Chanda P K, Chambers T M, Nayak D P
J Virol. 1983 Jan;45(1):55-61. doi: 10.1128/JVI.45.1.55-61.1983.
Influenza virus defective interfering (DI) RNAs, which originate from polymerase genes by simple internal deletion, can be transcribed in vitro. These DI RNA transcripts contain covalently linked polyadenylic acid, and their synthesis is dependent on ApG or capped RNAs as primers. Furthermore, like the standard viral RNA transcripts, they are complementary in nature and are slightly smaller in size compared with the corresponding DI RNAs. Hybridization of the specific DI RNA transcripts with the corresponding DI RNA segments and analysis of the duplex RNA by gel electrophoresis indicate that they are not incomplete polymerase gene transcripts, but rather the transcripts of the DI RNAs. Since influenza virus DI RNAs contain both the 5' and the 3' termini and transcribe polyadenylic acid-containing complementary RNAs in vitro the mechanism of interference may differ from that of the 5' DI RNAs of Sendai and vesicular stomatitis viruses.
流感病毒缺陷干扰(DI)RNA由聚合酶基因经简单内部缺失产生,可在体外转录。这些DI RNA转录本含有共价连接的聚腺苷酸,其合成依赖于ApG或加帽RNA作为引物。此外,与标准病毒RNA转录本一样,它们本质上是互补的,与相应的DI RNA相比,大小略小。特定DI RNA转录本与相应DI RNA片段的杂交以及通过凝胶电泳对双链RNA的分析表明,它们不是不完整的聚合酶基因转录本,而是DI RNA的转录本。由于流感病毒DI RNA同时包含5'和3'末端,并在体外转录含聚腺苷酸的互补RNA,因此其干扰机制可能与仙台病毒和水泡性口炎病毒的5' DI RNA不同。