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转录干扰和抑制调节了费氏中华根瘤菌共生质粒的接合能力。

Transcriptional interference and repression modulate the conjugative ability of the symbiotic plasmid of Rhizobium etli.

作者信息

Sepúlveda Edgardo, Pérez-Mendoza Daniel, Ramírez-Romero Miguel A, Soto María J, López-Lara Isabel M, Geiger Otto, Sanjuán Juan, Brom Susana, Romero David

机构信息

Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Apartado Postal 565-A, Cuernavaca, Morelos, México.

出版信息

J Bacteriol. 2008 Jun;190(12):4189-97. doi: 10.1128/JB.00041-08. Epub 2008 Apr 18.

Abstract

Bacteria of the order Rhizobiales are able to establish nitrogen-fixing symbioses with legumes. Commonly, genes for symbiosis are harbored on large symbiotic plasmids. Although the transfer of symbiotic plasmids is commonly detected in nature, there are few experimentally characterized examples. In Rhizobium etli, the product of rctA inhibits the conjugation of the symbiotic plasmid by reducing the transcription of the virB operon. rctA is transcribed divergently from this operon, and its product is predicted to have a DNA binding domain. In the present study, using DNase I footprinting and binding assays, we demonstrated the specific binding of RctA to the virB operon promoter. A 9-bp motif in the spacer region of this promoter (the rctA binding motif box) and the presence of a functional -10 region were critical elements for RctA binding. Transcriptional fusion analyses revealed that the elimination of either element provoked a relief of RctA-mediated repression. These data support a model in which RctA inhibits the access of the RNA polymerase to the virB promoter. Interestingly, rctA expression levels were modulated by transcriptional interference from transcripts emanating from the virB promoter. This phenomenon adds another level of regulation for this system, thus revealing a novel mechanism of plasmid transfer regulation in the Rhizobiales.

摘要

根瘤菌目细菌能够与豆科植物建立固氮共生关系。通常,共生基因位于大型共生质粒上。虽然在自然界中通常能检测到共生质粒的转移,但经过实验表征的例子很少。在费氏中华根瘤菌中,rctA的产物通过降低virB操纵子的转录来抑制共生质粒的接合。rctA与该操纵子反向转录,其产物预计具有一个DNA结合结构域。在本研究中,我们使用DNA酶I足迹法和结合试验,证明了RctA与virB操纵子启动子的特异性结合。该启动子间隔区中的一个9碱基基序(rctA结合基序框)和一个功能性 -10区域的存在是RctA结合的关键元件。转录融合分析表明,消除任何一个元件都会导致RctA介导的抑制作用解除。这些数据支持了一个模型,即RctA抑制RNA聚合酶与virB启动子的结合。有趣的是,rctA的表达水平受到来自virB启动子转录本的转录干扰的调节。这种现象为该系统增加了另一个调控层次,从而揭示了根瘤菌目质粒转移调控的一种新机制。

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