Melchers W J, Hoenderop J G, Bruins Slot H J, Pleij C W, Pilipenko E V, Agol V I, Galama J M
Department of Medical Microbiology, University of Nijmegen, The Netherlands.
J Virol. 1997 Jan;71(1):686-96. doi: 10.1128/JVI.71.1.686-696.1997.
Higher-order RNA structures in the 3' untranslated region (3'UTR) of enteroviruses are thought to play a pivotal role in viral negative-strand RNA synthesis. The structure of the 3'UTR was predicted by thermodynamic calculations using the STAR (structural analysis of RNA) computer program and experimentally verified using chemical and enzymatic probing of in vitro-synthesized RNA. A possible pseudoknot interaction between the 3D polymerase coding sequence and domain Y and a "kissing" interaction between domains X and Y was further studied by mutational analysis, using an infectious coxsackie B3 virus cDNA clone (domain designation as proposed by E. V. Pilipenko, S. V. Maslova, A. N. Sinyakov, and V.I. Agol (Nucleic Acids Res. 20:1739-1745, 1992). The higher-order RNA structure of the 3'UTR appeared to be maintained by an intramolecular kissing interaction between the loops of the two predominant hairpin structures (X and Y) within the 3'UTR. Disturbing this interaction had no effect on viral translation and processing of the polyprotein but exerted a primary effect on viral replication, as was demonstrated in a subgenomic coxsackie B3 viral replicon, in which the capsid P1 region was replaced by the luciferase gene. Mutational analysis did not support the existence of the pseudoknot interaction between hairpin loop Y and the 3D polymerase coding sequence. Based on these experiments, we constructed a three-dimensional model of the 3'UTR of coxsackie B virus that shows the kissing interaction as the essential structural feature of the origin of replication required for its functional competence.
肠道病毒3'非翻译区(3'UTR)中的高阶RNA结构被认为在病毒负链RNA合成中起关键作用。使用STAR(RNA结构分析)计算机程序通过热力学计算预测3'UTR的结构,并通过对体外合成RNA进行化学和酶促探测进行实验验证。使用感染性柯萨奇B3病毒cDNA克隆(结构域命名由E.V. Pilipenko、S.V. Maslova、A.N. Sinyakov和V.I. Agol提出(《核酸研究》20:1739 - 1745,1992年)),通过突变分析进一步研究了3D聚合酶编码序列与结构域Y之间可能的假结相互作用以及结构域X和Y之间的“亲吻”相互作用。3'UTR的高阶RNA结构似乎由3'UTR内两个主要发夹结构(X和Y)的环之间的分子内亲吻相互作用维持。干扰这种相互作用对病毒翻译和多聚蛋白加工没有影响,但对病毒复制有主要影响,这在亚基因组柯萨奇B3病毒复制子中得到证明,其中衣壳P1区域被荧光素酶基因取代。突变分析不支持发夹环Y与3D聚合酶编码序列之间存在假结相互作用。基于这些实验,我们构建了柯萨奇B病毒3'UTR的三维模型,该模型显示亲吻相互作用是其功能活性所需复制起点的基本结构特征。