Julian Daniel J, Kershaw Christopher J, Brown Nigel L, Hobman Jon L
School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Antonie Van Leeuwenhoek. 2009 Aug;96(2):149-59. doi: 10.1007/s10482-008-9293-4. Epub 2008 Nov 13.
Metal responsive MerR family transcriptional regulators are widespread in bacteria and activate the transcription of genes involved in metal ion detoxification, efflux, or homeostasis, in response to the presence of cognate metal species in the cytoplasm. MerR family regulators recognize and bind to dyad symmetrical DNA sequences in specific promoters that have a spacer region between the -35 and -10 sequences which is longer than the canonical 16-18 bp spacer for other sigma(70)-dependent promoters. In this study we report beta-galactosidase assays of MerR family-regulated gene expression in the multiple metal resistant bacterium Cupriavidus metallidurans. A series of pMU2385 reporter plasmid derivatives containing cloned MerR family-activated promoters were used to determine metal ion-induced responses from different MerR family regulated promoters, as well as regulators cloned with the cognate promoter into pMU2385. Mercuric ion-responsive MerR and lead ion-responsive PbrR activity was confirmed using this assay system as well as MerR family activator activity on heterologous promoters PcopA, PcadA, and Pzcc from Escherichia coli, Pseudomonas aeruginosa and Bordetella pertussis, respectively. In C. metallidurans CH34, transcription from these promoters was activated by MerR family regulators encoded on the chromosome or megaplasmids in response to copper (PcopA), and lead (PcadA and PzccA), showing that MerR family activators in C. metallidurans can act on MerR family promoters from other organisms, which have sequence differences to the predicted C. metallidurans promoters.
金属响应性MerR家族转录调节因子在细菌中广泛存在,可响应细胞质中同源金属物种的存在,激活参与金属离子解毒、外排或稳态的基因转录。MerR家族调节因子识别并结合特定启动子中的二元对称DNA序列,这些启动子在-35和-10序列之间有一个间隔区,该间隔区比其他依赖σ⁷⁰的启动子的标准16 - 18 bp间隔区长。在本研究中,我们报告了在多重金属抗性细菌金属贪铜菌中对MerR家族调节的基因表达进行的β - 半乳糖苷酶测定。一系列含有克隆的MerR家族激活启动子的pMU2385报告质粒衍生物用于确定不同MerR家族调节启动子的金属离子诱导反应,以及与同源启动子一起克隆到pMU2385中的调节因子。使用该测定系统证实了汞离子响应性MerR和铅离子响应性PbrR的活性,以及MerR家族激活剂分别对来自大肠杆菌、铜绿假单胞菌和百日咳博德特氏菌的异源启动子PcopA、PcadA和Pzcc的活性。在金属贪铜菌CH34中,这些启动子的转录由染色体或大质粒上编码的MerR家族调节因子激活,以响应铜(PcopA)和铅(PcadA和PzccA),表明金属贪铜菌中的MerR家族激活剂可以作用于其他生物体的MerR家族启动子,这些启动子与预测的金属贪铜菌启动子存在序列差异。