GCREs are required for GCN4-dependent transcription, but none are involved in basal transcription. Basal transcription and GCN4-dependent transcription use completely different initiator elements in the TRP4 promoter. UAS1 acts synergistically with UAS2 to activate the GCN4-dependent transcription of TRP4. A consensus TATA box can functionally replace the UAS2 element to allow normal GCN4-dependent transcription, suggesting that UAS2 is analogous to the TATA element of other promoters. GCN4 might therefore activate transcription by exhibiting two alternative functions within the natural TRP4 promoter.
酵母TRP4启动子包含三个用于“一般调控”转录激活因子GCN4的响应元件(GCRE),它们排列在两个上游元件UAS1(GCRE1)和UAS2(GCRE2和GCRE3)中。对这些元件的点突变分析表明,所有三个GCRE都是GCN4依赖性转录所必需的,但没有一个参与基础转录。基础转录和GCN4依赖性转录在TRP4启动子中使用完全不同的起始元件。UAS1与UAS2协同作用以激活TRP4的GCN4依赖性转录。一个共有TATA框可以在功能上替代UAS2元件以允许正常的GCN4依赖性转录,这表明UAS2类似于其他启动子的TATA元件。因此,GCN4可能通过在天然TRP4启动子内展现两种替代功能来激活转录。