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Direct repeats in the 3' untranslated regions of mosquito-borne flaviviruses: possible implications for virus transmission

机译:在蚊子传播的黄病毒的3'非翻译区域中直接重复:可能对病毒传播的影响

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摘要

Direct repeats (DRs) of 20–45 nucleotide conserved sequences (CS) and repeated CS (RCS), separated by non-conserved sequences up to 100 nucleotides long, were previously described in the 3' untranslated region (3'UTR) of the three major mosquito-borne flavivirus (MBFV) subgroups, represented by Japanese encephalitis virus, Yellow fever virus and Dengue virus. Each subgroup exhibits a specific pattern of DRs, the biological significance of which has not yet been adequately addressed. The DRs were originally identified using conventional alignment programs based on the assumption that genetic variation is driven primarily by nucleotide substitutions. Since there are no recognized alignment programs that can adequately accommodate very divergent sequences, a method has been devised to construct and analyse a substantially improved 3'UTR alignment between these highly divergent viruses, based on the concept that deletions and/or insertions, in addition to substitutions, are important drivers of 3'UTR evolution. This ‘robust alignment’ approach demonstrated more extensive homologies in the 3'UTR than had been recognized previously and revealed the presence of similar DRs, either intact or as sequence ‘remnants’, in all the MBFV subgroups. The relevance of these observations is discussed in relation to (i) the function of DRs as elements of replication enhancement, (ii) the evolution of RNA secondary structures and (iii) the significance of DRs and secondary structures in MBFV transmissibility between vertebrate and invertebrate hosts. \ud
机译:先前在20-45个核苷酸的保守序列(CS)和重复CS(RCS)之间的直接重复(DR)由长达100个核苷酸的非保守序列隔开,之前在其3'非翻译区(3'UTR)中进行了描述日本脑炎病毒,黄热病病毒和登革热病毒代表三个主要的蚊媒黄病毒(MBFV)亚组。每个亚组都表现出特定的DR模式,其生物学意义尚未得到充分解决。 DRs最初是使用常规比对程序来确定的,其前提是遗传变异主要由核苷酸取代驱动。由于没有公认的比对程序可以充分适应非常不同的序列,因此,基于缺失和/或插入的概念,已设计出一种方法来构建和分析这些高度不同的病毒之间显着改善的3'UTR比对。替代是3'UTR进化的重要驱动力。这种“稳健的比对”方法在3'UTR中展示了比以前更广泛的同源性,并揭示了在所有MBFV亚组中存在完整的DR序列或类似的DR残基。这些观察的相关性与(i)DRs作为复制增强元件的功能,(ii)RNA二级结构的进化以及(iii)DRs和二级结构在脊椎动物和无脊椎动物之间MBFV传递性中的重要性相关地进行了讨论。主机。 \ ud

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