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集胞藻 PCC 6803 大型防御质粒 pSYSA 上的毒素-抗毒素系统。

Toxin-antitoxin systems on the large defense plasmid pSYSA of Synechocystis sp. PCC 6803.

机构信息

Faculty of Biology, University of Freiburg, Schänzlestrasse 1, D-79104 Freiburg, Germany.

出版信息

J Biol Chem. 2013 Mar 8;288(10):7399-409. doi: 10.1074/jbc.M112.434100. Epub 2013 Jan 15.

Abstract

Bacterial toxin-antitoxin (TA) systems are genetic elements, which are encoded by plasmid as well as chromosomal loci and mediate plasmid and genomic island maintenance through post-segregational killing mechanisms. TA systems exist in surprisingly high numbers in all prokaryotes, but cyanobacterial TA systems have been only very poorly experimentally characterized so far. Cyanobacteria are the only prokaryotes that perform oxygenic photosynthesis. As such, cyanobacteria are of high ecological importance and are considered promising for the production of biofuels. Here, we present the molecular characterization of the sll7003/ssl7004 TA system encoded on plasmid pSYSA of the model cyanobacterium Synechocystis sp. PCC 6803 as involving a Mg(2+)-dependent RNA endonuclease activity targeting single-stranded RNA regions and demonstrate the functionality of four more TA systems encoded on this 100,749-bp plasmid. Furthermore, one additional type I, one additional type II, and three freestanding TA system components are predicted on pSYSA, all of which appear active judged by their expression. By harboring at least seven simultaneously active TA systems, pSYSA appears as the plasmid most strongly selected for among all plasmids studied in this respect thus far. These results point to a high biological relevance of pSYSA, whose coding capacity is 75% devoted to three distinct clustered regularly interspaced short palindromic repeats (CRISPR) systems mediating antiviral defense.

摘要

细菌毒素-抗毒素(TA)系统是遗传元件,由质粒和染色体基因座编码,并通过继代杀伤机制介导质粒和基因组岛的维持。TA 系统在所有原核生物中都存在惊人的高数量,但迄今为止,蓝藻 TA 系统仅得到了非常有限的实验表征。蓝藻是唯一进行有氧光合作用的原核生物。因此,蓝藻具有很高的生态重要性,并被认为是生产生物燃料的有前途的生物。在这里,我们介绍了模型蓝藻集胞藻 6803 的质粒 pSYSA 上编码的 sll7003/ssl7004 TA 系统的分子特征,该系统涉及靶向单链 RNA 区域的 Mg2+依赖性 RNA 内切酶活性,并证明了该质粒上编码的另外四个 TA 系统的功能。此外,pSYSA 上预测了一个额外的 I 型、一个额外的 II 型和三个独立的 TA 系统组件,根据它们的表达情况,所有这些组件似乎都具有活性。由于至少有七个同时活跃的 TA 系统,pSYSA 似乎是迄今为止在这方面研究的所有质粒中被选择最强的质粒。这些结果表明 pSYSA 具有很高的生物学相关性,其编码能力有 75%用于三个不同的簇状规则间隔短回文重复(CRISPR)系统,介导抗病毒防御。

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