Takaya Akiko, Watanabe Masato, Yamamoto Tomoko
Department of Microbiology and Molecular Genetics, Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, 263-8522, Japan.
Antimicrob Agents Chemother. 2006 Apr;50(4):1143-7. doi: 10.1128/AAC.50.4.1143-1147.2006.
Transposon Tn2610, found in a conjugative plasmid from an Escherichia coli isolate recovered at a hospital in Chiba, Japan, in 1975, was completely sequenced. Tn2610 is 23,883 bp long and is bracketed by two transposition modules, a Tn1721-like module and a Tn21-derived module, which correspond, respectively, to the long inverted repeats IRa and IRb previously described for this transposon. Although both tnpA genes are intact, only that in the Tn21-derived module (IRb) functions in the transposition, while that in the Tn1721-derived module (IRa) cannot recognize the 38-bp imperfect repeat at the end of the IRb element. Both tnpR and res are present in IRa, while the tnpR gene of IRb is interrupted by the insertion of an IS26 insertion element. The intervening region, between the res site of the Tn1721 module and IS26, carries multiple integron-associated resistance genes within a Tn21 backbone, including a region identical to that found in the genome of Salmonella enterica serovar Typhimurium DT104. These findings suggest that Tn2610 originated from Tn1721 and Tn21, with extensive recombination events with other elements which have resulted in a complex mosaic structure.
转座子Tn2610于1975年在日本千叶一家医院分离出的大肠杆菌的接合性质粒中被发现,其全序列已测定。Tn2610长23,883 bp,两侧为两个转座模块,一个Tn1721样模块和一个Tn21衍生模块,它们分别对应于先前针对该转座子描述的长反向重复序列IRa和IRb。虽然两个tnpA基因都是完整的,但只有Tn21衍生模块(IRb)中的那个在转座中起作用,而Tn1721衍生模块(IRa)中的那个不能识别IRb元件末端的38 bp不完全重复序列。tnpR和res都存在于IRa中,而IRb的tnpR基因因IS26插入元件的插入而中断。Tn1721模块的res位点与IS26之间的间隔区域在Tn21主链内携带多个与整合子相关的抗性基因,包括与肠炎沙门氏菌血清型鼠伤寒DT104基因组中发现的区域相同的区域。这些发现表明Tn2610起源于Tn1721和Tn21,并与其他元件发生了广泛的重组事件,从而形成了复杂的镶嵌结构。