Jacobson S J, Konings D A, Sarnow P
Department of Biochemistry, Biophysics and Genetics, University of Colorado Health Sciences Center, Denver 80262.
J Virol. 1993 Jun;67(6):2961-71. doi: 10.1128/JVI.67.6.2961-2971.1993.
The sequences in the plus-stranded poliovirus RNA genome that dictate the specific amplification of viral RNA in infected cells remain unknown. We have analyzed the structure of the 3' noncoding region of the viral genome by thermodynamic-based structure calculation and by chemical and enzymatic probing of in vitro-synthesized RNAs and provide evidence for the existence of an RNA pseudoknot structure in this region. To explore the functional significance of this structure, revertants of a mutant bearing a lesion in the proposed pseudoknot and exhibiting a temperature-sensitive defect in viral RNA synthesis were isolated and mapped. The results of this genetic analysis established a correlation between the structure of the 3' terminus of the viral RNA and its function in vivo in RNA amplification. Furthermore, phylogenetic analysis indicated that a similar structure could be formed in coxsackievirus B1, a related enterovirus, which further supports a role for the pseudoknot structure in viral RNA amplification in infected cells.
在感染细胞中决定病毒RNA特异性扩增的正链脊髓灰质炎病毒RNA基因组序列仍然未知。我们通过基于热力学的结构计算以及对体外合成RNA的化学和酶促探测,分析了病毒基因组3'非编码区的结构,并提供证据表明该区域存在RNA假结结构。为了探究该结构的功能意义,分离并定位了一个在拟假结处有损伤且在病毒RNA合成中表现出温度敏感缺陷的突变体的回复突变体。该遗传分析结果确立了病毒RNA 3'末端结构与其在体内RNA扩增功能之间的相关性。此外,系统发育分析表明,在相关肠道病毒柯萨奇病毒B1中也可形成类似结构,这进一步支持了假结结构在感染细胞中病毒RNA扩增中的作用。