Bell-Pedersen D, Galloway Salvo J L, Belfort M
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany.
J Bacteriol. 1991 Feb;173(3):1193-200. doi: 10.1128/jb.173.3.1193-1200.1991.
A transcription terminator has been identified within the coding sequence of the Escherichia coli thyA gene. Fusion of a relevant segment of the thyA structural gene to galK sequences showed that the terminator functions in vivo. Primer extension and Northern hybridization (RNA blot) analysis of thyA RNA suggested that the terminator acts as the transcription stop signal for an upstream gene and for thyA-specific transcripts. Results from antitermination studies utilizing a lambda PL-thyA fusion also offer evidence that the terminator is capable of attenuating thyA expression by reducing the amount of full-length thyA transcripts. This gene arrangement suggested that previous unsuccessful attempts to create a chromosomal thyA deletion in E. coli were attributable to the presence of the overlapping transcript. Introducing a deletion into the nonoverlapping portion of the cloned thyA gene and inserting a gene encoding kanamycin resistance produced a (delta thyA::Kmr) that was easily transferred to the chromosome of a recD host by marker replacement. This delta thyA::Kmr allele provides a useful and readily transducible chromosomal marker.
在大肠杆菌thyA基因的编码序列中已鉴定出一个转录终止子。将thyA结构基因的相关片段与galK序列融合表明,该终止子在体内发挥作用。对thyA RNA进行引物延伸和Northern杂交(RNA印迹)分析表明,该终止子作为上游基因和thyA特异性转录本的转录终止信号。利用λPL-thyA融合进行的抗终止研究结果也提供了证据,表明该终止子能够通过减少全长thyA转录本的量来减弱thyA的表达。这种基因排列表明,之前在大肠杆菌中创建染色体thyA缺失的尝试未成功是由于存在重叠转录本。在克隆的thyA基因的非重叠部分引入缺失并插入编码卡那霉素抗性的基因,产生了一个(ΔthyA::Kmr),它可以通过标记替换轻松转移到recD宿主的染色体上。这个ΔthyA::Kmr等位基因提供了一个有用且易于转导的染色体标记。