Department of Applied Life Sciences, Niigata University of Pharmacy and Applied Life Sciences, Niigata, Japan.
RNA Biol. 2012 Dec;9(12):1520-7. doi: 10.4161/rna.22757. Epub 2012 Nov 6.
Toxin-antitoxin (TA) systems are categorized into three classes based on the type of antitoxin. In type I TA systems, the antitoxin is a small antisense RNA that inhibits translation of small toxic proteins by binding to the corresponding mRNAs. Those type I TA systems were originally identified as plasmid stabilization modules rendering a post-segregational killing (PSK) effect on the host cells. The type I TA loci also exist on the Escherichia coli chromosome but their biological functions are less clear. Genetic organization and regulatory elements of hok/sok and ldr/rdl families are very similar and the toxins are predicted to contain a transmembrane domain, but otherwise share no detectable sequence similarity. This review will give an overview of the type I TA modules of E. coli K-12, especially hok/sok, ldr/rdl and SOS-inducible symE/symR systems, which are regulated by divergently overlapping cis-encoded antisense RNAs.
毒素-抗毒素 (TA) 系统根据抗毒素的类型分为三类。在 I 型 TA 系统中,抗毒素是一种小的反义 RNA,通过与相应的 mRNA 结合来抑制小毒性蛋白的翻译。这些 I 型 TA 系统最初被鉴定为质粒稳定模块,对宿主细胞产生了继分离杀伤 (PSK) 效应。I 型 TA 基因座也存在于大肠杆菌染色体上,但它们的生物学功能不太清楚。hok/sok 和 ldr/rdl 家族的遗传组织和调节元件非常相似,预测毒素含有一个跨膜结构域,但除此之外,没有检测到可检测的序列相似性。本综述将概述大肠杆菌 K-12 的 I 型 TA 模块,特别是 hok/sok、ldr/rdl 和 SOS 诱导的 symE/symR 系统,这些系统受顺式编码反义 RNA 的重叠调控。