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通过恢复沃森-克里克碱基对打破脊髓灰质炎病毒3'-UTR Y-茎中的伪二重对称。

Breaking pseudo-twofold symmetry in the poliovirus 3'-UTR Y-stem by restoring Watson-Crick base pairs.

作者信息

Zoll Jan, Tessari Marco, Van Kuppeveld Frank J M, Melchers Willem J G, Heus Hans A

机构信息

Institute for Molecules and Materials, Laboratory of Biophysical Chemistry, Radboud University Nijmegen, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands.

出版信息

RNA. 2007 May;13(5):781-92. doi: 10.1261/rna.375607.

Abstract

The previously described NMR structure of a 5'-CU-3'/5'-UU-3' motif, which is highly conserved within the 3'-UTR Y-stem of poliovirus-like enteroviruses, revealed striking regularities of the local helix geometry, thus retaining the pseudo-twofold symmetry of the RNA helix. A mutant virus with both pyrimidine base pairs changed into Watson-Crick replicated as wild type, indicating the functional importance of this symmetry relation in viral RNA replication. Here we investigated the effect of changing only one of the two pyrimidine base pairs to Watson-Crick. We determined the NMR structures of two Y-stem variants: one containing the 5'-CU-3'/5'-AU-3' motif, which has been found in wild-type virus isolates as well, and the other containing a 5'-CU-3'/5'-UG-3' motif, which is not present in any enterovirus sequenced to date. Both structures show single pyrimidine mismatches with intercalated bases. In the 5'-CU-3'/5'-AU-3' motif a C-U Watson-Crick-type base pair is formed that retains the pseudo-twofold symmetry, while in the 5'-CU-3'/5'-UG-3' motif a single asymmetric U-U mismatch breaks the twofold symmetry. Surprisingly, for the nonnatural variant no effect of the single base-pair replacement was observed on polioviral RNA replication using an in vitro replicon assay.

摘要

先前描述的5'-CU-3'/5'-UU-3'基序的核磁共振结构在脊髓灰质炎病毒样肠道病毒的3'-UTR Y-茎内高度保守,揭示了局部螺旋几何结构的显著规律,从而保留了RNA螺旋的伪二重对称性。一种将两个嘧啶碱基对都变为沃森-克里克碱基对的突变病毒能像野生型一样复制,这表明这种对称关系在病毒RNA复制中具有功能重要性。在此,我们研究了仅将两个嘧啶碱基对中的一个变为沃森-克里克碱基对的影响。我们确定了两种Y-茎变体的核磁共振结构:一种含有5'-CU-3'/5'-AU-3'基序,该基序也在野生型病毒分离株中发现;另一种含有5'-CU-3'/5'-UG-3'基序,该基序在迄今为止测序的任何肠道病毒中都不存在。两种结构都显示出带有插入碱基的单个嘧啶错配。在5'-CU-3'/5'-AU-3'基序中形成了一个C-U沃森-克里克型碱基对,保留了伪二重对称性,而在5'-CU-3'/5'-UG-3'基序中,单个不对称的U-U错配打破了二重对称性。令人惊讶的是,对于这种非天然变体,使用体外复制子测定法未观察到单碱基对替换对脊髓灰质炎病毒RNA复制有影响。

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