Caigoy Jant Cres, Shimamoto Toshi, Ishida Yojiro, Ahmed Ashraf M, Miyoshi Shin-Ichi, Shimamoto Tadashi
Laboratory of Food Microbiology and Hygiene, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Japan.
Department of Structural Biology, Protein Technologies Center, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Microbiol Immunol. 2025 Jan;69(1):1-9. doi: 10.1111/1348-0421.13181. Epub 2024 Nov 18.
Bacterial reverse transcriptase coding gene (RT) is essential for the production of a small satellite DNA-RNA complex called multicopy single-stranded DNA (msDNA). In this study, we found a novel retron, retron-Vmi1 (Vm85) from Vibrio mimicus. The retron is comprised of the msr-msd region, orf323, and the ret gene, a genetic organization similar to Salmonella's retron-Sen2 (St85). The protein sequence of the RNA-directed DNA polymerase (RT-Vmi1) is highly homologous to the RTs of Vibrio metoecus, Vibrio parahaemolyticus, and Vibrio vulnificus. Phylogenetic and protein sequence similarity analysis of retron-Vmi1 ORF323 and RT revealed a close relatedness to retron-Sen2. We found that retron-Vmi1 was inserted in the dusA gene, similar to the insertion of the retron-Vpa1 (Vp96) of V. parahaemolyticus AQ3354, suggesting that retrons can be transferred via the tRNA gene. These results are the first convincing evidence that retron is moving across species. The neighboring genes of retron-Vmi1 shared high homology with the genetic environment of V. parahaemolyticus and V. vulnificus retrons. We also found two junction points within the retron-Vmi1 and the dusA gene suggesting that retron-Vmi1 was inserted into this site in a two-step manner.
细菌逆转录酶编码基因(RT)对于一种名为多拷贝单链DNA(msDNA)的小卫星DNA - RNA复合物的产生至关重要。在本研究中,我们从模仿弧菌中发现了一种新型反转录子,即反转录子 - Vmi1(Vm85)。该反转录子由msr - msd区域、orf323和ret基因组成,其基因组织类似于沙门氏菌的反转录子 - Sen2(St85)。RNA指导的DNA聚合酶(RT - Vmi1)的蛋白质序列与梅氏弧菌、副溶血性弧菌和创伤弧菌的RT高度同源。对反转录子 - Vmi1的ORF323和RT进行系统发育和蛋白质序列相似性分析,发现其与反转录子 - Sen2密切相关。我们发现反转录子 - Vmi1插入到dusA基因中,类似于副溶血性弧菌AQ3354的反转录子 - Vpa1(Vp96)的插入,这表明反转录子可以通过tRNA基因进行转移。这些结果是反转录子跨物种转移的首个令人信服的证据。反转录子 - Vmi1的相邻基因与副溶血性弧菌和创伤弧菌反转录子的遗传环境具有高度同源性。我们还在反转录子 - Vmi1和dusA基因内发现了两个连接点,这表明反转录子 - Vmi1是以两步方式插入到该位点的。