Suppr超能文献

流行性出血性疾病病毒(EHDV)核心蛋白VP1、VP3、VP4、VP6和VP7的遗传及系统发育分析

Genetic and phylogenetic analysis of the core proteins VP1, VP3, VP4, VP6 and VP7 of epizootic haemorrhagic disease virus (EHDV).

作者信息

Anthony S J, Maan N, Maan S, Sutton G, Attoui H, Mertens P P C

机构信息

Vector-borne Diseases Program, Institute for Animal Health, Ash Road, Pirbright, Surrey GU24 0NF, United Kingdom.

出版信息

Virus Res. 2009 Nov;145(2):187-99. doi: 10.1016/j.virusres.2009.07.011. Epub 2009 Jul 24.

Abstract

The core proteins of epizootic haemorrhagic disease virus (EHDV) have important roles to perform in maintaining the structure and function of the virus. A complete genetic and phylogenetic analysis was therefore performed on these proteins (and the genes that code for them) to allow comparison of the selective pressures acting on each. Accession numbers, gene and protein sizes, ORF positions, G+C contents, terminal hexanucleotides, start and stop codons and phylogenetic relationships are all presented. The inner core proteins (VP1, VP3, VP4 and VP6) were characterised by high levels of sequence conservation, and the ability to topotype isolates very strongly into eastern or western groups. This is particularly evident in genome segment 9 (VP6) which exists as two different sized homologues. VP7 did not topotype, but rather exhibited a more random, radial phylogeny suggestive of genetic drift. With the exception of VP6, all of the core proteins also showed high numbers of synonymous mutations in the third base position, suggesting they have been evolving for a long period of time. Interestingly, VP6 did not show this, and possible reasons for this are discussed.

摘要

流行性出血病病毒(EHDV)的核心蛋白在维持病毒的结构和功能方面发挥着重要作用。因此,对这些蛋白(以及编码它们的基因)进行了完整的遗传和系统发育分析,以便比较作用于每个蛋白的选择压力。文中呈现了登录号、基因和蛋白大小、开放阅读框位置、G+C含量、末端六核苷酸、起始和终止密码子以及系统发育关系。内核蛋白(VP1、VP3、VP4和VP6)的特点是具有高度的序列保守性,并且能够将分离株非常强烈地分为东部或西部组。这在基因组片段9(VP6)中尤为明显,该片段以两种不同大小的同源物形式存在。VP7没有进行拓扑分型,而是呈现出更随机的、放射状的系统发育,提示存在遗传漂变。除VP6外,所有核心蛋白在第三个碱基位置也显示出大量同义突变,表明它们已经进化了很长时间。有趣的是,VP6并未表现出这种情况,并对其可能的原因进行了讨论。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验