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呼肠孤病毒S2基因内的序列多样性:呼肠孤病毒基因在自然界中发生重配,并且预测其末端会形成一个柄环基序。

Sequence diversity within the reovirus S2 gene: reovirus genes reassort in nature, and their termini are predicted to form a panhandle motif.

作者信息

Chapell J D, Goral M I, Rodgers S E, dePamphilis C W, Dermody T S

机构信息

Department of Microbiology & Immunology, Vanderbilt Medical School, Nashville, Tennessee 37232-2581.

出版信息

J Virol. 1994 Feb;68(2):750-6. doi: 10.1128/JVI.68.2.750-756.1994.

Abstract

To better understand genetic diversity within mammalian reoviruses, we determined S2 nucleotide and deduced sigma 2 amino acid sequences of nine reovirus strains and compared these sequences with those of prototype strains of the three reovirus serotypes. The S2 gene and sigma 2 protein are highly conserved among the four type 1, one type 2, and seven type 3 strains studied. Phylogenetic analyses based on S2 nucleotide sequences of the 12 reovirus strains indicate that diversity within the S2 gene is independent of viral serotype. Additionally, we found marked topological differences between phylogenetic trees generated from S1 and S2 gene nucleotide sequences of the seven type 3 strains. These results demonstrate that reovirus S1 and S2 genes have distinct evolutionary histories, thus providing phylogenetic evidence for lateral transfer of reovirus genes in nature. When variability among the 12 sigma 2-encoding S2 nucleotide sequences was analyzed at synonymous positions, we found that approximately 60 nucleotides at the 5' terminus and 30 nucleotides at the 3' terminus were markedly conserved in comparison with other sigma 2-encoding regions of S2. Predictions of RNA secondary structures indicate that the more conserved S2 sequences participate in the formation of an extended region of duplex RNA interrupted by a pair of stem-loops. Among the 12 deduced sigma 2 amino acid sequences examined, substitutions were observed at only 11% of amino acid positions. This finding suggests that constraints on the structure or function of sigma 2, perhaps in part because of its location in the virion core, have limited sequence diversity within this protein.

摘要

为了更好地理解哺乳动物呼肠孤病毒的遗传多样性,我们测定了9株呼肠孤病毒的S2核苷酸序列并推导了σ2氨基酸序列,还将这些序列与三种呼肠孤病毒血清型的原型毒株序列进行了比较。在所研究的4株1型、1株2型和7株3型毒株中,S2基因和σ2蛋白高度保守。基于12株呼肠孤病毒S2核苷酸序列的系统发育分析表明,S2基因内的多样性与病毒血清型无关。此外,我们发现由7株3型毒株的S1和S2基因核苷酸序列生成的系统发育树之间存在明显的拓扑差异。这些结果表明,呼肠孤病毒S1和S2基因具有不同的进化历史,从而为呼肠孤病毒基因在自然界中的横向转移提供了系统发育证据。当分析12个编码σ2的S2核苷酸序列在同义位点的变异性时,我们发现与S2的其他编码σ2区域相比,5'端约60个核苷酸和3'端约30个核苷酸明显保守。RNA二级结构预测表明,更保守的S2序列参与了由一对茎环中断的双链RNA延伸区域的形成。在所检测的12个推导σ2氨基酸序列中,仅在11%的氨基酸位置观察到替换。这一发现表明,对σ2结构或功能的限制,可能部分是由于其在病毒粒子核心中的位置,限制了该蛋白内的序列多样性。

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