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毒素-抗毒素系统:生物学、鉴定及应用

Toxin-antitoxin systems: Biology, identification, and application.

作者信息

Unterholzner Simon J, Poppenberger Brigitte, Rozhon Wilfried

机构信息

1 Biotechnology of Horticultural Crops; Technische Universität München; Freising, Germany.

出版信息

Mob Genet Elements. 2013 Sep 1;3(5):e26219. doi: 10.4161/mge.26219. Epub 2013 Aug 20.

DOI:10.4161/mge.26219
PMID:24251069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3827094/
Abstract

Toxin-antitoxin (TA) systems are small genetic elements composed of a toxin gene and its cognate antitoxin. The toxins of all known TA systems are proteins while the antitoxins are either proteins or non-coding RNAs. Based on the molecular nature of the antitoxin and its mode of interaction with the toxin the TA modules are currently grouped into five classes. In general, the toxin is more stable than the antitoxin but the latter is expressed to a higher level. If supply of the antitoxin stops, for instance under special growth conditions or by plasmid loss in case of plasmid encoded TA systems, the antitoxin is rapidly degraded and can no longer counteract the toxin. Consequently, the toxin becomes activated and can act on its cellular targets. Typically, TA toxins act on crucial cellular processes including translation, replication, cytoskeleton formation, membrane integrity, and cell wall biosynthesis. TA systems and their components are also versatile tools for a multitude of purposes in basic research and biotechnology. Currently, TA systems are frequently used for selection in cloning and for single protein expression in living bacterial cells. Since several TA toxins exhibit activity in yeast and mammalian cells they may be useful for applications in eukaryotic systems. TA modules are also considered as promising targets for the development of antibacterial drugs and their potential to combat viral infection may aid in controlling infectious diseases.

摘要

毒素-抗毒素(TA)系统是由毒素基因及其同源抗毒素组成的小遗传元件。所有已知TA系统的毒素都是蛋白质,而抗毒素则是蛋白质或非编码RNA。根据抗毒素的分子性质及其与毒素的相互作用方式,TA模块目前分为五类。一般来说,毒素比抗毒素更稳定,但抗毒素的表达水平更高。如果抗毒素的供应停止,例如在特殊生长条件下或在质粒编码的TA系统中因质粒丢失,抗毒素会迅速降解,不再能对抗毒素。因此,毒素被激活并可作用于其细胞靶点。通常,TA毒素作用于关键的细胞过程,包括翻译、复制、细胞骨架形成、膜完整性和细胞壁生物合成。TA系统及其组件也是基础研究和生物技术中用于多种目的的通用工具。目前,TA系统经常用于克隆筛选和在活细菌细胞中进行单一蛋白质表达。由于几种TA毒素在酵母和哺乳动物细胞中表现出活性,它们可能对真核系统中的应用有用。TA模块也被认为是开发抗菌药物的有前景的靶点,并且它们对抗病毒感染的潜力可能有助于控制传染病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/da2341faef2b/mge-3-e26219-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/dd7f9b4eb69f/mge-3-e26219-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/90a2033c3cc6/mge-3-e26219-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/23bf0fc69ef1/mge-3-e26219-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/fedcc287a5a2/mge-3-e26219-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/d525ec55603f/mge-3-e26219-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/da2341faef2b/mge-3-e26219-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/dd7f9b4eb69f/mge-3-e26219-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/90a2033c3cc6/mge-3-e26219-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/23bf0fc69ef1/mge-3-e26219-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/fedcc287a5a2/mge-3-e26219-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/d525ec55603f/mge-3-e26219-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/346b/3827094/da2341faef2b/mge-3-e26219-g6.jpg

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