Li Zhen, Song Qinghao, Wang Yinzhao, Xiao Xiang, Xu Jun
State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Institute of Oceanography, Shanghai Jiao Tong University, Shanghai, China.
Extremophiles. 2018 May;22(3):347-357. doi: 10.1007/s00792-018-1002-2. Epub 2018 Jan 15.
Toxin-antitoxin (TA) system is bacterial or archaeal genetic module consisting of toxin and antitoxin gene that be organized as a bicistronic operon. TA system could elicit programmed cell death, which is supposed to play important roles for the survival of prokaryotic population under various physiological stress conditions. The phage abortive infection system (AbiE family) belongs to bacterial type IV TA system. However, no archaeal AbiE family TA system has been reported so far. In this study, a putative AbiE TA system (PygAT), which is located in a genomic island PYG1 in the chromosome of Pyrococcus yayanosii CH1, was identified and characterized. In Escherichia coli, overexpression of the toxin gene pygT inhibited its growth while the toxic effect can be suppressed by introducing the antitoxin gene pygA in the same cell. PygAT also enhances the stability of shuttle plasmids with archaeal plasmid replication protein Rep75 in E. coli. In P. yayanosii, disruption of antitoxin gene pygA cause a significantly growth delayed under high hydrostatic pressure (HHP). The antitoxin protein PygA can specifically bind to the PygAT promoter region and regulate the transcription of pygT gene in vivo. These results show that PygAT is a functional TA system in P. yayanosii, and also may play a role in the adaptation to HHP environment.
毒素-抗毒素(TA)系统是细菌或古菌的遗传模块,由毒素基因和抗毒素基因组成,二者作为一个双顺反子操纵子排列。TA系统可引发程序性细胞死亡,这被认为在各种生理应激条件下对原核生物群体的生存起着重要作用。噬菌体流产感染系统(AbiE家族)属于细菌IV型TA系统。然而,迄今为止尚未报道过古菌AbiE家族TA系统。在本研究中,鉴定并表征了一个假定的AbiE TA系统(PygAT),其位于嗜压热球菌CH1染色体上的基因组岛PYG1中。在大肠杆菌中,毒素基因pygT的过表达抑制其生长,而在同一细胞中引入抗毒素基因pygA可抑制这种毒性作用。PygAT还增强了大肠杆菌中携带古菌质粒复制蛋白Rep75的穿梭质粒的稳定性。在嗜压热球菌中,抗毒素基因pygA的破坏导致在高静水压(HHP)下生长显著延迟。抗毒素蛋白PygA可特异性结合PygAT启动子区域并在体内调节pygT基因的转录。这些结果表明,PygAT是嗜压热球菌中的一个功能性TA系统,也可能在适应HHP环境中发挥作用。