Abstract

Toxin-antitoxin (TA) systems are found in nearly all prokaryotic genomes and usually consist of a pair of co-transcribed genes, one of which encodes a stable toxin and the other, its cognate labile antitoxin. Certain environmental and physiological cues trigger the degradation of the antitoxin, causing activation of the toxin, leading either to the death or stasis of the host cell. TA systems have a variety of functions in the bacterial cell, including acting as mediators of programmed cell death, the induction of a dormant state known as persistence and the stable maintenance of plasmids and other mobile genetic elements. Some bacterial TA systems are functional when expressed in eukaryotic cells and this has led to several innovative applications, which are the subject of this review. Here, we look at how bacterial TA systems have been utilized for the genetic manipulation of yeasts and other eukaryotes, for the containment of genetically modified organisms, and for the engineering of high expression eukaryotic cell lines. We also examine how TA systems have been adopted as an important tool in developmental biology research for the ablation of specific cells and the potential for utility of TA systems in antiviral and anticancer gene therapies.

Highlights

  • IntroductionToxin-antitoxin (TA) systems are nearly ubiquitous genetic modules in bacterial and archaeal genomes

  • An Overview of Bacterial Toxin-Antitoxin SystemsToxin-antitoxin (TA) systems are nearly ubiquitous genetic modules in bacterial and archaeal genomes

  • Toxins 2016, 8, 49 these TA-encoding plasmids and TA systems were termed as addiction modules [6,7]. Chromosomal homologues of these plasmid-encoded addiction modules were first reported in Escherichia coli and the chromosomal mazEF system, comprising the mazE-encoded antitoxin and the mazF-encoded toxin, was postulated to mediate programmed bacterial cell death under nutrient starvation conditions [8]

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Summary

Introduction

Toxin-antitoxin (TA) systems are nearly ubiquitous genetic modules in bacterial and archaeal genomes. Chromosomal homologues of these plasmid-encoded addiction modules were first reported in Escherichia coli and the chromosomal mazEF system, comprising the mazE-encoded antitoxin and the mazF-encoded toxin, was postulated to mediate programmed bacterial cell death under nutrient starvation conditions [8] This apparent altruistic killing was envisaged to enable part of the bacterial population to survive during adverse conditions, reflecting a multicellular facet of bacteria [8,9,10]. A potentially new class of TA system (a possible type VI) was recently discovered in the form of the SocAB system from Caulobacter crescentus [29] Both the SocB toxin and the SocA antitoxin are proteins but in this case, the SocB toxin is the unstable partner due to its susceptibility to the endogenous ClpXP protease. In this mini-review, we will look at several strategies used for the heterologous expression of bacterial TA genes in eukaryotic systems and their potential applications in biotechnology and molecular biology

TA Systems as Tools for Containment in Yeasts
TA Systems as Tools for the Genetic Manipulation of Yeasts
Cell Ablation for the Containment of Genetically Modified Plants
Cell Ablation in Developmental Biology Research of Higher Eukaryotes
Antiviral Gene Therapy
Anticancer Gene Therapy
Conclusions
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