Carstens E B
Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.
Virology. 1987 Nov;161(1):8-17. doi: 10.1016/0042-6822(87)90165-6.
A morphology mutant of the baculovirus Autographa californica nuclear polyhedrosis virus called M5 was previously shown to synthesize two size classes of viral DNA, one of which had a deletion of 42% of the genome. It was hypothesized that the presence of the smaller M5 circular DNA resulted from the specific deletion of the region located between two sites carrying short DNA insertions. These sites have now been identified by DNA-DNA hybridization using cloned EcoRI fragments of M5 DNA. One cloned M5 EcoRI fragment was found to correspond to the deletion junction fragment where sequences from the insertion site in the 2.6-map unit region were covalently linked to sequences from the insertion site in the 46-map unit region. The 2.6- and 46-map unit regions of Wt AcMNPV DNA were sequenced. Potential long open reading frames which would be disrupted by the M5 inserts were detected. Nucleotide sequence analysis of the same regions of M5 DNA revealed the presence of almost identical inserts of 290 bp. The primary sequence of the inserts revealed characteristics similar to the termini of transposons. Hybridization studies suggested that the inserts were derived from repetitive elements of the Spodoptera frugiperda host cell genome.
一种杆状病毒——苜蓿银纹夜蛾核型多角体病毒(Autographa californica nuclear polyhedrosis virus)的形态突变体,称为M5,此前已被证明能合成两种大小类别的病毒DNA,其中一种缺失了42%的基因组。据推测,较小的M5环状DNA的存在是由于位于携带短DNA插入片段的两个位点之间的区域发生了特异性缺失。现在已通过使用M5 DNA的克隆EcoRI片段进行DNA-DNA杂交鉴定出了这些位点。发现一个克隆的M5 EcoRI片段对应于缺失连接片段,其中来自2.6图谱单位区域插入位点的序列与来自46图谱单位区域插入位点的序列共价连接。对野生型苜蓿银纹夜蛾核型多角体病毒(Wt AcMNPV)DNA的2.6和46图谱单位区域进行了测序。检测到了可能会被M5插入片段破坏的潜在长开放阅读框。对M5 DNA相同区域的核苷酸序列分析显示存在几乎相同的290 bp插入片段。插入片段的一级序列显示出与转座子末端相似的特征。杂交研究表明,这些插入片段源自草地贪夜蛾宿主细胞基因组的重复元件。