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Molecular evolution of the gamma-Herpesvirinae

机译:γ-疱疹病毒的分子进化

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摘要

Genomic sequences available for members of the gamma -Herpesvirinae allow analysis of man) aspects of the group's evolution. This paper examines four topics: (i) the phylogen of the group; (ii) tile histories of gamma -herpesvirus-specific genes; (iii) genomic variation of human herpesvirus 8 (HHV-8); and (iv) the relationship between Epstein-Barr virus types 1 and 2 (EBV-1 and EBV-2). A phylogenetic tree based on eight conserved genes has been constructed for eight gamma -herpesviruses and extended to 14 species with smaller gene sets. This gave a generally robust assignment of evolutionary relationships, with tile exception of murine herpesvirus 4 (MHV-4), which could not be placed unambiguously on the tree and which has evidently experienced an unusually high rate of genomic change. The gamma -herpesviruses possess a variable complement of genes with cellular homologues. In the clearest cases these virus genes were shown to have originated from host genome lineages in the distant past. HHV-8 possesses at its left genomic terminus a highly diverse gene (KI) and at its right terminus;l gene (K15) having two diverged alleles. It was proposed that the high diversity of XI results from a positive selection on K1 and a hitchhiking effect that reduces diversity elsewhere in the genome. EBV-1 and EBV-2 differ in their alleles of the EBNA-2, EBNA-3A, EBNA-3B and EBNA-3C genes. It was suggested that EBV-1 and EBV-2 may recombine in mixed infections so that their sequence:; outside these genes remain homogeneous. Models for genesis of the types, by recombination between diverged parents or by local divergence from a single lineage, both present difficulties. [References: 75]
机译:可用于γ-疱疹病毒的成员的基因组序列允许分析该群体进化的人方面。本文研究了四个主题:(i)群体的系统发育; (ii)伽玛疱疹病毒特异性基因的历史; (iii)人疱疹病毒8(HHV-8)的基因组变异; (iv)1型和2型爱泼斯坦-巴尔病毒(EBV-1和EBV-2)之间的关系。基于八种保守基因的系统树已经为八种γ-疱疹病毒构建,并扩展到具有较小基因集的14种。除了鼠疱疹病毒4(MHV-4)例外,这给进化关系提供了一个总体上稳固的分配,这种病毒不能明确地放在树上,并且显然经历了异常高的基因组变化率。 γ-疱疹病毒具有与细胞同源物的可变的基因补体。在最明显的情况下,这些病毒基因被证明起源于遥远的过去的宿主基因组谱系。 HHV-8在其左基因组末端具有高度多样性的基因(KI),在其右末端具有1个具有两个不同等位基因的基因(K15)。有人提出,XI的高度多样性是由对K1的正选择和搭便车效应导致的,该搭便车效应降低了基因组其他地方的多样性。 EBV-1和EBV-2在EBNA-2,EBNA-3A,EBNA-3B和EBNA-3C基因的等位基因上有所不同。有人建议EBV-1和EBV-2可能在混合感染中重组,因此其顺序为:这些基因之外保持同源。通过不同父母之间的重组或单一血统的局部差异来建立这种类型的起源的模型都存在困难。 [参考:75]

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