Parola Alejandro D, Manzán M Alejandra, Lozano Mario E, Ghiringhelli P Daniel, Sciocco-Cap Alicia, Romanowski Víctor
Institute de Bioquimica y Biología Molecular, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina.
Virus Genes. 2002 Dec;25(3):329-41. doi: 10.1023/a:1020992412175.
The bean shoot borer, Epinotia aporema (Lep. Tortricidae), is an economically important pest of legume crops in South America. Recently, a granulovirus (EpapGV) was isolated from E. aporema larvae, and evaluated as a potential biological control agent. In order to generate a restriction map and to investigate the gene organisation of EpapGV genome, DNA isolated from occlusion bodies as well as a set of cloned genomic fragments were analysed using combinations of restriction endonucleases and Southern blot analyses that lead to a first version of the physical map. It was subsequently confirmed and refined by sequencing the termini of the cloned fragments and assessing their contiguity by comparing the sequences with databases to identify putative ORFs spanning neighbour fragments. This was also aided by PCR amplifications with primers that pointed outwards of the cloned viral DNA. The granulin gene was positioned on the physical map, cloned and sequenced. Its 747-nucleotide-long ORF encodes a predicted protein of 29 kDa and the core of the baculovirus very late promoter ATAAG was found 29 nucleotides upstream the initiation codon. In addition, 27 putative ORFs were located on the map and used to explore the genome organisation by GeneParityPlot against the fully sequenced granulovirus genomes. These data, taken together with the phylogenetic tree generated by alignment of the major occlusion proteins, indicate that EpapGV is closely related to CpGV, but has a distinct gene organisation.
豆蛀螟(Epinotia aporema,鳞翅目:卷蛾科)是南美洲豆类作物的一种具有重要经济意义的害虫。最近,从豆蛀螟幼虫中分离出一种颗粒体病毒(EpapGV),并对其作为潜在生物防治剂进行了评估。为了构建限制酶图谱并研究EpapGV基因组的基因组织,使用限制性内切酶组合和Southern杂交分析对从包涵体中分离的DNA以及一组克隆的基因组片段进行了分析,从而得到了物理图谱的第一版。随后,通过对克隆片段的末端进行测序,并通过将序列与数据库进行比较以鉴定跨越相邻片段的推定开放阅读框(ORF)来评估它们的连续性,从而对该图谱进行了确认和完善。使用指向克隆病毒DNA外部的引物进行PCR扩增也有助于此过程。颗粒体蛋白基因定位在物理图谱上,进行了克隆和测序。其747个核苷酸长的开放阅读框编码一个预测的29 kDa蛋白质,并且在起始密码子上游29个核苷酸处发现了杆状病毒晚期启动子ATAAG的核心序列。此外,在图谱上定位了27个推定的开放阅读框,并通过与完全测序的颗粒体病毒基因组进行基因奇偶性图分析来探索基因组组织。这些数据,连同由主要包涵体蛋白比对产生的系统发育树,表明EpapGV与CpGV密切相关,但具有独特的基因组织。