Attaiech Laetitia, Boughammoura Aïda, Brochier-Armanet Céline, Allatif Omran, Peillard-Fiorente Flora, Edwards Ross A, Omar Ayat R, MacMillan Andrew M, Glover Mark, Charpentier Xavier
CNRS UMR5240, Microbiologie Adaptation et Pathogénie, 69622 Villeurbanne, France; Université Claude Bernard Lyon 1, 69100 Villeurbanne, France; International Center for Infectiology Research (CIRI), International Center for Infectiology Research, Université de Lyon, 69364 Lyon, France; INSERM U1111, 69364 Lyon, France; Ecole Normale Supérieure de Lyon, 69364 Lyon, France; Université Claude Bernard Lyon 1, Centre International de Recherche en Infectiologie, 69364 Lyon, France; CNRS UMR5308, 69007 Lyon, France;
CNRS UMR5240, Microbiologie Adaptation et Pathogénie, 69622 Villeurbanne, France; Université Claude Bernard Lyon 1, 69100 Villeurbanne, France;
Proc Natl Acad Sci U S A. 2016 Aug 2;113(31):8813-8. doi: 10.1073/pnas.1601626113. Epub 2016 Jul 18.
A highly conserved DNA uptake system allows many bacteria to actively import and integrate exogenous DNA. This process, called natural transformation, represents a major mechanism of horizontal gene transfer (HGT) involved in the acquisition of virulence and antibiotic resistance determinants. Despite evidence of HGT and the high level of conservation of the genes coding the DNA uptake system, most bacterial species appear non-transformable under laboratory conditions. In naturally transformable species, the DNA uptake system is only expressed when bacteria enter a physiological state called competence, which develops under specific conditions. Here, we investigated the mechanism that controls expression of the DNA uptake system in the human pathogen Legionella pneumophila We found that a repressor of this system displays a conserved ProQ/FinO domain and interacts with a newly characterized trans-acting sRNA, RocR. Together, they target mRNAs of the genes coding the DNA uptake system to control natural transformation. This RNA-based silencing represents a previously unknown regulatory means to control this major mechanism of HGT. Importantly, these findings also show that chromosome-encoded ProQ/FinO domain-containing proteins can assist trans-acting sRNAs and that this class of RNA chaperones could play key roles in post-transcriptional gene regulation throughout bacterial species.
一种高度保守的DNA摄取系统使许多细菌能够主动摄取并整合外源DNA。这一过程称为自然转化,是水平基因转移(HGT)的主要机制之一,参与毒力和抗生素抗性决定因素的获得。尽管有水平基因转移的证据以及编码DNA摄取系统的基因具有高度保守性,但在实验室条件下,大多数细菌物种似乎都不可转化。在自然可转化的物种中,DNA摄取系统仅在细菌进入一种称为感受态的生理状态时才表达,感受态在特定条件下形成。在此,我们研究了人类病原体嗜肺军团菌中控制DNA摄取系统表达的机制。我们发现该系统的一个阻遏物具有保守的ProQ/FinO结构域,并与一种新鉴定的反式作用小RNA(RocR)相互作用。它们共同靶向编码DNA摄取系统的基因的mRNA,以控制自然转化。这种基于RNA的沉默代表了一种此前未知的调控方式,用于控制这种主要的水平基因转移机制。重要的是,这些发现还表明,染色体编码的含ProQ/FinO结构域的蛋白质可以协助反式作用小RNA,并且这类RNA伴侣可能在整个细菌物种的转录后基因调控中发挥关键作用。