Goldfarb A
Nucleic Acids Res. 1981 Feb 11;9(3):519-27. doi: 10.1093/nar/9.3.519.
Analysis of primary transcripts made by Escherichia coli RNA polymerase on T4 DNA containing an intact or partially deleted tRNA gene cluster demonstrates that the T4 tRNA genes are transcribed from two promoters differing in their strength. The stronger (P1) and the weaker (P2) promoters are located at distances of 1 kb and 1.5 kb from the tRNA genes, respectively. Selective initiation of individual transcripts with dinucleotides shows that P1 and P2 promoters contain the sequences TAT and CAC respectively. The two-promoter organisation of the tRNA cluster may reflect two superimposed mechanisms of gene expression in T4-infected bacteria.
对大肠杆菌RNA聚合酶在含有完整或部分缺失tRNA基因簇的T4 DNA上产生的初级转录本进行分析表明,T4 tRNA基因由两个强度不同的启动子转录。较强的启动子(P1)和较弱的启动子(P2)分别位于距tRNA基因1 kb和1.5 kb处。用二核苷酸对单个转录本进行选择性起始表明,P1和P2启动子分别含有序列TAT和CAC。tRNA簇的双启动子结构可能反映了T4感染细菌中基因表达的两种叠加机制。