Csordás-Tóth E, Boros I, Venetianer P
Nucleic Acids Res. 1979 Dec 20;7(8):2189-97. doi: 10.1093/nar/7.8.2189.
The nucleotide sequence of the promoter region for the rrnB gene of E. coli had been determined by the Maxam-Gilbert technique. The 700 bp long sequence had been compared with the published sequences of four other rRNA promoter regions. The rrnB sequence was found to be homologous with the rrnA promoter sequence till the 370th base upstream from the coding region of mature 16S rRNA. The significance of this homology is discussed and a tentative model is proposed to account for the unusual properties of the rRNA promoters.
大肠杆菌rrnB基因启动子区域的核苷酸序列已通过马克萨姆-吉尔伯特技术测定。已将这段700 bp长的序列与其他四个rRNA启动子区域已发表的序列进行了比较。发现rrnB序列与rrnA启动子序列在成熟16S rRNA编码区上游第370个碱基之前是同源的。讨论了这种同源性的意义,并提出了一个初步模型来解释rRNA启动子的异常特性。