Koch H G, Delius H, Matz B, Flügel R M, Clarke J, Darai G
J Virol. 1985 Jul;55(1):86-95. doi: 10.1128/JVI.55.1.86-95.1985.
Purified virion DNA of about 200 kilobase pairs of tupaia herpesvirus strain 2 was cleaved with EcoRI or HindIII restriction endonuclease. Restriction fragments representing the complete viral genome including both termini were inserted into the EcoRI, HindIII, and EcoRI-HindIII sites of the bacterial plasmid pAT153. Restriction maps for the restriction endonucleases EcoRI and HindIII were constructed with data derived from Southern blot hybridizations of individual viral DNA fragments or cloned DNA fragments which were hybridized to either viral genome fragments or recombinant plasmids. The analysis revealed that the tupaia herpesvirus genome consists of a long unique sequence of 200 kilobase pairs and that inverted repeat DNA sequences of greater than 40 base pairs do not occur, in agreement with previous electron microscopic data. No DNA sequence homology was detectable between the tupaia herpesvirus DNA and the genome of murine cytomegalovirus, which was reported to have a similar structure. In addition, seven individual isolates of tupaia herpesvirus were characterized. The isolates can be grouped into five strains by their DNA cleavage patterns.
将约200千碱基对的树鼩疱疹病毒2型的纯化病毒粒子DNA用EcoRI或HindIII限制性内切酶进行切割。代表包括两个末端在内的完整病毒基因组的限制性片段被插入到细菌质粒pAT153的EcoRI、HindIII和EcoRI - HindIII位点。利用来自单个病毒DNA片段或克隆DNA片段的Southern印迹杂交数据构建了限制性内切酶EcoRI和HindIII的限制性图谱,这些片段与病毒基因组片段或重组质粒进行杂交。分析表明,树鼩疱疹病毒基因组由一个200千碱基对的长独特序列组成,并且不存在大于40个碱基对的反向重复DNA序列,这与先前的电子显微镜数据一致。在树鼩疱疹病毒DNA与据报道具有相似结构的鼠巨细胞病毒基因组之间未检测到DNA序列同源性。此外,对七个树鼩疱疹病毒的单独分离株进行了特征分析。这些分离株可根据其DNA切割模式分为五个菌株。