Eugene V Koonin, Matthias G Fischer, Jens H Kuhn, Mart Krupovic
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Related to polintoviricetes are vertebrate adenovirids; unclassified polinton-like viruses (PLVs) identified in various environments or integrated into diverse protist genomes; virophages (<i>Maveriviricetes</i>), which are part of tripartite hyperparasitic systems including protist hosts and giant viruses; and capsid-less derivatives, such as cytoplasmic linear DNA plasmids of fungi and transpovirons. Phylogenomic analysis indicates that the polinton-like supergroup of viruses bridges bacterial tectivirids (preplasmiviricot class <i>Tectiliviricetes</i>) to the phylum <i>Nucleocytoviricota</i> that includes large and giant eukaryotic DNA viruses. Comparative structural analysis of proteins encoded by polinton-like viruses led to the discovery of previously undetected functional domains, such as terminal proteins and distinct proteases implicated in DNA polymerase processing, and clarified the evolutionary relationships within <i>Polintoviricetes</i>. Here, we leverage these insights into the evolution of the polinton-like supergroup to develop an amended megataxonomy that groups <i>Polintoviricetes</i>, PLVs (new class '<i>Aquintoviricetes</i>'), and virophages (renamed class '<i>Virophaviricetes</i>') together with <i>Adenoviridae</i> (new class '<i>Pharingeaviricetes</i>') in a preplasmiviricot subphylum '<i>Polisuviricotina</i>' sister to a subphylum including <i>Tectiliviricetes</i> ('<i>Prepoliviricotina</i>').</p>","PeriodicalId":18520,"journal":{"name":"Microbiology and Molecular Biology Reviews","volume":null,"pages":null},"PeriodicalIF":8.0000,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11426020/pdf/","citationCount":"0","resultStr":"{\"title\":\"The polinton-like supergroup of viruses: evolution, molecular biology, and taxonomy.\",\"authors\":\"Eugene V Koonin, Matthias G Fischer, Jens H Kuhn, Mart Krupovic\",\"doi\":\"10.1128/mmbr.00086-23\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>SUMMARYPolintons are 15-20 kb-long self-synthesizing transposons that are widespread in eukaryotic, and in particular protist, genomes. 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引用次数: 0
摘要
摘要多核转座子是一种 15-20 kb 长的自合成转座子,广泛存在于真核生物,特别是原生生物的基因组中。除了一个转座酶和一个蛋白先导 DNA 聚合酶之外,多核苷酸还编码主要和次要果冻状卷曲荚膜蛋白、DNA 包装 ATP 酶的同源物,以及参与 Bamfordvirae 王国中多种真核病毒荚膜成熟的蛋白酶。鉴于这些结构蛋白和形态发生蛋白在多核病毒中的保守性,预测这些元素会在转座子和病毒生活方式之间交替出现,尽管迄今为止尚未检测到病毒,但这些元素被归类为前浆细胞病毒门中的病毒(Polintoviricetes 类)。与脊髓灰质炎病毒有关的还有脊椎动物腺病毒;在各种环境中发现的或整合到各种原生动物基因组中的未分类的类脊髓灰质炎病毒(Polinton-like viruses,PLVs);病毒噬菌体(Maveriviricetes),它们是包括原生动物宿主和巨型病毒在内的三方超寄生系统的一部分;以及无囊衍生物,如真菌的细胞质线性 DNA 质粒和跨病毒子。系统发生组学分析表明,波林顿类超群病毒将细菌ectivirids(前浆液病毒纲Tectiliviricetes)与包括大型和巨型真核DNA病毒在内的核细胞病毒科连接起来。通过对类脊髓灰质炎病毒编码的蛋白质进行结构比较分析,发现了以前未曾发现的功能域,如末端蛋白和与 DNA 聚合酶处理过程有关的独特蛋白酶,并澄清了脊髓灰质炎病毒门内的进化关系。在这里,我们利用这些对类似于 Polinton-like 超群的进化的洞察力,发展出一种修正的巨分类法,将 Polintoviricetes、PLVs(新类 "Aquintoviricetes")、virophages(重命名为 "Aquintoviricetes")和virophages(重命名为 "Aquintoviricetes")进行分类、Polintoviricetes)、PLVs(新类 "Aquintoviricetes")、virophages(更名为 "Virophaviricetes "类)以及腺病毒科(新类 "Pharingeaviricetes")归入前浆膜病毒亚门 "Polisuviricotina",与包括Tectiliviricetes在内的亚门("Prepoliviricotina")为姐妹亚门。
The polinton-like supergroup of viruses: evolution, molecular biology, and taxonomy.
SUMMARYPolintons are 15-20 kb-long self-synthesizing transposons that are widespread in eukaryotic, and in particular protist, genomes. Apart from a transposase and a protein-primed DNA polymerase, polintons encode homologs of major and minor jelly-roll capsid proteins, DNA-packaging ATPases, and proteases involved in capsid maturation of diverse eukaryotic viruses of kingdom Bamfordvirae. Given the conservation of these structural and morphogenetic proteins among polintons, these elements are predicted to alternate between transposon and viral lifestyles and, although virions have thus far not been detected, are classified as viruses (class Polintoviricetes) in the phylum Preplasmiviricota. Related to polintoviricetes are vertebrate adenovirids; unclassified polinton-like viruses (PLVs) identified in various environments or integrated into diverse protist genomes; virophages (Maveriviricetes), which are part of tripartite hyperparasitic systems including protist hosts and giant viruses; and capsid-less derivatives, such as cytoplasmic linear DNA plasmids of fungi and transpovirons. Phylogenomic analysis indicates that the polinton-like supergroup of viruses bridges bacterial tectivirids (preplasmiviricot class Tectiliviricetes) to the phylum Nucleocytoviricota that includes large and giant eukaryotic DNA viruses. Comparative structural analysis of proteins encoded by polinton-like viruses led to the discovery of previously undetected functional domains, such as terminal proteins and distinct proteases implicated in DNA polymerase processing, and clarified the evolutionary relationships within Polintoviricetes. Here, we leverage these insights into the evolution of the polinton-like supergroup to develop an amended megataxonomy that groups Polintoviricetes, PLVs (new class 'Aquintoviricetes'), and virophages (renamed class 'Virophaviricetes') together with Adenoviridae (new class 'Pharingeaviricetes') in a preplasmiviricot subphylum 'Polisuviricotina' sister to a subphylum including Tectiliviricetes ('Prepoliviricotina').
期刊介绍:
Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.