噬菌体 PhiKZ 非病毒 RNA 聚合酶从其启动子 p119L 转录的结构。

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2024-07-17 DOI:10.1016/j.jmb.2024.168713
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引用次数: 0

摘要

噬菌体ΦKZ(phiKZ)是巨型细菌病毒家族的创始成员。它具有治疗潜力,因为其宿主铜绿假单胞菌每年导致全球数万人死亡。ΦKZ 的感染不受宿主转录装置的影响;病毒形成一个 "核",在 ΦKZ 基因组周围形成一个蛋白屏障,将宿主免疫系统排除在外。它表达自己的非典型多亚基非病毒 RNA 聚合酶(nvRNAP),并将其输入 "核",以转录病毒基因。ΦKZ nvRNAP由四种多肽组成,分别代表真细菌β/β'亚基的同源物,第五种多肽可能是从σ-因子的祖先同源物进化而来。我们解析了从其同源启动子 p119L 启动转录的 ΦKZ nvRNAP 的结构,包括以前紊乱的结构域和区域。我们的研究结果揭示了ΦKZ nvRNAP转录机制与典型的真菌RNAP和相关的噬菌体AR9的非典型nvRNAP转录机制之间的异同。
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Structure of the Bacteriophage PhiKZ Non-virion RNA Polymerase Transcribing from its Promoter p119L

Bacteriophage ΦKZ (PhiKZ) is the founding member of a family of giant bacterial viruses. It has potential as a therapeutic as its host, Pseudomonas aeruginosa, kills tens of thousands of people worldwide each year. ΦKZ infection is independent of the host transcriptional apparatus; the virus forms a “nucleus”, producing a proteinaceous barrier around the ΦKZ genome that excludes the host immune systems. It expresses its own non-canonical multi-subunit non-virion RNA polymerase (nvRNAP), which is imported into its “nucleus” to transcribe viral genes. The ΦKZ nvRNAP is formed by four polypeptides representing homologues of the eubacterial β/β′ subunits, and a fifth that is likely to have evolved from an ancestral homologue to σ-factor. We have resolved the structure of the ΦKZ nvRNAP initiating transcription from its cognate promoter, p119L, including previously disordered regions. Our results shed light on the similarities and differences between ΦKZ nvRNAP mechanisms of transcription and those of canonical eubacterial RNAPs and the related non-canonical nvRNAP of bacteriophage AR9.

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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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