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A non-canonical multisubunit RNA polymerase encoded by a giant bacteriophage

机译:巨型噬菌体编码的非规范性多亚基RNA聚合酶

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The infection of Pseudomonas aeruginosa by the giant bacteriophage phiKZ is resistant to host RNA polymerase (RNAP) inhibitor rifampicin. phiKZ encodes two sets of polypeptides that are distantly related to fragments of the two largest subunits of cellular multisubunit RNAPs. Polypeptides of one set are encoded by middle phage genes and are found in the phiKZ virions. Polypeptides of the second set are encoded by early phage genes and are absent from virions. Here, we report isolation of a five-subunit RNAP from phiKZ-infected cells. Four subunits of this enzyme are cellular RNAP subunits homologs of the non-virion set; the fifth subunit is a protein of unknown function. In vitro, this complex initiates transcription from late phiKZ promoters in rifampicin-resistant manner. Thus, this enzyme is a non-virion phiKZ RNAP responsible for transcription of late phage genes. The phiKZ RNAP lacks identifiable assembly and promoter specificity subunits/factors characteristic for eukaryal, archaeal and bacterial RNAPs and thus provides a unique model for comparative analysis of the mechanism, regulation and evolution of this important class of enzymes.
机译:巨大的噬菌体phiKZ感染铜绿假单胞菌对宿主RNA聚合酶(RNAP)抑制剂利福平有抗性。 phiKZ编码两组与细胞多亚基RNAP的两个最大亚基的片段紧密相关的多肽。一组多肽由中间噬菌体基因编码,并在phiKZ病毒粒子中发现。第二组多肽由早期噬菌体基因编码,病毒体中不存在。在这里,我们报告从phiKZ感染的细胞中分离出5个亚基的RNAP。该酶的四个亚基是非病毒体组的细胞RNAP亚基的同源物。第五亚基是功能未知的蛋白质。在体外,该复合物以耐利福平的方式从晚期phiKZ启动子启动转录。因此,该酶是负责晚期噬菌体基因转录的非病毒体phiKZ RNAP。 phiKZ RNAP缺乏针对真核,古细菌和细菌RNAP的可识别的组装和启动子特异性亚基/因子,因此为比较分析这种重要酶的机制,调控和进化提供了独特的模型。

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