Healy A M, Zitomer R S
Department of Biological Sciences State University of New York, Albany 12222.
Curr Genet. 1990 Aug;18(2):105-9. doi: 10.1007/BF00312597.
While RNA polymerase II of the yeast Saccharomyces cerevisiae initiates transcription at discrete sites, these sites are located over a wide range of distances from the TATA box for different genes. This variability has led to a number of proposals for consensus sequences located at the initiation site which, in conjunction with the TATA box, would direct initiation. We tested this hypothesis via oligonucleotide-directed mutagenesis, by placing the sequence CAAG, a member of one of these consensus sequences, upstream of the coding sequence of the CYC7 gene at a site at which initiation does not occur. The distance between the TATA sequence and this putative initiation site was varied by inserting it into the wild-type gene and three deletion mutants. The results demonstrated that this sequence can serve as an initiation site when located 49, 77, or 106 bp from the TATA sequence, but not when located 30 bp away.
虽然酿酒酵母的RNA聚合酶II在离散位点起始转录,但对于不同基因而言,这些位点与TATA框的距离范围很广。这种变异性引发了许多关于位于起始位点的共有序列的提议,这些共有序列与TATA框一起指导起始。我们通过寡核苷酸定向诱变来检验这一假设,将这些共有序列之一的成员序列CAAG置于CYC7基因编码序列上游一个不发生起始的位点。通过将其插入野生型基因和三个缺失突变体中,改变TATA序列与这个假定起始位点之间的距离。结果表明,当该序列距离TATA序列49、77或106 bp时可作为起始位点,但距离30 bp时则不行。