Park Chin-Ju, Bae Sung-Hun, Lee Mi-Kyung, Varani Gabriele, Choi Byong-Seok
Department of Chemistry and National Creative Research Initiative Center, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong, Yuseong-gu, Daejon 305-701, Korea.
Nucleic Acids Res. 2003 Jun 1;31(11):2824-32. doi: 10.1093/nar/gkg387.
Influenza A virus replication requires the interaction of viral RNA-dependent RNA polymerase (RdRp) with promoters in both the RNA genome (vRNA) and the full-length complementary RNA (cRNA) which serve as templates for the generation of new vRNAs. Although RdRp binds both promoters effectively, it must also discriminate between them because they serve different functional roles in the viral life cycle. Even though the inherent asymmetry between two RNA promoters is considered as a cause of the differential recognition by the RdRp, the structural basis for the ability of the RdRp to recognize the RNA promoters and discriminate effectively between them remains unsolved. Here we report the structure of the cRNA promoter of influenza A virus as determined by heteronuclear magnetic resonance spectroscopy. The terminal region is extremely unstable and does not have a rigid structure. The major groove of the internal loop is widened by the displacement of a novel A*(UU) motif toward the minor groove. These internal loop residues show distinguishable dynamic characters, with differing motional timescales for each residue. Comparison of the cRNA promoter structure with that of the vRNA promoter reveals common structural and dynamic elements in the internal loop, but also differences that provide insight into how the viral RdRp differentially recognizes the cRNA and vRNA promoters.
甲型流感病毒的复制需要病毒RNA依赖性RNA聚合酶(RdRp)与RNA基因组(vRNA)和全长互补RNA(cRNA)中的启动子相互作用,这些启动子作为生成新vRNA的模板。尽管RdRp能有效结合这两种启动子,但它也必须区分它们,因为它们在病毒生命周期中发挥着不同的功能作用。尽管两个RNA启动子之间固有的不对称性被认为是RdRp进行差异识别的原因,但RdRp识别RNA启动子并有效区分它们的结构基础仍未解决。在此,我们报告了通过异核磁共振光谱法确定的甲型流感病毒cRNA启动子的结构。其末端区域极其不稳定,没有刚性结构。内部环的大沟因一个新的A*(UU)基序向小沟的位移而变宽。这些内部环残基表现出可区分的动态特征,每个残基的运动时间尺度不同。将cRNA启动子结构与vRNA启动子结构进行比较,揭示了内部环中常见的结构和动态元件,但也存在差异,这些差异为病毒RdRp如何差异识别cRNA和vRNA启动子提供了见解。