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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.

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。

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