Léon Grégory, Roy Paul H
Centre de Recherche en Infectiologie, Centre Hospitalier Universitaire de Québec, Québec, Québec, Canada.
J Bacteriol. 2009 Oct;191(19):6040-51. doi: 10.1128/JB.00674-09. Epub 2009 Jul 24.
Integrons are natural expression vectors in which gene cassettes are integrated downstream of a promoter region by a site-specific recombinase. Gene cassettes usually consist of a single gene followed by a recombination site designated attC. A major unanswered question is how a gene becomes associated with an attC site. Here, we investigate the potential role of a specific lineage of group IIC introns, named group IIC-attC, in cassette formation. Group IIC-attC introns preferentially target attC while retaining the ability to target transcriptional terminators. We show using a PCR-based mobility assay with Escherichia coli that the S.ma.I2 intron from the genome of a clinical isolate of Serratia marcescens can target both attC site and putative terminator motifs of resistance genes. Quantitative results showed that S.ma.I2 is more efficient in targeting various attC sequences than three group IIC-attC introns (54 to 64% sequence identity) from the genomes of environmental isolates. We also show that purified group IIC-attC intron-encoded reverse transcriptases have both RNA-dependent and DNA-dependent DNA polymerase activities in vitro. These data permit us to suggest a new model for gene cassette formation, in which a group IIC-attC intron targets separately a transcriptional terminator adjoining a gene and an isolated attC, joins the gene and the attC by homologous recombination, and then splices and reverse transcribes a gene-attC RNA template, leading to the formation of a cassette.
整合子是天然表达载体,基因盒通过位点特异性重组酶整合到启动子区域下游。基因盒通常由单个基因及其后的重组位点(称为attC)组成。一个主要未解决的问题是基因如何与attC位点相关联。在这里,我们研究了名为IIC-attC的IIC类内含子的特定谱系在盒式结构形成中的潜在作用。IIC-attC内含子优先靶向attC,同时保留靶向转录终止子的能力。我们使用基于PCR的迁移分析方法,以大肠杆菌为实验对象,证明了来自粘质沙雷氏菌临床分离株基因组的S.ma.I2内含子能够靶向attC位点和抗性基因的假定终止子基序。定量结果表明,与来自环境分离株基因组的三个IIC-attC内含子(序列同一性为54%至64%)相比,S.ma.I2在靶向各种attC序列方面效率更高。我们还表明,纯化的IIC-attC内含子编码的逆转录酶在体外具有RNA依赖性和DNA依赖性DNA聚合酶活性。这些数据使我们能够提出一种新的基因盒形成模型,即IIC-attC内含子分别靶向与基因相邻的转录终止子和孤立的attC,通过同源重组将基因和attC连接起来,然后剪接并逆转录基因-attC RNA模板,从而导致盒式结构的形成。