Department of Virology and Microbiology, Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), Instituto de Biología Molecular "Eladio Viñuela" (CSIC), C. Nicolás Cabrera 1, Universidad Autónoma, Canto Blanco, 28049 Madrid, Spain.
Centro de Investigaciones Biológicas (CSIC), Ramiro de Maeztu 9, 28040 Madrid, Spain.
Nucleic Acids Res. 2018 Dec 14;46(22):11910-11926. doi: 10.1093/nar/gky996.
The principal route for dissemination of antibiotic resistance genes is conjugation by which a conjugative DNA element is transferred from a donor to a recipient cell. Conjugative elements contain genes that are important for their establishment in the new host, for instance by counteracting the host defense mechanisms acting against incoming foreign DNA. Little is known about these establishment genes and how they are regulated. Here, we deciphered the regulation mechanism of possible establishment genes of plasmid p576 from the Gram-positive bacterium Bacillus pumilus. Unlike the ssDNA promoters described for some conjugative plasmids, the four promoters of these p576 genes are repressed by a repressor protein, which we named Reg576. Reg576 also regulates its own expression. After transfer of the DNA, these genes are de-repressed for a period of time until sufficient Reg576 is synthesized to repress the promoters again. Complementary in vivo and in vitro analyses showed that different operator configurations in the promoter regions of these genes lead to different responses to Reg576. Each operator is bound with extreme cooperativity by two Reg576-dimers. The X-ray structure revealed that Reg576 has a Ribbon-Helix-Helix core and provided important insights into the high cooperativity of DNA recognition.
抗生素耐药基因传播的主要途径是通过接合,其中一个可接合的 DNA 元件从供体转移到受体细胞。可接合元件包含对其在新宿主中建立非常重要的基因,例如通过抵消针对外来 DNA 的宿主防御机制。关于这些建立基因以及它们如何被调控的信息知之甚少。在这里,我们破译了革兰氏阳性芽孢杆菌芽孢杆菌质粒 p576 中可能的建立基因的调控机制。与一些可接合质粒中描述的 ssDNA 启动子不同,这些 p576 基因的四个启动子受一种称为 Reg576 的抑制蛋白抑制。Reg576 还调控其自身的表达。在 DNA 转移后,这些基因在一段时间内解除抑制,直到合成足够的 Reg576 再次抑制启动子。互补的体内和体外分析表明,这些基因启动子中的不同操纵子构型导致对 Reg576 的不同反应。每个操纵子都被两个 Reg576-二聚体以极端协同性结合。X 射线结构揭示了 Reg576 具有一个 Ribbon-Helix-Helix 核心,并为 DNA 识别的高协同性提供了重要的见解。