Department of Plant Biology and Forest Genetics, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Uppsala, Sweden.
J Virol. 2013 Jun;87(11):6091-103. doi: 10.1128/JVI.03322-12. Epub 2013 Mar 20.
Potato mop-top virus (PMTV) produces a defective RNA (D RNA) encompassing the 5'-terminal 479 nucleotides (nt) and 3'-terminal 372 nt of RNA-TGB (where TGB is triple gene block). The mechanism that controls D RNA biogenesis and the role of D RNA in virus accumulation was investigated by introducing deletions, insertions, and point mutations into the sequences of the open reading frames (ORFs) of TGB1 and the 8-kilodalton (8K) protein that were identified as required for efficient production of the D RNA. Transient expression of RNA-TGB in the absence of RNA-Rep (which encodes the replicase) did not result in accumulation of D RNA, indicating that its production is dependent on PMTV replication. The D RNA could be eliminated by disrupting a predicted minus-strand stem-loop structure comprising complementary sequences of the 5' TGB1 ORF and the 3' 8K ORF, suggesting intramolecular template switching during positive-strand synthesis as a mechanism for the D RNA biogenesis. Virus accumulation was reduced when the 8K ORF was disrupted but D RNA was produced. Conversely, the virus accumulated at higher titers when the 8K ORF was intact and D RNA production was blocked. These data demonstrate that the D RNA interferes with virus infection and therefore should be referred to as a defective interfering RNA (DI RNA). The 8K protein was shown to be a weak silencing suppressor. This study provides an example of the interplay between a pathogen and its molecular parasite where virus accumulation was differentially regulated by the 8K protein and DI RNA, indicating that they play antagonistic roles and suggesting a mechanism by which the virus can attenuate replication, decreasing viral load and thereby enhancing its efficiency as a parasite.
马铃薯帚顶病毒(PMTV)产生一种缺陷型 RNA(D RNA),包含 RNA-TGB 的 5'-末端 479 个核苷酸(nt)和 3'-末端 372 nt(其中 TGB 是三基因块)。通过在 TGB1 和 8 千道尔顿(8K)蛋白的开放阅读框(ORF)序列中引入缺失、插入和点突变,研究了控制 D RNA 生物发生的机制以及 D RNA 在病毒积累中的作用,这些突变被鉴定为有效产生 D RNA 所必需的。在没有 RNA-Rep(编码复制酶)的情况下瞬时表达 RNA-TGB 不会导致 D RNA 的积累,这表明其产生依赖于 PMTV 的复制。通过破坏由 5' TGB1 ORF 和 3' 8K ORF 的互补序列组成的预测负链茎环结构,可以消除 D RNA,这表明在正链合成过程中存在分子内模板转换,这是 D RNA 生物发生的一种机制。当 8K ORF 被破坏时,病毒积累减少,但 D RNA 被产生。相反,当 8K ORF 完整且 D RNA 产生被阻断时,病毒积累更高的滴度。这些数据表明 D RNA 干扰病毒感染,因此应将其称为缺陷干扰 RNA(DI RNA)。8K 蛋白是一种弱的沉默抑制子。本研究提供了一个病原体与其分子寄生虫相互作用的例子,其中 8K 蛋白和 DI RNA 对病毒积累的调节存在差异,表明它们发挥拮抗作用,并提出了一种病毒可以减弱复制、降低病毒载量从而增强其作为寄生虫效率的机制。