Nakamura Y, Mizusawa S
EMBO J. 1985 Feb;4(2):527-32. doi: 10.1002/j.1460-2075.1985.tb03660.x.
Previous work has shown that the Escherichia coli nusA gene codes for a protein which regulates transcription termination. The 16.0-kb EcoRI DNA fragment that includes the nusA gene, codes for at least eight bacterial proteins of mol. wts. 48 000 (argG), 21 000 (p21), 64 000 (nusA), 120 000 (IF2 alpha)-(infB), 91 000 (IF2 beta)(infB), 15 000 (p15), 10 000 (rpsO) and 85 000 (pnp). We have constructed several deletion and fusion derivatives from this cloned DNA and examined in vivo the structure and expression of these genes. First, the promoter functional in vivo for the nusA gene was mapped at approximately 800 bp upstream of the nusA structural gene. Second, the synthesis of five proteins, p21, NusA, IF2 alpha, IF2 beta (and p15) proteins, was affected by the deletion of the nusA promoter. Third, these same five proteins were hyperproduced after fusion of the DNA fragment to the lambda pL promoter. In addition, subcloning experiments revealed that the p15 gene is expressed by the read-through transcription from the infB gene. These results lead us to conclude that the genes coding for the p21, NusA, InfB (IF2 alpha and IF2 beta), and p15 proteins form a single-transcriptional unit ('nusA-infB operon') in vivo and that rpsO and pnp genes do not belong to the same operon. The in vivo attenuation site of this operon is described.
先前的研究表明,大肠杆菌nusA基因编码一种调节转录终止的蛋白质。包含nusA基因的16.0 kb EcoRI DNA片段至少编码8种分子量的细菌蛋白。分别为48 000(argG)、21 000(p21)、64 000(nusA)、120 000(IF2α)-(infB)、91 000(IF2β)(infB)、15 000(p15)、10 000(rpsO)和85 000(pnp)。我们从这个克隆的DNA构建了几个缺失和融合衍生物,并在体内研究了这些基因的结构和表达。首先,在体内对nusA基因起作用的启动子定位在nusA结构基因上游约800 bp处。其次,p21、NusA、IF2α、IF2β(和p15)这五种蛋白质的合成受到nusA启动子缺失的影响。第三,将DNA片段与λ pL启动子融合后,这相同的五种蛋白质过量产生。此外,亚克隆实验表明,p15基因是通过从infB基因的通读转录来表达的。这些结果使我们得出结论,编码p21、NusA、InfB(IF2α和IF2β)和p15蛋白的基因在体内形成一个单一转录单元(“nusA-infB操纵子”),而rpsO和pnp基因不属于同一个操纵子。本文描述了该操纵子在体内的衰减位点。