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A balance between circular and linear forms of the dengue virus genome is crucial for viral replication.

机译:登革热病毒基因组的圆形和线性形式之间的平衡对于病毒复制至关重要。

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The plasticity of viral plus strand RNA genomes is fundamental for the multiple functions of these molecules. Local and long-range RNA-RNA interactions provide the scaffold for interacting proteins of the translation, replication, and encapsidation machinery. Using dengue virus as a model, we investigated the relevance of the interplay between two alternative conformations of the viral genome during replication. Flaviviruses require long-range RNA-RNA interactions and genome cyclization for RNA synthesis. Here, we define a sequence present in the viral 3'UTR that overlaps two mutually exclusive structures. This sequence can form an extended duplex by long-range 5'-3' interactions in the circular conformation of the RNA or fold locally into a small hairpin (sHP) in the linear form of the genome. A mutational analysis of the sHP structure revealed an absolute requirement of this element for viral viability, suggesting the need of a linear conformation of the genome. Viral RNA replication showed high vulnerability to changes that alter the balance between circular and linear forms of the RNA. Mutations that shift the equilibrium toward the circular or the linear conformation of the genome spontaneously revert to sequences with different mutations that tend to restore the relative stability of the two competing structures. We propose a model in which the viral genome exists in at least two alternative conformations and the balance between these two states is critical for infectivity.
机译:病毒加链RNA基因组的可塑性对于这些分子的多种功能至关重要。局部和远程RNA-RNA相互作用为翻译,复制和衣壳化蛋白相互作用的蛋白提供了支架。使用登革热病毒作为模型,我们研究了复制过程中病毒基因组的两个替代构象之间相互作用的相关性。黄病毒需要长距离的RNA相互作用和RNA合成的基因组环化。在这里,我们定义了在病毒3'UTR中存在的与两个互斥结构重叠的序列。该序列可通过RNA的环状构型中的长距离5'-3'相互作用形成延伸的双链体,或局部折叠成基因组线性形式的小发夹(sHP)。 sHP结构的突变分析表明,该元件对病毒的生存力绝对有要求,表明需要基因组的线性构象。病毒RNA复制显示出对改变环形和线性形式的RNA之间的平衡的改变的高度脆弱性。使平衡向基因组的圆形或线性构象移动的突变自发地恢复为具有不同突变的序列,这些突变倾向于恢复两个竞争结构的相对稳定性。我们提出了一个模型,其中病毒基因组以至少两个替代构象存在,并且这两个状态之间的平衡对于感染性至关重要。

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