Wozniak D J
Department of Microbiology and Immunology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27157-1064.
J Bacteriol. 1994 Aug;176(16):5068-76. doi: 10.1128/jb.176.16.5068-5076.1994.
Pseudomonas aeruginosa is an extremely important opportunistic pathogen in immunocompromised individuals. Strains of P. aeruginosa isolated from chronic lung infections in patients with the genetic disease cystic fibrosis have a mucoid colony morphology. This phenotype is due to overproduction of the exopolysaccharide alginate, which is believed to confer a selective advantage on P. aeruginosa in cystic fibrosis lungs. Alginate biosynthesis is controlled by a complex regulatory mechanism. Genes located in the 34-min region of the P. aeruginosa chromosome form an operon which encodes most of the biosynthetic enzymes necessary for alginate production. algD, the first gene in the operon and a critical point for the transcriptional regulation of alginate biosynthesis, is controlled by several trans, cis, and environmental factors. In this study, the involvement of the histone-like protein integration host factor (IHF) in algD expression was examined. Sequences with similarity to consensus IHF-binding sites of Escherichia coli were identified 75 bp upstream (site 1) and 90 bp downstream (site 2) of the start of algD transcription. In gel band mobility shift assays, DNA fragments containing either site bind IHF but site 2 has an approximately 90-fold higher affinity for IHF. Mutations in each of the elements were generated, and they resulted in the reduction or loss of in vitro IHF binding and a three- to fourfold decrease in algD-cat expression. This indicates that IHF binding is necessary for high-level algD transcription. The presence of a high-affinity IHF-binding site located 3' of the algD transcription start site suggested that sequences further downstream of this element are involved in algD expression. When a fragment located downstream of site 2 and upstream of the promoterless cat gene (+110 to +835) was deleted, algD-cat expression was reduced 10-fold supporting the notion that 3' enhancer elements are required for algD transcription. This is the first direct evidence of a 3' element involved in the control of a P. aeruginosa gene. It is postulated that IHF mediates the formation of a higher-order looped structure which is necessary for efficient algD transcription.
铜绿假单胞菌是免疫功能低下个体中一种极其重要的机会致病菌。从患有遗传性疾病囊性纤维化患者的慢性肺部感染中分离出的铜绿假单胞菌菌株具有黏液样菌落形态。这种表型是由于胞外多糖藻酸盐的过量产生,据信这赋予了铜绿假单胞菌在囊性纤维化肺部的选择性优势。藻酸盐生物合成受复杂的调控机制控制。位于铜绿假单胞菌染色体34分钟区域的基因形成一个操纵子,该操纵子编码藻酸盐产生所需的大部分生物合成酶。algD是操纵子中的第一个基因,也是藻酸盐生物合成转录调控的关键点,受多种反式、顺式和环境因素控制。在本研究中,检测了类组蛋白整合宿主因子(IHF)在algD表达中的作用。在algD转录起始点上游75 bp(位点1)和下游90 bp(位点2)处鉴定到与大肠杆菌共有IHF结合位点相似的序列。在凝胶迁移率变动分析中,包含任一位点的DNA片段都能结合IHF,但位点2对IHF的亲和力大约高90倍。对每个元件进行了突变,结果导致体外IHF结合减少或丧失,algD - cat表达降低三到四倍。这表明IHF结合对于高水平的algD转录是必要的。algD转录起始位点3'端存在高亲和力的IHF结合位点表明该元件下游的序列参与algD表达。当位于位点2下游和无启动子的cat基因上游(+110至+835)的片段被删除时,algD - cat表达降低了10倍,支持了3'增强子元件是algD转录所必需的观点。这是关于参与铜绿假单胞菌基因调控的3'元件的首个直接证据。据推测,IHF介导了高效algD转录所需的高阶环状结构的形成。