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首页> 外文期刊>RNA >VapC6, a ribonucleolytic toxin regulates thermophilicity in the crenarchaeote Sulfolobus solfataricus.
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VapC6, a ribonucleolytic toxin regulates thermophilicity in the crenarchaeote Sulfolobus solfataricus.

机译:VapC6是一种核糖核酸分解毒素,可调节Crenarchaeote Sulfolobus solfataricus中的嗜热性。

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摘要

The phylum Crenarchaeota includes hyperthermophilic micro-organisms subjected to dynamic thermal conditions. Previous transcriptomic studies of Sulfolobus solfataricus identified vapBC6 as a heat-shock (HS)-inducible member of the Vap toxin-antitoxin gene family. In this study, the inactivation of the vapBC6 operon by targeted gene disruption produced two recessive phenotypes related to fitness, HS sensitivity and a heat-dependent reduction in the rate of growth. In-frame vapBC6 deletion mutants were analyzed to examine the respective roles of each protein. Since vapB6 transcript abundance was elevated in the vapC6 deletion, the VapC6 toxin appears to regulate abundance of its cognate antitoxin. In contrast, vapC6 transcript abundance was reduced in the vapB6 deletion. A putative intergenic terminator may underlie these observations by coordinating vapBC6 expression. As predicted by structural modeling, recombinant VapC6 produced using chaperone cosynthesis exhibited heat-dependent ribonucleolytic activity toward S. solfataricus total RNA. This activity could be blocked by addition of preheated recombinant VapB6. In vivo transcript targets were identified by assessing the relative expression of genes that naturally respond to thermal stress in VapBC6-deficient cells. Preferential increases were observed for dppB-1 and tetR, and preferential decreases were observed for rpoD and eIF2 gamma. Specific VapC6 ribonucleolytic action could also be demonstrated in vitro toward RNAs whose expression increased in the VapBC6-deficient strain during heat shock. These findings provide a biochemical mechanism and identify cellular targets underlying VapBC6-mediated control over microbial growth and survival at temperature extremes.
机译:Crenarchaeota门包括经受动态热条件的超嗜热微生物。以前的Sulfolobus solfataricus的转录组学研究表明,vapBC6是Vap毒素-抗毒素基因家族的热休克(HS)诱导型成员。在这项研究中,有针对性的基因破坏使vapBC6操纵子失活,产生了两种隐性表型,与适应性,HS敏感性和热依赖性生长速率的降低有关。分析了框内vapBC6缺失突变体,以检查每种蛋白质的各自作用。由于在vapC6缺失中vapB6转录物的丰度提高了,因此VapC6毒素似乎可以调节其相关抗毒素的丰度。相反,vapB6缺失减少了vapC6转录本的丰度。推定的基因间终止子可能通过协调vapBC6表达而成为这些观察的基础。如通过结构模型预测的那样,使用分子伴侣共生产生的重组VapC6对S. solfataricus总RNA表现出热依赖性的核糖核酸分解活性。可以通过添加预热的重组VapB6来阻止此活性。通过评估在VapBC6缺陷细胞中自然响应热应激的基因的相对表达,鉴定了体内转录目标。观察到dppB-1和tetR优先升高,而rpoD和eIF2γ优先降低。还可以在体外针对热休克期间在VapBC6缺陷型菌株中表达增加的RNA表现出特异性的VapC6核糖核酸分解作用。这些发现提供了一种生化机制,并确定了在极端温度下VapBC6介导的微生物生长和存活控制基础的细胞靶标。

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