VIB-VUB Center for Structural Biology, Vrije Universiteit Brussel and Vlaams Instituut voor Biotechnologie, Brussels, Belgium.
Protein Sci. 2021 Jun;30(6):1103-1113. doi: 10.1002/pro.4071. Epub 2021 Apr 7.
Toxin-antitoxin (TA) modules are small operons in bacteria and archaea that encode a metabolic inhibitor (toxin) and a matching regulatory protein (antitoxin). While their biochemical activities are often well defined, their biological functions remain unclear. In Type II TA modules, the most common class, both toxin and antitoxin are proteins, and the antitoxin inhibits the biochemical activity of the toxin via complex formation with the toxin. The different TA modules vary significantly regarding structure and biochemical activity. Both regulation of protein activity by the antitoxin and regulation of transcription can be highly complex and sometimes show striking parallels between otherwise unrelated TA modules. Interplay between the multiple levels of regulation in the broader context of the cell as a whole is most likely required for optimum fine-tuning of these systems. Thus, TA modules can go through great lengths to prevent activation and to reverse accidental activation, in agreement with recent in vivo data. These complex mechanisms seem at odds with the lack of a clear biological function.
毒素-抗毒素 (TA) 模块是细菌和古菌中的小操纵子,它们编码代谢抑制剂(毒素)和匹配的调节蛋白(抗毒素)。尽管它们的生化活性通常定义明确,但它们的生物学功能仍不清楚。在 II 型 TA 模块中,最常见的一类,毒素和抗毒素都是蛋白质,抗毒素通过与毒素形成复合物来抑制毒素的生化活性。不同的 TA 模块在结构和生化活性方面差异很大。抗毒素对蛋白质活性的调节和转录的调节都可能非常复杂,有时在 otherwise unrelated TA 模块之间显示出惊人的相似之处。在整个细胞的更广泛背景下,多个调节水平的相互作用可能是对这些系统进行最佳微调所必需的。因此,TA 模块可以采取各种措施来防止激活和逆转意外激活,这与最近的体内数据一致。这些复杂的机制似乎与缺乏明确的生物学功能不一致。