Baylis H A, Bibb M J
John Innes Institute of Plant Science Research, Norwich, UK.
Mol Microbiol. 1988 Sep;2(5):569-79. doi: 10.1111/j.1365-2958.1988.tb00065.x.
The nucleotide sequence of 2.5 kb of the Streptomyces coelicolor A3(2) rRNA gene set rrnD, extending from upstream of the 16S rRNA gene to the putative 5' end of the 23S rRNA gene, has been determined (Baylis and Bibb, 1987; this paper). In addition to locating the 5' end of the 16S rRNA gene, nuclease S1 mapping identified seven RNA 5' end-points upstream of the 16S rRNA gene; four of these were coincident with transcriptional initiation points for S. coelicolor A3(2) RNA polymerase in vitro and were consequently regarded as in vivo transcription start points for promoters p1 to p4. One end-point identified by nuclease S1 mapping localized a putative processing site analogous to those found upstream of 16S rRNA genes in other eubacteria. Sequence motifs similar to those discovered in low G+C Gram-positive bacteria were found associated with two of the promoters and the processing site. A probable protein coding region was observed upstream of the promoter region.
天蓝色链霉菌A3(2)rRNA基因集rrnD的2.5kb核苷酸序列已被测定,该序列从16S rRNA基因的上游延伸至23S rRNA基因的假定5'端(Baylis和Bibb,1987年;本文)。除了确定16S rRNA基因的5'端外,核酸酶S1图谱还在16S rRNA基因上游鉴定出七个RNA 5'端点;其中四个与天蓝色链霉菌A3(2)RNA聚合酶体外转录起始点重合,因此被视为启动子p1至p4的体内转录起始点。核酸酶S1图谱鉴定出的一个端点定位了一个类似于在其他真细菌16S rRNA基因上游发现的假定加工位点。在两个启动子和加工位点发现了与在低G+C革兰氏阳性细菌中发现的序列基序相似的序列。在启动子区域上游观察到一个可能的蛋白质编码区域。