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多瘤体、噬病毒体和转座病毒:病毒、转座子和免疫之间相互关联的复杂网络。

Polintons, virophages and transpovirons: a tangled web linking viruses, transposons and immunity.

机构信息

National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.

Unité Biologie Moléculaire du Gène chez les Extrêmophiles, Department of Microbiology, Institut Pasteur, Paris, France.

出版信息

Curr Opin Virol. 2017 Aug;25:7-15. doi: 10.1016/j.coviro.2017.06.008. Epub 2017 Jun 30.

Abstract

Virophages are satellite DNA viruses that depend for their replication on giant viruses of the family Mimiviridae. An evolutionary relationship exists between the virophages and Polintons, large self-synthesizing transposons that are wide spread in the genomes of diverse eukaryotes. Most of the Polintons encode homologs of major and minor icosahedral virus capsid proteins and accordingly are predicted to form virions. Additionally, metagenome analysis has led to the discovery of an expansive family of Polinton-like viruses (PLV) that are more distantly related to bona fide Polintons and virophages. Another group of giant virus parasites includes small, linear, double-stranded DNA elements called transpovirons. Recent in-depth comparative genomic analysis has yielded evidence of the origin of the PLV and the transpovirons from Polintons. Integration of virophage genomes into genomes of both giant viruses and protists has been demonstrated. Furthermore, in an experimental coinfection system that consisted of a protist host, a giant virus and an associated virophage, the virophage integrated into the host genome and, after activation of its expression by a superinfecting giant virus, served as an agent of adaptive immunity. There is a striking analogy between this mechanism and the CRISPR-Cas system of prokaryotic adaptive immunity. Taken together, these findings show that Polintons, PLV, virophages and transpovirons form a dynamic network of integrating mobile genetic elements that contribute to the cellular antivirus defense and host-virus coevolution.

摘要

类病毒是依赖巨型病毒家族 mimiviridae 进行复制的卫星 DNA 病毒。类病毒与 Polintons 之间存在进化关系,Polintons 是广泛存在于多种真核生物基因组中的大型自我合成转座子。大多数 Polintons 编码主要和次要二十面体病毒衣壳蛋白的同源物,因此预计会形成病毒粒子。此外,宏基因组分析导致发现了一个广泛的 Polinton 样病毒 (PLV) 家族,它们与真正的 Polintons 和类病毒的关系更远。另一组巨型病毒寄生虫包括称为转座病毒的小型线性双链 DNA 元件。最近深入的比较基因组分析为 PLV 和转座病毒的起源提供了证据,这些起源于 Polintons。已经证明类病毒基因组整合到巨型病毒和原生生物的基因组中。此外,在一个由原生生物宿主、巨型病毒和相关类病毒组成的实验混合感染系统中,类病毒整合到宿主基因组中,并且在被超感染的巨型病毒激活其表达后,作为适应性免疫的代理。这种机制与原核适应性免疫的 CRISPR-Cas 系统之间存在惊人的相似性。综上所述,这些发现表明 Polintons、PLV、类病毒和转座病毒形成了一个整合移动遗传元件的动态网络,这些元件有助于细胞抗病毒防御和宿主-病毒共同进化。

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