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An in vivo cell-based assay for investigating the specific interaction between the SARS-CoV N-protein and its viral RNA packaging sequence

机译:一种基于体内细胞的分析方法用于研究SARS-CoV N蛋白与其病毒RNA包装序列之间的特异性相互作用

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摘要

The SARS-CoV nucleocapsid (N) protein serves multiple functions in viral replication, transcription, and assembly of the viral genome complex. Coronaviruses specifically package genomic RNA into assembled virions, and in SARS-CoV, it is reported that this process is driven by an interaction between the N-protein and a packaging signal encoded within the viral RNA. While recent studies have uncovered the sequence of this packaging signal, little is known about the specific interaction between the N-protein and the packaging signal sequence, and the mechanisms by which this interaction drives viral genome packaging. In this study, we developed a novel cell-based assay for examining this interaction between the N-protein and packaging signal RNA for SARS-CoV, as well as other viruses within the coronaviridae family. Our results demonstrate that the N-protein specifically recognizes the SARS-CoV packaging signal with greater affinity compared to signals from other coronaviruses or non-coronavirus species. We also use deletion mapping to identify a 151-nt region within the packaging signal sequence that is critical for N-protein-RNA binding, and conversely, we show that both the N-terminal and C-terminal domains of the N protein are necessary for recognizing the packaging RNA. These results describe, for the first time, evidence for an interaction between the SARS-CoV N-protein and its packaging signal RNA, and demonstrate the feasibility of using this cell-based assay to further probe viral RNA-protein interactions in future studies.
机译:SARS-CoV核​​衣壳(N)蛋白在病毒基因组复合体的病毒复制,转录和组装中起多种功能。冠状病毒将基因组RNA特别包装到组装的病毒体中,据报道,在SARS-CoV中,这一过程是由N蛋白与病毒RNA中编码的包装信号之间的相互作用驱动的。尽管最近的研究发现了这种包装信号的序列,但对于N蛋白与包装信​​号序列之间的特异性相互作用以及这种相互作用驱动病毒基因组包装的机制知之甚少。在这项研究中,我们开发了一种新颖的基于细胞的检测方法,用于检测SARS-CoV以及冠状病毒科家族中其他病毒的N蛋白与包装信​​号RNA之间的相互作用。我们的结果表明,与来自其他冠状病毒或非冠状病毒物种的信号相比,N蛋白以更大的亲和力特异性识别SARS-CoV包装信号。我们还使用缺失映射来确定包装信号序列中对N蛋白RNA结合至关重要的151 nt区域,相反,我们表明N蛋白的N末端和C末端结构域都是必需的用于识别包装RNA。这些结果首次描述了SARS-CoV N蛋白与其包装信号RNA之间相互作用的证据,并证明了在未来的研究中使用这种基于细胞的测定法进一步探测病毒RNA蛋白相互作用的可行性。

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