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A Random Screen Using a Novel Reporter Assay System Reveals a Set of Sequences That Are Preferred as the TATA or TATA-Like Elements in the CYC1 Promoter of Saccharomyces cerevisiae

机译:使用新型记者分析系统的随机屏幕显示了一组优选为酿酒酵母CYC1启动子中的TATA或TATA样元件的序列。

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摘要

In Saccharomyces cerevisiae, the core promoters of class II genes contain either TATA or TATA-like elements to direct accurate transcriptional initiation. Genome-wide analyses show that the consensus sequence of the TATA element is TATAWAWR (8 bp), whereas TATA-like elements carry one or two mismatches to this consensus. The fact that several functionally distinct TATA sequences have been identified indicates that these elements may function, at least to some extent, in a gene-specific manner. The purpose of the present study was to identify functional TATA sequences enriched in one particular core promoter and compare them with the TATA or TATA-like elements that serve as the pre-initiation complex (PIC) assembly sites on the yeast genome. For this purpose, we conducted a randomized screen of the TATA element in the CYC1 promoter by using a novel reporter assay system and identified several hundreds of unique sequences that were tentatively classified into nine groups. The results indicated that the 7 bp TATA element (i.e., TATAWAD) and several sets of TATA-like sequences are preferred specifically by this promoter. Furthermore, we find that the most frequently isolated TATA-like sequence, i.e., TATTTAAA, is actually utilized as a functional core promoter element for the endogenous genes, e.g., ADE5,7 and ADE6. Collectively, these results indicate that the sequence requirements for the functional TATA or TATA-like elements in one particular core promoter are not as stringent. However, the variation of these sequences differs significantly from that of the PIC assembly sites on the genome, presumably depending on promoter structures and reflecting the gene-specific function of these sequences.
机译:在酿酒酵母中,II类基因的核心启动子包含TATA或TATA样元件来指导准确的转录起始。全基因组分析表明,TATA元件的共有序列为TATAWAWR(8 bp),而TATA样元件带有一个或两个错配。已经鉴定出几个功能上不同的TATA序列的事实表明,这些元件可以至少在某种程度上以基因特异性的方式起作用。本研究的目的是鉴定富含一种特定核心启动子的功能性TATA序列,并将其与充当酵母基因组上的预起始复合物(PIC)装配位点的TATA或TATA样元件进行比较。为此,我们使用新型报告基因检测系统对CYC1启动子中的TATA元件进行了随机筛选,并鉴定了数百个独特的序列,这些序列暂定分为9组。结果表明,该启动子特别优选7bp的TATA元件(即TATAWAD)和几组TATA样序列。此外,我们发现最常分离的TATA样序列,即TATTTAAA,实际上被用作内源基因例如ADE5,7和ADE6的功能性核心启动子元件。总的来说,这些结果表明在一个特定的核心启动子中功能性TATA或TATA样元件的序列要求并不那么严格。但是,这些序列的变异与基因组上PIC装配位点的变异显着不同,大概取决于启动子的结构并反映了这些序列的基因特异性功能。

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