Department of Microbiology, Pusan National University, Busan 46241, Republic of Korea.
Microbiological Resource Research Institute, Pusan National University, Busan 46241, Republic of Korea.
RNA. 2021 Nov;27(11):1374-1389. doi: 10.1261/rna.078786.121. Epub 2021 Aug 24.
Toxin-antitoxin (TA) systems are genetic modules composed of a toxin interfering with cellular processes and its cognate antitoxin, which counteracts the activity of the toxin. TA modules are widespread in bacterial and archaeal genomes. It has been suggested that TA modules participate in the adaptation of prokaryotes to unfavorable conditions. The sp. PAMC 26642 used in this study was isolated from the Arctic lichen sp. There are 12 putative type II TA loci in the genome of sp. PAMC 26642. Of these, nine functional TA systems have been shown to be toxic in The toxin inhibits growth, but this inhibition is reversed when the cognate antitoxin genes are coexpressed, indicating that these putative TA loci were bona fide TA modules. Only the BoVapC1 (AXW83_01405) toxin, a homolog of VapC, showed growth inhibition specific to low temperatures, which was recovered by the coexpression of BoVapB1 (AXW83_01400). Microscopic observation and growth monitoring revealed that the BoVapC1 toxin had bacteriostatic effects on the growth of and induced morphological changes. Quantitative real time polymerase chain reaction and northern blotting analyses showed that the BoVapC1 toxin had a ribonuclease activity on the initiator tRNA, implying that degradation of tRNA might trigger growth arrest in Furthermore, the BoVapBC1 system was found to contribute to survival against prolonged exposure at 4°C. This is the first study to identify the function of TA systems in cold adaptation.
毒素-抗毒素 (TA) 系统是由一种干扰细胞过程的毒素及其同源抗毒素组成的基因模块,抗毒素可以中和毒素的活性。TA 模块广泛存在于细菌和古菌的基因组中。有人认为,TA 模块参与了原核生物对不利条件的适应。本研究中使用的 sp. PAMC 26642 是从北极地衣 sp. 中分离出来的。在 sp. PAMC 26642 的基因组中,有 12 个假定的 II 型 TA 基因座。其中,有 9 个功能性 TA 系统在 中被证明是有毒的。毒素抑制生长,但当共表达同源抗毒素基因时,这种抑制作用会被逆转,这表明这些假定的 TA 基因座是真正的 TA 模块。只有 BoVapC1 (AXW83_01405) 毒素,一种 VapC 的同源物,表现出对低温的特异性生长抑制,这种抑制作用可以通过 BoVapB1 (AXW83_01400) 的共表达来恢复。显微镜观察和生长监测表明,BoVapC1 毒素对 的生长具有抑菌作用,并诱导形态发生变化。定量实时聚合酶链反应和 northern blot 分析表明,BoVapC1 毒素对起始 tRNA 具有核糖核酸酶活性,这意味着 tRNA 的降解可能导致 的生长停滞。此外,还发现 BoVapBC1 系统有助于在 4°C 下长时间暴露时的存活。这是首次研究 TA 系统在冷适应中的功能。