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Structure of the Lassa virus nucleoprotein reveals a dsRNA-specific 3' to 5' exonuclease activity essential for immune suppression.拉沙病毒核蛋白结构揭示了一种 dsRNA 特异性 3' 到 5' 外切酶活性,对于免疫抑制至关重要。
Proc Natl Acad Sci U S A. 2011 Feb 8;108(6):2396-401. doi: 10.1073/pnas.1016404108. Epub 2011 Jan 24.
2
Cap binding and immune evasion revealed by Lassa nucleoprotein structure.拉沙病毒核蛋白结构揭示的帽子结合和免疫逃逸。
Nature. 2010 Dec 9;468(7325):779-83. doi: 10.1038/nature09605. Epub 2010 Nov 17.
3
Bunyaviridae RNA polymerases (L-protein) have an N-terminal, influenza-like endonuclease domain, essential for viral cap-dependent transcription.布尼亚病毒科 RNA 聚合酶(L 蛋白)具有一个 N 端的、类似流感的内切核酸酶结构域,这对于病毒的依赖帽结构的转录是必需的。
PLoS Pathog. 2010 Sep 16;6(9):e1001101. doi: 10.1371/journal.ppat.1001101.
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How RNA viruses maintain their genome integrity.RNA 病毒如何维持其基因组完整性。
J Gen Virol. 2010 Jun;91(Pt 6):1373-87. doi: 10.1099/vir.0.020818-0. Epub 2010 Mar 24.
5
The cap-snatching endonuclease of influenza virus polymerase resides in the PA subunit.流感病毒聚合酶的抢帽内切核酸酶存在于PA亚基中。
Nature. 2009 Apr 16;458(7240):914-8. doi: 10.1038/nature07745. Epub 2009 Feb 4.
6
Crystal structure of an avian influenza polymerase PA(N) reveals an endonuclease active site.禽流感聚合酶PA(N)的晶体结构揭示了一个核酸内切酶活性位点。
Nature. 2009 Apr 16;458(7240):909-13. doi: 10.1038/nature07720. Epub 2009 Feb 4.
7
Processing of genome 5' termini as a strategy of negative-strand RNA viruses to avoid RIG-I-dependent interferon induction.基因组5'末端的加工作为负链RNA病毒避免RIG-I依赖的干扰素诱导的一种策略。
PLoS One. 2008 Apr 30;3(4):e2032. doi: 10.1371/journal.pone.0002032.
8
Implications for a regulated replication of Borna disease virus in brains of experimentally infected Lewis rats.博尔纳病病毒在实验性感染的Lewis大鼠脑中的复制受调控的意义。
Virus Genes. 2008 Apr;36(2):415-20. doi: 10.1007/s11262-008-0210-8. Epub 2008 Feb 14.
9
Genome trimming by Borna disease viruses: viral replication control or escape from cellular surveillance?博尔纳病病毒的基因组修剪:病毒复制控制还是逃避细胞监测?
Cell Mol Life Sci. 2007 May;64(9):1038-42. doi: 10.1007/s00018-007-6545-9.
10
5'-Triphosphate RNA is the ligand for RIG-I.5'-三磷酸核糖核酸是维甲酸诱导基因I(RIG-I)的配体。
Science. 2006 Nov 10;314(5801):994-7. doi: 10.1126/science.1132505. Epub 2006 Oct 12.

博尔纳病病毒的基因组 RNA 在 3' 末端重排后通过内部模板模体伸长。

Genomic RNAs of Borna disease virus are elongated on internal template motifs after realignment of the 3' termini.

机构信息

Department of Virology, University of Freiburg, 79104 Freiburg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):7206-11. doi: 10.1073/pnas.1016759108. Epub 2011 Apr 11.

DOI:10.1073/pnas.1016759108
PMID:21482759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3084138/
Abstract

The terminal structures of the Borna disease virus (BDV) genome (vRNA) and antigenome (cRNA) differ from those of other negative strand RNA viruses, as both molecules possess four nucleotides at the 3' terminus without an apparent template at the 5' end of the opposite strand. Consequently, the v- and cRNA molecules are not perfect mirror images, a situation that is not compatible with conventional strategies to maintain genetic information. We show here that recombinant viruses recovered from cDNA lacking the nontemplated nucleotides efficiently reconstitute the 3' overhangs. Analyses of recombinant viruses encoding genetic markers in potential alternative template sequences demonstrated that the BDV v- and cRNA molecules are extended by a realign-and-elongation process on internal template motifs located in close proximity to the 3' ends of v- and cRNA, respectively. The data further suggest that cRNA elongation is restricted to a single template motif of the nascent strand, whereas elongation of vRNA might use multiple template motifs. We propose that the elongation of the 3' termini supports the terminal integrity of the genomic RNA molecules during BDV persistence, and furthermore provides an elegant strategy to eliminate the triphosphate groups from the 5' termini of the BDV v- and cRNA without compromising the genetic information of the virus.

摘要

博尔纳病病毒 (BDV) 基因组 (vRNA) 和抗原基因组 (cRNA) 的末端结构与其他负链 RNA 病毒不同,因为这两种分子在 3' 末端都有四个核苷酸,而在相反链的 5' 端没有明显的模板。因此,vRNA 和 cRNA 分子不是完美的镜像,这种情况与维持遗传信息的传统策略不兼容。我们在这里表明,从缺乏非模板核苷酸的 cDNA 中回收的重组病毒能够有效地重新构建 3' 突出端。对编码潜在替代模板序列中遗传标记的重组病毒的分析表明,BDV 的 vRNA 和 cRNA 分子通过重新排列和延伸过程在各自的 vRNA 和 cRNA 3' 末端附近的内部模板基序上延伸。这些数据进一步表明,cRNA 的延伸仅限于新生链的单个模板基序,而 vRNA 的延伸可能使用多个模板基序。我们提出,3' 末端的延伸在 BDV 持续存在期间支持基因组 RNA 分子的末端完整性,并且进一步提供了一种巧妙的策略,可以在不损害病毒遗传信息的情况下从 BDV vRNA 和 cRNA 的 5' 末端去除三磷酸基团。