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金黄色葡萄球菌RNAIII通过反义机制协同抑制毒力因子和转录调节因子Rot的合成。

Staphylococcus aureus RNAIII coordinately represses the synthesis of virulence factors and the transcription regulator Rot by an antisense mechanism.

作者信息

Boisset Sandrine, Geissmann Thomas, Huntzinger Eric, Fechter Pierre, Bendridi Nadia, Possedko Maria, Chevalier Clément, Helfer Anne Catherine, Benito Yvonne, Jacquier Alain, Gaspin Christine, Vandenesch François, Romby Pascale

机构信息

Institut National pour la Recherche Médicale INSERM E0230, Université Lyon 1, Centre National de Référence des Staphylocoques, Faculté Laennec, Lyon, F-69008, France.

出版信息

Genes Dev. 2007 Jun 1;21(11):1353-66. doi: 10.1101/gad.423507.

Abstract

RNAIII is the intracellular effector of the quorum-sensing system in Staphylococcus aureus. It is one of the largest regulatory RNAs (514 nucleotides long) that are known to control the expression of a large number of virulence genes. Here, we show that the 3' domain of RNAIII coordinately represses at the post-transcriptional level, the expression of mRNAs that encode a class of virulence factors that act early in the infection process. We demonstrate that the 3' domain acts primarily as an antisense RNA and rapidly anneals to these mRNAs, forming long RNA duplexes. The interaction between RNAIII and the mRNAs results in repression of translation initiation and triggers endoribonuclease III hydrolysis. These processes are followed by rapid depletion of the mRNA pool. In addition, we show that RNAIII and its 3' domain mediate translational repression of rot mRNA through a limited number of base pairings involving two loop-loop interactions. Since Rot is a transcriptional regulatory protein, we proposed that RNAIII indirectly acts on many downstream genes, resulting in the activation of the synthesis of several exoproteins. These data emphasize the multitude of regulatory steps affected by RNAIII and its 3' domain in establishing a network of S. aureus virulence factors.

摘要

RNAIII是金黄色葡萄球菌群体感应系统的细胞内效应分子。它是已知的最大调控RNA之一(长度为514个核苷酸),可控制大量毒力基因的表达。在此,我们表明RNAIII的3'结构域在转录后水平协同抑制一类在感染过程早期起作用的毒力因子编码mRNA的表达。我们证明3'结构域主要作为反义RNA发挥作用,并迅速与这些mRNA退火,形成长RNA双链体。RNAIII与mRNA之间的相互作用导致翻译起始受到抑制,并触发核糖核酸酶III水解。这些过程随后导致mRNA池的快速消耗。此外,我们表明RNAIII及其3'结构域通过涉及两个环-环相互作用的有限数量碱基配对介导rot mRNA的翻译抑制。由于Rot是一种转录调节蛋白,我们推测RNAIII间接作用于许多下游基因,导致几种外毒素合成的激活。这些数据强调了RNAIII及其3'结构域在建立金黄色葡萄球菌毒力因子网络中影响的众多调控步骤。

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