Kreusch D, von Lintig J, Schröder J
Institut für Biologie II, Universität Freiburg, Germany.
Mol Gen Genet. 1995 Nov 1;249(1):102-10. doi: 10.1007/BF00290241.
The occ and noc regions in octopine and nopaline Ti plasmids, respectively, are responsible for the catabolism of octopine and nopaline in Agrobacterium. The functions are activated in the presence of the opines by OccR and NocR, two related regulatory proteins, and the promoters contain common sequence motifs. We have investigated heterologous interactions between the regulators and the promoters. Previous experiments using all possible heterologous combinations of opines, regulators, and promoters in vivo had demonstrated that only the combination of nopaline, NocR, and the occ promoter led to limited promoter activation. We now show that OccR and NocR bind to the heterologous promoters in vitro and in vivo. The weak or non-existent promoter activation actually observed could be explained by the assumption that OccR and NocR use different activation mechanisms; we investigated protein-induced DNA bending because of reports that the two regulators differ in this respect. Analysis with a bending vector showed that both OccR and NocR induced a DNA bend that is relaxed in the presence of the respective opine. The data suggest that subtle differences in regulator/promoter interactions are responsible for the inactivity of the heterologous combinations. Investigations with a chimeric NocR/OccR protein indicated that it induced a DNA bend in both promoters. No opine-induced relaxation was detectable with the hybrid, and the inducible promoter was not activated. These findings suggest that bend relaxation may be an integral part of promoter activation.
章鱼碱型和胭脂碱型Ti质粒中的章鱼碱和胭脂碱区域(分别为occ和noc区域)负责根癌土壤杆菌中章鱼碱和胭脂碱的分解代谢。在章鱼碱型调节蛋白OccR和胭脂碱型调节蛋白NocR这两种相关调节蛋白存在的情况下,这些功能会被激活,并且启动子含有共同的序列基序。我们研究了调节蛋白与启动子之间的异源相互作用。之前在体内使用所有可能的章鱼碱、调节蛋白和启动子的异源组合进行的实验表明,只有胭脂碱、NocR和occ启动子的组合导致有限的启动子激活。我们现在表明,OccR和NocR在体外和体内均能与异源启动子结合。实际观察到的弱启动子激活或无启动子激活现象可以通过OccR和NocR使用不同激活机制这一假设来解释;由于有报道称这两种调节蛋白在这方面存在差异,我们研究了蛋白质诱导的DNA弯曲。用弯曲载体进行的分析表明,OccR和NocR均诱导了DNA弯曲,并且在各自的章鱼碱存在时这种弯曲会松弛。数据表明,调节蛋白/启动子相互作用中的细微差异是异源组合无活性的原因。对嵌合NocR/OccR蛋白的研究表明,它在两个启动子中均诱导了DNA弯曲。对于该杂交蛋白,未检测到章鱼碱诱导的松弛现象,并且可诱导启动子未被激活。这些发现表明,弯曲松弛可能是启动子激活的一个组成部分。