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Characterization of a novel toxin-antitoxin module, VapBC, encoded by Leptospira interrogans chromosome

机译:钩端螺旋体染色体编码的新型毒素-抗毒素模块VapBC的表征

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Comparative genomic analysis of the coding sequences (CDSs) of Leptospira interrogans revealed a pair of closely linked genes homologous to the vapBC loci of many other bacteria with respect to both deduced amino acid sequences and operon organizations. Expression of single vapC gene in Escherichia coli resulted in inhibition of bacterial growth, whereas co-expression of vapBC restored the growth effectively. This phenotype is typical for three other characterized toxin-antitoxin systems of bacteria,i.e., mazEF[1], relBE[2] and chpIK[3]. The VapC proteins of bacteria and a thermophilic archeae, Solfolobus tokodaii, form a structurally distinguished group of toxin different from the other known toxins of bacteria. Phylogenetic analysis of both toxins and antitoxins of all categories indicated that although toxins were evolved from divergent sources and may or may not follow their speciation paths (as indicated by their 16s RNA sequences), co-evolution with their antitoxins was obvious.
机译:对问号钩端螺旋体编码序列(CDSs)的比较基因组分析表明,在推导的氨基酸序列和操纵子组织方面,一对与许多其他细菌的vapBC基因座同源的紧密连接的基因。单个vapC基因在大肠杆菌中的表达导致细菌生长的抑制,而vapBC的共表达有效地恢复了生长。该表型是细菌的其他三个特征性毒素-抗毒素系统的典型表型,即mazEF [1],relBE [2]和chpIK [3]。细菌和嗜热古菌Solfolobus tokodaii的VapC蛋白形成了结构上独特的一组毒素,与其他已知的细菌毒素不同。对所有类别毒素和抗毒素的系统进化分析表明,尽管毒素是从不同的来源进化而来的,可能也可能不遵循其物种形成路径(如其16s RNA序列所示),但与它们的抗毒素共同进化是显而易见的。

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