Heldens J G, Liu Y, Zuidema D, Goldbach R W, Vlak J M
Department of Virology, Wageningen Agricultural University, The Netherlands.
Virus Res. 1998 Jun;55(2):187-98. doi: 10.1016/s0168-1702(98)00040-9.
A DNA fragment of 11.3 kilobase pairs (kbp) in size of the baculovirus Spodoptera exigua multicapsid nucleopolyhedrovirus (SeMNPV) genome (46.5 to 55.1 m.u.) was completely sequenced. Analysis of the sequence revealed eleven potential open reading frames (ORF). Ten of these ORFs showed significant amino acid identity to Autographa californica MNPV (AcMNPV) and Orgyia pseudotsugata MNPV (OpMNPV) genes p6.9, lef5, 38K, p19, p143, p25, p18, vp33, lef4, and vp39. One ORF (XC12) has no homolog in other baculoviruses and may be unique to SeMNPV. All but three of these putative genes are preceded by the consensus baculovirus late promoter element (5'-ATAAG-3'). The genetic organization and the putative map of transcripts of this fragment suggested that this region is highly similar to a region in AcMNPV fragment EcoRI-D. Comparison of the genetic organization of this 11.3 kbp fragment with the genomes of AcMNPV, OpMNPV, Bombyx mori NPV (BmNPV) and SeMNPV revealed that this region is highly conserved among baculovirus genomes. This is in contrast to the genetic organization of the polyhedrin-p10 region, which is much more diverged, but has been taken as point of reference to orient baculovirus physical maps. Through its diversity the latter region, however, would be an excellent candidate to determine baculovirus relatedness and phylogeny. The presence of conserved and diverged regions in baculovirus genomes with respect to gene order is reminiscent to the situation in other large DNA viruses, such as herpes- and poxviruses, where conserved central and diverged terminal parts are common characteristics. The role of this feature in the genomic organization of large DNA viruses is discussed with particular emphasis on virus replication and evolution.
对杆状病毒甜菜夜蛾多粒包埋核型多角体病毒(SeMNPV)基因组中一段大小为11.3千碱基对(kbp)(46.5至55.1个图距单位)的DNA片段进行了全序列测定。序列分析揭示了11个潜在的开放阅读框(ORF)。其中10个ORF与苜蓿银纹夜蛾核型多角体病毒(AcMNPV)和黄杉毒蛾核型多角体病毒(OpMNPV)的基因p6.9、lef5、38K、p19、p143、p25、p18、vp33、lef4和vp39具有显著的氨基酸同一性。一个ORF(XC12)在其他杆状病毒中没有同源物,可能是SeMNPV所特有的。除三个推定基因外,所有这些推定基因之前都有杆状病毒晚期启动子共有元件(5'-ATAAG-3')。该片段的遗传组织和推定转录图谱表明,该区域与AcMNPV片段EcoRI-D中的一个区域高度相似。将这个11.3 kbp片段的遗传组织与AcMNPV、OpMNPV、家蚕核型多角体病毒(BmNPV)和SeMNPV的基因组进行比较,发现该区域在杆状病毒基因组中高度保守。这与多角体蛋白-p10区域的遗传组织形成对比,后者差异大得多,但已被用作确定杆状病毒物理图谱的参考点。然而,通过其多样性,后一个区域将是确定杆状病毒亲缘关系和系统发育的极佳候选区域。杆状病毒基因组中关于基因顺序的保守和差异区域的存在让人联想到其他大型DNA病毒,如疱疹病毒和痘病毒的情况,在这些病毒中,保守的中央部分和差异的末端部分是共同特征。特别强调病毒复制和进化,讨论了这一特征在大型DNA病毒基因组组织中的作用。