Tuggle C K, Fuchs J A
EMBO J. 1986 May;5(5):1077-85. doi: 10.1002/j.1460-2075.1986.tb04325.x.
The ribonucleotide reductase genes (nrd) are induced by thymine starvation. Deletion analysis of the sequences upstream of the cloned nrd genes was used to identify several regulatory regions. The start of transcription (nrdP) was mapped 110 bp upstream of nrdA, the first structural gene. A site required for positive regulation of nrd was mapped 135 bp upstream of nrdP in a region with two direct repeat sequences as well as potential secondary structure. Two other sites (one upstream of nrdP, the other downstream) were identified as sequences whose deletion markedly increase expression. These latter sites show sequence homology and probably interact since the effects of their individual deletion are not additive when combined.
核糖核苷酸还原酶基因(nrd)在胸腺嘧啶饥饿时被诱导。通过对克隆的nrd基因上游序列进行缺失分析来鉴定几个调控区域。转录起始点(nrdP)被定位在第一个结构基因nrdA上游110 bp处。nrd正向调控所需的一个位点被定位在nrdP上游135 bp处的一个区域,该区域有两个直接重复序列以及潜在的二级结构。另外两个位点(一个在nrdP上游,另一个在下游)被鉴定为缺失后会显著增加表达的序列。后两个位点显示出序列同源性,并且可能相互作用,因为当它们单独缺失的效应组合在一起时不是累加的。