Narayanan Krishna, Chen Chun-Jen, Maeda Junko, Makino Shinji
Department of Microbiology and Immunology, The University of Texas Medical Branch at Galveston, Galveston, Texas 77555-1019, USA.
J Virol. 2003 Mar;77(5):2922-7. doi: 10.1128/jvi.77.5.2922-2927.2003.
For any of the enveloped RNA viruses studied to date, recognition of a specific RNA packaging signal by the virus's nucleocapsid (N) protein is the first step described in the process of viral RNA packaging. In the murine coronavirus a selective interaction between the viral transmembrane envelope protein M and the viral ribonucleoprotein complex, composed of N protein and viral RNA containing a short cis-acting RNA element, the packaging signal, determines the selective RNA packaging into virus particles. In this report we show that expressed coronavirus envelope protein M specifically interacted with coexpressed noncoronavirus RNA transcripts containing the short viral packaging signal in the absence of coronavirus N protein. Furthermore, this M protein-packaging signal interaction led to specific packaging of the packaging signal-containing RNA transcripts into coronavirus-like particles in the absence of N protein. These findings not only highlight a novel RNA packaging mechanism for an enveloped virus, where the specific RNA packaging can occur without the core or N protein, but also point to a new, biologically important general model of precise and selective interaction between transmembrane proteins and specific RNA elements.
对于迄今为止所研究的任何一种有包膜RNA病毒而言,病毒核衣壳(N)蛋白识别特定的RNA包装信号是病毒RNA包装过程中所描述的第一步。在鼠冠状病毒中,病毒跨膜包膜蛋白M与由N蛋白和含有短顺式作用RNA元件(即包装信号)的病毒RNA组成的病毒核糖核蛋白复合体之间的选择性相互作用,决定了RNA选择性地包装进病毒颗粒中。在本报告中,我们表明,在不存在冠状病毒N蛋白的情况下,表达的冠状病毒包膜蛋白M与含有短病毒包装信号的共表达非冠状病毒RNA转录本发生特异性相互作用。此外,这种M蛋白-包装信号相互作用导致在不存在N蛋白的情况下,将含有包装信号的RNA转录本特异性包装进冠状病毒样颗粒中。这些发现不仅突出了一种有包膜病毒的新型RNA包装机制,即特定的RNA包装可以在没有核心蛋白或N蛋白的情况下发生,而且还指向了一种新的、具有生物学重要性的跨膜蛋白与特定RNA元件之间精确且选择性相互作用的一般模型。