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A LuxR-type regulator from Agrobacterium tumefaciens elevates Ti plasmid copy number by activating transcription of plasmid replication genes

机译:根癌农杆菌的LuxR型调节子通过激活质粒复制基因的转录来提高Ti质粒的拷贝数

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摘要

TraR, a LuxR-type quorum-sensing transcription factor in Agrobacterium tumefaciens , activates genes required for conjugal transfer of the Ti plasmid and also enhances the copy number of a nopaline-type Ti plasmid. Here, we show that TraR increases the copy number of an octopine-type Ti plasmid up to eightfold and that TraR activates transcription of the repABC operon up to 25-fold. The ability of TraR to increase copy number was strictly dependent on several TraR-activated promoters of this operon, indicating that TraR affects copy number solely at the level of transcription. Promoter resections and mRNA transcript analysis revealed the presence of three TraR-dependent promoters. Two TraR-dependent transcription start sites are located 45.5 and 65.5 nucleotides downstream of a site called tra box II, whereas the third start site lies 42.5 nucleotides downstream of a site called tra box III. Purified TraR bound to both tra boxes with comparable affinities, causing moderate DNA bending. TraR bound and bent these two sites independently rather than synergistically. Alteration of tra box III to match the consensus sequence dramatically increased TraR-dependent expression of repABC and plasmid copy number. TraR-dependent elevation of Ti plasmid copy number caused a three- to fourfold increase in plant tumorigenesis. [References: 41]
机译:TraR是根癌农杆菌中的LuxR型群体感应转录因子,它激活Ti质粒的结合转移所需的基因,并且还增加了胭脂碱型Ti质粒的拷贝数。在这里,我们显示TraR将章鱼碱型Ti质粒的拷贝数提高了八倍,并且TraR激活了repABC操纵子的转录达到了25倍。 TraR增加拷贝数的能力严格取决于该操纵子的几个TraR激活的启动子,表明TraR仅在转录水平上影响拷贝数。启动子切除和mRNA转录物分析揭示了三个TraR依赖性启动子的存在。两个TraR依赖性转录起始位点位于称为tra box II的位点下游45.5和65.5个核苷酸,而第三个起始位点位于称为tra box III的位点下游42.5个核苷酸。纯化的TraR以相似的亲和力与两个tra盒结合,导致中等的DNA弯曲。 TraR独立而非协同地约束和弯曲了这两个位点。 tra盒III的改变以匹配共有序列,从而显着增加了repABC的TraR依赖性表达和质粒拷贝数。 Ti质粒拷贝数的TraR依赖性升高导致植物肿瘤发生增加了三到四倍。 [参考:41]

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