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Replication of murine coronavirus defective interfering RNA from negative-strand transcripts.

机译:从负链转录本中复制鼠冠状病毒缺陷干扰RNA。

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摘要

The positive-strand defective interfering (DI) RNA of the murine coronavirus mouse hepatitis virus (MHV), when introduced into MHV-infected cells, results in DI RNA replication and accumulation. We studied whether the introduction of negative-strand transcripts of MHV DI RNA would also result in replication. At a location downstream of the T7 promoter and upstream of the human hepatitis delta virus ribozyme domain, we inserted a complete cDNA clone of MHV DI RNA in reverse orientation; in vitro-synthesized RNA from this plasmid yielded a negative-strand RNA copy of the MHV DI RNA. When the negative-strand transcripts of the DI RNA were expressed in MHV-infected cells by a vaccinia virus T7 expression system, positive-strand DI RNAs accumulated in the plasmid-transfected cells. DI RNA replication depended on the expression of T7 polymerase and on the presence of the T7 promoter. Transfection of in vitro-synthesized negative-strand transcripts into MHV-infected cells and serial passage of virus samples from RNA-transfected cells also resulted in accumulation of the DI RNA. Positive-strand DI RNA transcripts were undetectable in sample preparations of the in vitro-synthesized negative-strand DI RNA transcripts, and DI RNA did not accumulate after cotransfection of a small amount of positive-strand DI RNA and truncated-replication-disabled negative-strand transcripts; clearly, the DI RNA replicated from the transfected negative-strand transcripts and not from minute amounts of positive-strand DI RNAs that might be envisioned as artifacts of T7 transcription. Sequence analysis of positive-strand DI RNAs in the cells transfected with negative-strand transcripts showed that DI RNAs maintained the DI-specific unique sequences introduced within the leader sequence. These data indicated that positive-strand DI RNA synthesis occurred from introduced negative-strand transcripts in the MHV-infected cells; this demonstration, using MHV, of DI RNA replication from transfected negative-strand DI RNA transcripts is the first such demonstration among all positive-stranded RNA viruses.
机译:将鼠冠状病毒小鼠肝炎病毒(MHV)的正链缺陷干扰(DI)RNA引入MHV感染的细胞后,会导致DI RNA复制和积累。我们研究了MHV DI RNA负链转录物的引入是否也会导致复制。在T7启动子下游和人肝炎三角洲病毒核酶结构域上游的位置,我们以反向插入了MHV DI RNA的完整cDNA克隆。从该质粒体外合成的RNA产生了MHV DI RNA的负链RNA拷贝。当通过牛痘病毒T7表达系统在MHV感染的细胞中表达DI RNA的负链转录物时,在质粒转染的细胞中积累了正链DI RNA。 DI RNA复制取决于T7聚合酶的表达和T7启动子的存在。体外合成的负链转录物转染到MHV感染的细胞中,以及RNA感染的细胞中病毒样品的连续传代也导致DI RNA的积累。在体外合成的负链DI RNA转录本的样品制备中无法检测到正链DI RNA转录本,并且在共转染少量正链DI RNA和截短-复制-禁用的负-后,DI RNA不会积累。转录本;显然,DI RNA是从转染的负链转录本复制而来的,而不是从可能被设想为T7转录伪像的少量正链DI RNA复制的。用负链转录本转染的细胞中正链DI RNA的序列分析表明,DI RNA保持了导入前导序列中的DI特异性独特序列。这些数据表明正链DI RNA的合成是由MHV感染细胞中引入的负链转录本产生的。使用MHV进行的从转染的负链DI RNA转录本复制DI RNA的演示是所有正链RNA病毒中的第一个此类演示。

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