Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide, Consejo Superior de Investigaciones Científicas, Junta de Andalucía, Seville, Spain.
J Bacteriol. 2012 Dec;194(23):6560-73. doi: 10.1128/JB.01348-12. Epub 2012 Oct 5.
The atzS-atzT-atzU-atzV-atzW gene cluster of the Pseudomonas sp. strain ADP atrazine-degradative plasmid pADP-1, which carries genes for an outer membrane protein and the components of a putative ABC-type solute transporter, is located downstream from atzR, which encodes the LysR-type transcriptional regulator of the cyanuric acid-degradative operon atzDEF. Here we describe the transcriptional organization of these genes. Our results show that all six genes are cotranscribed from the PatzR promoter to form the atzRSTUVW operon. A second, stronger promoter, PatzT, is found within atzS and directs transcription of the four distal genes. PatzT is σ(N) dependent, activated by NtrC in response to nitrogen limitation with the aid of IHF, and repressed by AtzR. A combination of in vivo mutational analysis and primer extension allowed us to locate the PatzT promoter and map the transcriptional start site. Similarly, we used deletion and point mutation analyses, along with in vivo expression studies and in vitro binding assays, to locate the NtrC, IHF, and AtzR binding sites and address their functionality. Our results suggest a regulatory model in which NtrC activates PatzT transcription via DNA looping, while AtzR acts as an antiactivator that diminishes expression by interfering with the activation process.
ADP 菌株 Pseudomonas sp. 菌株的 atzS-atzT-atzU-atzV-atzW 基因簇是 atzR 下游的位置,该基因簇位于 atrazine 降解质粒 pADP-1 上,编码氰尿酸降解操纵子 atzDEF 的 LysR 型转录调节因子。这里我们描述了这些基因的转录组织。我们的结果表明,所有六个基因都从 PatzR 启动子共转录形成 atzRSTUVW 操纵子。在 atzS 内发现了第二个更强的启动子 PatzT,它指导四个远端基因的转录。PatzT 依赖于 σ(N),在氮限制下 NtrC 通过 IHF 激活,并且受到 AtzR 的抑制。体内突变分析和引物延伸的组合使我们能够定位 PatzT 启动子并绘制转录起始位点。同样,我们使用缺失和点突变分析,以及体内表达研究和体外结合测定,定位 NtrC、IHF 和 AtzR 结合位点并解决它们的功能。我们的结果表明了一种调节模型,其中 NtrC 通过 DNA 环化激活 PatzT 转录,而 AtzR 作为反激活因子通过干扰激活过程来降低表达。