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甲型流感病毒重叠非结构基因中的核苷酸替换模式及其对H5N1亚型遗传多样性的影响

Pattern of nucleotide substitution in the overlapping nonstructural genes of influenza A virus and implication for the genetic diversity of the H5N1 subtype.

作者信息

Pavesi Angelo

机构信息

Department of Genetics, Biology of Microorganisms, Anthropology, Evolution, University of Parma, V. le G. P. Usberti 11/A, I-43100 Parma, Italy.

出版信息

Gene. 2007 Nov 1;402(1-2):28-34. doi: 10.1016/j.gene.2007.07.013. Epub 2007 Jul 26.

DOI:10.1016/j.gene.2007.07.013
PMID:17825505
Abstract

In viruses under strong pressure to minimize genome size, overlapping genes represent a fine strategy to condense a maximum amount of information into short nucleotide sequences. Here, we investigated the evolution of the genes encoding the nonstructural proteins NS1 and NS2 of influenza A virus (IAV), which are one of the best characterized cases of gene overlap. By a detailed analysis of about four hundred sequences grouped into 11 IAV subtypes, we found that the overlapping coding region of the NS1 gene shows a significant increase of the rate of nonsynonymous change, with respect to its nonoverlapping counterpart. The same feature was observed in the overlapping coding region of the NS2 gene. Such a variation pattern, which implies the occurrence of several amino acid substitutions in the protein regions encoded by overlapping frames, is different from the pattern of constrained evolution typical of other viral overlapping-gene systems. Amino acid sequence analysis of the NS1 and NS2 proteins revealed that some nonsynonymous substitutions, located in the region of gene overlap, play a critical role in shaping the genetic diversity of the highly pathogenic subtype H5N1. Since both proteins contribute to disease pathogenesis by affecting many virus and host-cell processes, information provided by this study should be useful to highlight the impact of nonstructural gene variation on the pathogenicity of H5N1 viruses.

摘要

在面临极大压力以最小化基因组大小的病毒中,重叠基因是一种将最大量信息压缩到短核苷酸序列中的精妙策略。在此,我们研究了甲型流感病毒(IAV)非结构蛋白NS1和NS2编码基因的进化,这是基因重叠最典型的案例之一。通过对约四百个分为11个IAV亚型的序列进行详细分析,我们发现NS1基因的重叠编码区域相对于其非重叠对应区域,非同义变化率显著增加。在NS2基因的重叠编码区域也观察到了相同特征。这种变异模式意味着在重叠阅读框编码的蛋白质区域发生了多个氨基酸替换,这与其他病毒重叠基因系统典型的受限进化模式不同。对NS1和NS2蛋白的氨基酸序列分析表明,位于基因重叠区域的一些非同义替换在塑造高致病性H5N1亚型的遗传多样性方面起着关键作用。由于这两种蛋白都通过影响许多病毒和宿主细胞过程来促进疾病发病机制,本研究提供的信息应有助于突出非结构基因变异对H5N1病毒致病性的影响。

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