首页> 外文期刊>Journal of bacteriology >Analysis of the Ros repressor of Agrobacterium virC and virD operons: molecular intercommunication between plasmid and chromosomal genes.
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Analysis of the Ros repressor of Agrobacterium virC and virD operons: molecular intercommunication between plasmid and chromosomal genes.

机译:农杆菌virC和virD操纵子的Ros阻遏物分析:质粒和染色体基因之间的分子互通。

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The virulence genes of the Agrobacterium tumefaciens Ti plasmid are regulated both positively and negatively. The products of the genes of the virC and virD operons play an important role in host specificity and T-DNA processing. These operons are transcribed in opposite directions and therefore bear diametrically oriented promoters. These promoters are positively regulated by the VirG protein, which is believed to be activated through phosphorylation by a histidine kinase encoded by the virA gene. The virC and virD operons are also regulated by a 15.5-kDa repressor protein encoded by the ros chromosomal gene. A mutation in ros causes the constitutive expression of virC and virD in the complete absence of the VirG protein. It appears, therefore, that the Ros repressor interacts with the regulatory region of these operons. The Ros repressor is shown here to bind to an upstream sequence (Ros box) comprising 40 bp bearing a 9-bp inverted repeat, TATATTTCA/TGTAATATA, in the promoter region of these operons. The affinity for this sequence is specific and tenacious, since the addition of at least a 20,000-fold excess of competitor DNA failed to remove the Ros protein coding sequence from the Ros box. DNase I footprint analysis showed that the Ros box overlaps the binding site of VirG (Vir box). This result suggests that virC and virD transcription is modulated by Ros and VirG proteins.
机译:根癌农杆菌Ti质粒的毒力基因被正向和负向调节。 virC和virD操纵子基因的产物在宿主特异性和T-DNA加工中起重要作用。这些操纵子以相反的方向转录,因此带有沿直径方向的启动子。这些启动子受到VirG蛋白的正调控,该蛋白被认为是由virA基因编码的组氨酸激酶通过磷酸化激活的。 virC和virD操纵子也受ros染色体基因编码的15.5 kDa阻遏蛋白调节。 ros中的突变导致在完全不存在VirG蛋白的情况下virC和virD的组成型表达。因此,似乎罗斯阻遏物与这些操纵子的调控区相互作用。此处所示的Ros阻遏物在这些操纵子的启动子区域与上游序列(Ros box)结合,该上游序列包含40 bp,带有9 bp的反向重复序列TATATTTCA / TGTAATATA。该序列的亲和力是特异性和顽强的,因为添加了至少20,000倍过量的竞争者DNA未能从Ros盒中去除Ros蛋白编码序列。 DNase I足迹分析表明,Ros框与VirG(Vir框)的结合位点重叠。该结果表明,virC和virD转录受Ros和VirG蛋白调节。

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