Delany Isabel, Spohn Gunther, Rappuoli Rino, Scarlato Vincenzo
Department of Molecular Biology, IRIS, Chiron SpA, Via Fiorentina 1, 53100 Siena, Italy.
J Bacteriol. 2002 Sep;184(17):4800-10. doi: 10.1128/JB.184.17.4800-4810.2002.
Helicobacter pylori encodes three two-component systems and two orphan response regulators (RRs) that are predicted to be involved in transcriptional regulation. The HP1043 gene encodes an essential OmpR-like RR, 1043RR, for which no histidine kinase has been identified. Gel filtration and cross-linking experiments on the purified 1043RR protein reveals that this protein is a dimer and in vivo dimerization assays localize the dimerization to the N-terminal regulatory domain. DNA-binding studies have revealed two targets for specific binding of the 1043RR protein and moreover, phosphorylation of the protein was not needed for the activation of binding. Footprinting analysis demonstrated that the 1043RR protein binds to its own promoter, P(1043), overlapping the -35 promoter element from positions -17 to -45, suggesting that this protein is autoregulatory. In addition, it binds at a similar location, spanning nucleotides from positions -22 to -51 at the promoter of the methyl-accepting chemotaxis tlpB gene, P(tlpB). A possible inverted repeat was identified in the binding sites of both promoters. In an attempt to overexpress 1043RR in H. pylori, the 10-fold induction in transcription of a second copy of HP1043 with use of an inducible promoter failed to increase cellular levels of the RR protein, suggesting that 1043RR is tightly regulated at a posttranscriptional level. The P(1043) and P(tlpB) promoters were demonstrated to be coordinately regulated in response to growth phase in H. pylori. The essential role of HP1043 in encoding a cell cycle regulator is discussed.
幽门螺杆菌编码三个双组分系统和两个孤儿应答调节因子(RRs),预计它们参与转录调控。HP1043基因编码一种必需的类OmpR应答调节因子1043RR,尚未鉴定出与之对应的组氨酸激酶。对纯化的1043RR蛋白进行的凝胶过滤和交联实验表明,该蛋白是二聚体,体内二聚化分析将二聚化定位到N端调节结构域。DNA结合研究揭示了1043RR蛋白特异性结合的两个靶点,此外,该蛋白的磷酸化对于结合的激活不是必需的。足迹分析表明,1043RR蛋白与其自身的启动子P(1043)结合,从-17到-45位与-35启动子元件重叠,这表明该蛋白具有自调节作用。此外,它在类似位置结合,跨越甲基接受趋化性tlpB基因启动子P(tlpB)上从-22到-51位的核苷酸。在两个启动子的结合位点中鉴定出一个可能的反向重复序列。为了在幽门螺杆菌中过表达1043RR,使用诱导型启动子对HP1043的第二个拷贝进行转录10倍诱导未能增加RR蛋白的细胞水平,这表明1043RR在转录后水平受到严格调控。已证明P(1043)和P(tlpB)启动子在幽门螺杆菌中响应生长阶段而受到协同调控。讨论了HP1043在编码细胞周期调节因子中的重要作用。