首页> 美国卫生研究院文献>Journal of Bacteriology >Transposable Modules Generated by a Single Copy of Insertion Sequence ISPme1 and Their Influence on Structure and Evolution of Natural Plasmids of Paracoccus methylutens DM12
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Transposable Modules Generated by a Single Copy of Insertion Sequence ISPme1 and Their Influence on Structure and Evolution of Natural Plasmids of Paracoccus methylutens DM12

机译:插入序列ISPme1的单个副本生成的转座模块及其对甲基副球菌DM12天然质粒的结构和进化的影响。

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摘要

We demonstrated that a single copy of insertion sequence ISPme1 can mobilize adjacent segments of genomic DNA of Paracoccus methylutens DM12, which leads to the generation of diverse transposable elements of various size and DNA contents. All elements (named transposable modules [TMos]) contain ISPme1 (placed at the 5′ ends of the elements) and have variable 3′-end regions of between 0.5 and 5 kb. ISPme1 was shown to encode an outwardly oriented promoter, which may activate the transcription of genes transposed within TMos in evolutionarily distinct hosts. TMos may therefore be considered to be natural systems enabling gene capture, expression, and spread. However, unless these elements have been inserted into a highly conserved genetic context to enable a precise definition of their termini, it is extremely difficult or even impossible to identify them in bacterial genomes by in silico sequence analysis. We showed that TMos are present in the chromosome and plasmids of strain DM12. Sequence analysis of plasmid pMTH1 (32 kb) revealed that four TMos, previously identified with a trap vector, pMEC1, comprise 87% of its genome. Repeated TMos within pMTH1 may stimulate other structural rearrangements resulting from homologous recombination between long repeat sequences. This illustrates that TMos may play a significant role in shaping the structure of natural plasmids, which consequently may have a great impact on the evolution of plasmid genomes.
机译:我们证明了插入序列ISPme1的单个副本可以动员甲基副球菌DM12基因组DNA的相邻片段,从而导致产生各种大小和DNA含量的多种转座因子。所有元素(命名为转座模块[TMos])都包含ISPme1(位于元素的5'末端),并具有介于0.5到5 kb之间的可变3'末端区域。已显示ISPme1编码向外定向的启动子,该启动子可能激活在进化上不同的宿主中TMos内转座的基因的转录。因此,TMos可以被认为是能够进行基因捕获,表达和扩散的天然系统。但是,除非将这些元件插入高度保守的遗传环境中以能够对其末端进行精确定义,否则通过计算机序列分析在细菌基因组中鉴定它们非常困难,甚至不可能。我们表明TMos存在于菌株DM12的染色体和质粒中。质粒pMTH1(32 kb)的序列分析表明,先前用捕获载体pMEC1鉴定的四个TMos占其基因组的87%。 pMTH1中重复的TMos可能会刺激长重复序列之间同源重组导致的其他结构重排。这说明TMos可能在塑造天然质粒的结构中起重要作用,因此可能对质粒基因组的进化产生重大影响。

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