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农杆菌virC和virD操纵子的Ros阻遏物分析:质粒与染色体基因之间的分子相互作用

Analysis of the Ros repressor of Agrobacterium virC and virD operons: molecular intercommunication between plasmid and chromosomal genes.

作者信息

D'Souza-Ault M R, Cooley M B, Kado C I

机构信息

Department of Plant Pathology, University of California, Davis 95616.

出版信息

J Bacteriol. 1993 Jun;175(11):3486-90. doi: 10.1128/jb.175.11.3486-3490.1993.

Abstract

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.

摘要

根癌土壤杆菌Ti质粒的毒力基因受到正向和负向调控。virC和virD操纵子基因的产物在宿主特异性和T-DNA加工过程中发挥重要作用。这些操纵子以相反方向转录,因此具有完全相反的启动子。这些启动子受到VirG蛋白的正向调控,据信VirG蛋白通过由virA基因编码的组氨酸激酶磷酸化而被激活。virC和virD操纵子也受到ros染色体基因编码的15.5 kDa阻遏蛋白的调控。ros基因突变会导致在完全没有VirG蛋白的情况下virC和virD组成型表达。因此看来,Ros阻遏蛋白与这些操纵子的调控区域相互作用。本文显示Ros阻遏蛋白与这些操纵子启动子区域中一个包含40 bp的上游序列(Ros框)结合,该序列带有一个9 bp的反向重复序列TATATTTCA/TGTAATATA。对该序列的亲和力具有特异性且很强,因为加入至少20000倍过量的竞争DNA也无法从Ros框中去除Ros蛋白编码序列。DNase I足迹分析表明Ros框与VirG的结合位点(Vir框)重叠。这一结果表明virC和virD的转录受到Ros和VirG蛋白的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79fc/204748/6098968fd4b8/jbacter00053-0254-a.jpg

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