Idola Desmila, Mori Hiroshi, Nagata Yuji, Nonaka Lisa, Yano Hirokazu
Graduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, Aobaku, Sendai, 980-8577, Japan.
Department of Informatics, National Institute of Genetics, 1111 Yata, Mishima, 411-8540, Japan.
Mob DNA. 2023 May 26;14(1):7. doi: 10.1186/s13100-023-00295-5.
The strand-biased circularizing integrative elements (SEs) are putatively non-mobilizable integrative elements for transmitting antimicrobial resistance genes. The transposition mode and the prevalence of SEs in prokaryotes remain vague.
To corroborate the transposition mode and the prevalence of SEs, hypothetical transposition intermediates of an SE were searched for in genomic DNA fractions of an SE host. Then, the SE core genes were defined based on gene knockout experiments, and the synteny blocks of their distant homologs were searched for in the RefSeq complete genome sequence database using PSI-BLAST. A genomic DNA fractionation experiment revealed that SE copies are present in a double-stranded nicked circular form in vivo. Operonic structure of three conserved coding sequences (intA, tfp, intB) and srap located at the left end of SEs were identified as essential for attL × attR recombination. The synteny blocks of tfp and srap homologs were detected in 3.6% of the replicons of Gammaproteobacteria but not in other taxa, implying that SE movement is host-dependent. SEs have been discovered most frequently in the orders Vibrionales (19% of replicons), Pseudomonadales (18%), Alteromonadales (17%), and Aeromonadales (12%). Genomic comparisons revealed 35 new SE members with identifiable termini. SEs are present at 1 to 2 copies per replicon and have a median length of 15.7 kb. Three newly identified SE members carry antimicrobial resistance genes, like tmexCD-toprJ, mcr-9, and bla. Further experiments validated that three new SE members possess the strand-biased attL × attR recombination activity.
This study suggested that transposition intermediates of SEs are double-stranded circular DNA. The main hosts of SEs are a subset of free-living Gammaproteobacteria; this represents a rather narrow host range compared to those of mobile DNA element groups discovered to date. As the host range, genetic organization, and movements are unique among the mobile DNA elements, SEs provide a new model system for host-mobile DNA element coevolution studies.
链偏向性环化整合元件(SEs)被认为是用于传递抗菌抗性基因的不可移动整合元件。SEs在原核生物中的转座模式和流行情况仍不明确。
为了证实SEs的转座模式和流行情况,在SE宿主的基因组DNA片段中搜索SE的假设转座中间体。然后,基于基因敲除实验定义SE核心基因,并使用PSI-BLAST在RefSeq完整基因组序列数据库中搜索其远缘同源物的同线性模块。基因组DNA分级分离实验表明,SE拷贝在体内以双链带切口的环状形式存在。位于SEs左端的三个保守编码序列(intA、tfp、intB)和srap的操纵子结构被确定为attL×attR重组所必需。在3.6%的γ-变形菌纲复制子中检测到tfp和srap同源物的同线性模块,但在其他分类群中未检测到,这意味着SE的移动是宿主依赖性的。SEs在弧菌目(19%的复制子)、假单胞菌目(18%)、交替单胞菌目(17%)和气单胞菌目(12%)中最常被发现。基因组比较揭示了35个具有可识别末端的新SE成员。SEs在每个复制子中以1至2个拷贝存在,中位数长度为15.7 kb。三个新鉴定的SE成员携带抗菌抗性基因,如tmexCD-toprJ/mcr-9和bla。进一步的实验证实,三个新的SE成员具有链偏向性attL×attR重组活性。
本研究表明,SEs的转座中间体是双链环状DNA。SEs的主要宿主是自由生活的γ-变形菌纲的一个子集;与迄今发现的移动DNA元件组相比,这代表了一个相当狭窄的宿主范围。由于宿主范围、遗传组织和移动在移动DNA元件中是独特的,SEs为宿主-移动DNA元件共同进化研究提供了一个新的模型系统。