Foster T J, Ginnity F
J Bacteriol. 1985 May;162(2):773-6. doi: 10.1128/jb.162.2.773-776.1985.
Transcription of the mer genes of plasmid R100 is regulated by the product of the merR gene. The merR gene negatively regulates its own expression and also controls the transcription of the merTCA operon both negatively (in the absence of inducer) and positively (in the presence of inducer). We used transcriptional mer-lac fusions of R100-1 in complementation tests to measure the ability of the merR products of different mercury-resistant transposons and plasmids to functionally interact with R100-1. Plasmids from incompatibility groups C, B, S, L, and P, as well as the Pseudomonas transposons Tn501 and Tn3401, regulated the expression of the R100 mer genes in a similar fashion to the R100-1 merR product itself, suggesting that these elements are closely related. Only plasmid R391 (IncJ) did not complement.
质粒R100的mer基因转录受merR基因产物调控。merR基因对自身表达起负调控作用,同时对merTCA操纵子的转录在无诱导物时起负调控作用,在有诱导物时起正调控作用。我们在互补试验中使用R100 - 1的转录mer - lac融合体来测定不同耐汞转座子和质粒的merR产物与R100 - 1功能相互作用的能力。来自不相容群C、B、S、L和P的质粒,以及假单胞菌转座子Tn501和Tn3401,对R100 mer基因表达的调控方式与R100 - 1的merR产物本身相似,这表明这些元件密切相关。只有质粒R391(IncJ)不能互补。