Owen L J, Field H J
Department of Clinical Veterinary Medicine, University of Cambridge, U.K.
Arch Virol. 1988;98(1-2):27-38. doi: 10.1007/BF01321003.
The bovine herpesvirus-1 (BHV-1) genome was analysed by Southern blot hybridization using the herpes simplex virus type 1 (HSV-1) DNA polymerase gene as a probe. A 2.5 kilobase region which hybridized specifically to the HSV-1 DNA polymerase gene was identified within the Hind III G fragment at approximate map units 0.334-0.352. In order to provide further evidence that this is the location of the BHV-1 DNA polymerase gene, the 2.5 kilobase region was cloned and part of it sequenced. An uninterrupted stretch of over 800 nucleotides was obtained and an open reading frame spanning the entire sequence was identified. The amino acid sequence that it encodes shows striking homology to a region within the C-terminal half of other herpesvirus DNA polymerases.
使用单纯疱疹病毒1型(HSV-1)DNA聚合酶基因作为探针,通过Southern印迹杂交分析了牛疱疹病毒1型(BHV-1)基因组。在Hind III G片段内,约图谱单位0.334-0.352处鉴定出一个与HSV-1 DNA聚合酶基因特异性杂交的2.5千碱基区域。为了进一步证明这是BHV-1 DNA聚合酶基因的位置,对该2.5千碱基区域进行了克隆并对其部分进行了测序。获得了一段超过800个核苷酸的不间断序列,并鉴定出一个跨越整个序列的开放阅读框。它编码的氨基酸序列与其他疱疹病毒DNA聚合酶C末端一半内的一个区域具有显著的同源性。