de Boer H A, Gilbert S F, Nomura M
Cell. 1979 May;17(1):201-9. doi: 10.1016/0092-8674(79)90308-8.
The nucleotide sequences have been determined for the promoter regions of two ribosomal RNA operons, rrnA and rrnE, in E. coli. The sequences cover the two in vitro transcription start sites identified for each operon (Gilbert, der Boer and Nomura, 1979). The first two start sites are 283 and 291 bp preceding the mature 16S rRNA (m16S rNA) coding regions for rrnE and rrnA, respectively; the second start sites are 174 and 174 +/- 1 bp preceding the m16S rRNA coding regions for rrnE and rrnA, respectively. Each of these start sites has an identifiable "Pribnow box" sequence 6-7 bp upstream from the start site. The nucleotide sequences of the two operons have nearly complete homology from the m16S rRNA coding regions to positions 145 bp upstream from those regions, and at the regions surrounding the Pribnow boxes preceding the first start sites. The DNA sequences indicate that the RNAs transcribed from the first start sites of rrnE and rrnA are quite different in their first 150 nucleotides. These heterogeneous regions, however, precede the RNAse III cleavage sites (deduced previously by Young and Steitz, 1978), and the "precursor 16S rRNA" molecules are largely homogeneous. The nucleotide sequences of the promoter regions of the two rRNA operons are also compared with those or rrnD and rrnX, determined by Young and Steitz (1979), and some common features are discussed.
已经测定了大肠杆菌中两个核糖体RNA操纵子rrnA和rrnE启动子区域的核苷酸序列。这些序列涵盖了为每个操纵子确定的两个体外转录起始位点(吉尔伯特、德布尔和野村,1979年)。rrnE和rrnA的前两个起始位点分别在成熟16S rRNA(m16S rNA)编码区域之前283和291 bp处;rrnE和rrnA的第二个起始位点分别在m16S rRNA编码区域之前174和174 +/- 1 bp处。这些起始位点中的每一个在起始位点上游6 - 7 bp处都有一个可识别的“Pribnow框”序列。从m16S rRNA编码区域到这些区域上游145 bp处,以及在第一个起始位点之前的Pribnow框周围区域,这两个操纵子的核苷酸序列几乎完全同源。DNA序列表明,从rrnE和rrnA的第一个起始位点转录的RNA在前150个核苷酸中差异很大。然而,这些异质区域在RNA酶III切割位点之前(先前由扬和施泰茨推导得出,1978年),并且“前体16S rRNA”分子在很大程度上是同质的。还将这两个rRNA操纵子启动子区域的核苷酸序列与扬和施泰茨(1979年)测定的rrnD和rrnX的序列进行了比较,并讨论了一些共同特征。