Cellular and Molecular Microbiology (CM2), Faculté des Sciences, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Louvain Institute of Biomolecular Science and Technology, Université Catholique de Louvain (UCLouvain), Louvain-la-Neuve, Belgium.
mBio. 2020 Mar 31;11(2):e00452-20. doi: 10.1128/mBio.00452-20.
Much of the diversity of prokaryotic genomes is contributed by the tightly controlled recombination activity of transposons (Tns). The Tn family is arguably one of the most widespread transposon families. Members carry a large range of passenger genes incorporated into their structures. Family members undergo replicative transposition using a DDE transposase to generate a cointegrate structure which is then resolved by site-specific recombination between specific DNA sequences () on each of the two Tn copies in the cointegrate. These sites also carry promoters controlling expression of the recombinase and transposase. We report here that a number of Tn members encode a type II toxin-antitoxin (TA) system, typically composed of a stable toxin and a labile antitoxin that binds the toxin and inhibits its lethal activity. This system serves to improve plasmid maintenance in a bacterial population and, until recently, was believed to be associated with bacterial persistence. At least six different TA gene pairs are associated with various Tn members. Our data suggest that several independent acquisition events have occurred. In contrast to most Tn family passenger genes, which are generally located away from the transposition module, the TA gene pairs abut the site upstream of the resolvase genes. Although their role when part of Tn family transposons is unclear, this finding suggests a potential role for the embedded TA in stabilizing the associated transposon with the possibility that TA expression is coupled to expression of transposase and resolvase during the transposition process itself. Transposable elements (TEs) are important in genetic diversification due to their recombination properties and their ability to promote horizontal gene transfer. Over the last decades, much effort has been made to understand TE transposition mechanisms and their impact on prokaryotic genomes. For example, the Tn family is ubiquitous in bacteria, molding their host genomes by the paste-and-copy mechanism. In addition to the transposition module, Tn members often carry additional passenger genes (e.g., conferring antibiotic or heavy metal resistance and virulence), and three were previously known to carry a toxin-antitoxin (TA) system often associated with plasmid maintenance; however, the role of TA systems within the Tn family is unknown. The genetic context of TA systems in Tn members suggests that they may play a regulatory role in ensuring stable invasion of these Tns during transposition.
原核生物基因组的多样性在很大程度上是由转座子(Tn)的严格控制的重组活性贡献的。Tn 家族可以说是最广泛的转座子家族之一。成员携带大量乘客基因,这些基因被整合到它们的结构中。家族成员使用 DDE 转座酶进行复制转座,产生一个共整合体结构,然后通过共整合体中两个 Tn 拷贝上的特定 DNA 序列()之间的位点特异性重组来解决。这些位点还携带控制重组酶和转座酶表达的启动子。我们在这里报告,许多 Tn 成员编码一种 II 型毒素-抗毒素(TA)系统,通常由一个稳定的毒素和一个不稳定的抗毒素组成,该抗毒素结合毒素并抑制其致死活性。该系统有助于提高细菌群体中质粒的维持率,直到最近,人们还认为它与细菌的持久性有关。至少有六个不同的 TA 基因对与各种 Tn 成员相关。我们的数据表明,发生了几次独立的获得事件。与大多数远离转座模块的 Tn 家族乘客基因不同,TA 基因对位于整合酶基因上游的 位点附近。虽然它们作为 Tn 家族转座子的一部分的作用尚不清楚,但这一发现表明,嵌入 TA 在稳定相关转座子方面可能具有潜在作用,并且 TA 的表达可能与转座酶和整合酶在转座过程本身中的表达相关联。转座元件(TEs)由于其重组特性及其促进水平基因转移的能力,在遗传多样化中起着重要作用。在过去的几十年中,人们做出了很大的努力来理解 TE 转座机制及其对原核生物基因组的影响。例如,Tn 家族在细菌中无处不在,通过粘贴和复制机制塑造宿主基因组。除了转座模块外,Tn 成员通常还携带额外的乘客基因(例如,赋予抗生素或重金属抗性和毒力),并且之前有三个已知携带毒素-抗毒素(TA)系统,通常与质粒维持有关;然而,Tn 家族中 TA 系统的作用尚不清楚。Tn 成员中 TA 系统的遗传背景表明,它们可能在确保这些 Tn 在转座过程中稳定入侵方面发挥调节作用。