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噬菌体 PhiKZ 非病毒 RNA 聚合酶的结构。

Structure of the bacteriophage PhiKZ non-virion RNA polymerase.

机构信息

Section for Structural and Synthetic Biology, Department of Infectious Disease, Imperial College London, London, UK.

Peter the Great St. Petersburg Polytechnic University, St. Petersburg, Russia.

出版信息

Nucleic Acids Res. 2021 Jul 21;49(13):7732-7739. doi: 10.1093/nar/gkab539.

Abstract

Bacteriophage ΦKZ (PhiKZ) is the archetype of a family of massive bacterial viruses. It is considered to have therapeutic potential as its host, Pseudomonas aeruginosa, is an opportunistic, intrinsically antibiotic resistant, pathogen that kills tens of thousands worldwide each year. ΦKZ is an incredibly interesting virus, expressing many systems that the host already possesses. On infection, it forms a 'nucleus', erecting a barrier around its genome to exclude host endonucleases and CRISPR-Cas systems. ΦKZ infection is independent of the host transcriptional apparatus. It expresses two different multi-subunit RNA polymerases (RNAPs): the virion RNAP (vRNAP) is injected with the viral DNA during infection to transcribe early genes, including those encoding the non-virion RNAP (nvRNAP), which transcribes all further genes. ΦKZ nvRNAP is formed by four polypeptides thought to represent homologues of the eubacterial β/β' subunits, and a fifth with unclear homology, but essential for transcription. We have resolved the structure of ΦKZ nvRNAP to better than 3.0 Å, shedding light on its assembly, homology, and the biological role of the fifth subunit: it is an embedded, integral member of the complex, the position, structural homology and biochemical role of which imply that it has evolved from an ancestral homologue to σ-factor.

摘要

噬菌体 ΦKZ(PhiKZ)是一类巨型细菌病毒的原型。由于其宿主铜绿假单胞菌是一种机会性、固有抗药性、能导致每年全球数以万计人死亡的病原体,因此被认为具有治疗潜力。ΦKZ 是一种非常有趣的病毒,它表达了宿主已经拥有的许多系统。感染时,它形成一个“核”,在其基因组周围竖起一道屏障,以排除宿主内切酶和 CRISPR-Cas 系统。ΦKZ 感染不依赖于宿主转录装置。它表达两种不同的多亚基 RNA 聚合酶(RNAP):病毒 RNA 聚合酶(vRNAP)在感染过程中与病毒 DNA 一起被注射,以转录早期基因,包括编码非病毒 RNA 聚合酶(nvRNAP)的基因,nvRNAP 转录所有进一步的基因。ΦKZ nvRNAP 由四个假定代表真细菌β/β'亚基同源物的多肽和一个同源性不明但对转录至关重要的第五个多肽组成。我们已经将 ΦKZ nvRNAP 的结构解析到 3.0Å 以上,这揭示了它的组装、同源性以及第五个亚基的生物学作用:它是复合物的嵌入式整体成员,其位置、结构同源性和生化作用表明它是从祖先同源物进化而来的 σ 因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ad/8287921/a414ba6f96cf/gkab539fig1.jpg

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