Gritsun T S, Gould E A
Centre for Ecology and Hydrology, Mansfield Road, Oxford OX1 3SR, UK.
J Gen Virol. 2006 Nov;87(Pt 11):3297-3305. doi: 10.1099/vir.0.82235-0.
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.
先前在以日本脑炎病毒、黄热病病毒和登革热病毒为代表的三个主要蚊媒黄病毒(MBFV)亚组的3'非翻译区(3'UTR)中描述了由20 - 45个核苷酸保守序列(CS)和重复CS(RCS)组成的直接重复序列(DR),这些重复序列被长达100个核苷酸的非保守序列隔开。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探讨。DR最初是使用基于遗传变异主要由核苷酸替换驱动这一假设的传统比对程序鉴定出来的。由于没有公认的能充分适应差异极大序列的比对程序,因此设计了一种方法,基于除替换外,缺失和/或插入也是3'UTR进化重要驱动因素这一概念,构建并分析这些高度分化病毒之间大幅改进的3'UTR比对。这种“稳健比对”方法显示3'UTR中的同源性比之前认识到的更广泛,并揭示了所有MBFV亚组中都存在相似的DR,要么完整存在,要么作为序列“残余”存在。本文结合以下几点讨论了这些观察结果的相关性:(i)DR作为复制增强元件的功能;(ii)RNA二级结构的进化;(iii)DR和二级结构在MBFV在脊椎动物和无脊椎动物宿主之间传播中的意义。