Little S, Hyde S, Campbell C J, Lilley R J, Robinson M K
Department of Microbial Systems, Celltech Gp Ltd., Berkshire, United Kingdom.
J Bacteriol. 1989 Jun;171(6):3518-22. doi: 10.1128/jb.171.6.3518-3522.1989.
In an attempt to express the two distal genes of the Escherichia coli threonine operon, the majority of the first gene in the operon, thrA, was removed and a series of transcriptional fusions were constructed placing the thrB and thrC genes downstream of either the trp or hybrid tac promoter. Analysis of the proteins produced by cells containing these fusions revealed that although the distal gene, thrC, was efficiently expressed, the proximal gene, thrB, was not expressed at a detectable level. A translational fusion was constructed which fused the cat gene in phase to the last 800 base pairs of thrA followed by thrB and thrC. Cells containing this fusion produced high levels of both the thrB and thrC gene products, showing that translation of thrB requires translation through thrA; thus, thrA and thrB are translationally coupled. In addition, it was found that a sequence between 220 and 57 base pairs before the start of thrB was necessary to allow translational coupling to occur.
为了表达大肠杆菌苏氨酸操纵子的两个远端基因,操纵子中第一个基因thrA的大部分被去除,并构建了一系列转录融合体,将thrB和thrC基因置于trp或杂合tac启动子的下游。对含有这些融合体的细胞产生的蛋白质进行分析发现,尽管远端基因thrC高效表达,但近端基因thrB未在可检测水平表达。构建了一个翻译融合体,将cat基因与thrA的最后800个碱基对同相位融合,随后是thrB和thrC。含有这种融合体的细胞产生了高水平的thrB和thrC基因产物,表明thrB的翻译需要通过thrA进行;因此,thrA和thrB是翻译偶联的。此外,还发现thrB起始前220至57个碱基对之间的序列是允许翻译偶联发生所必需的。