Wirth U V, Gunkel K, Engels M, Schwyzer M
Institut für Virologie der Universität Zürich, Switzerland.
J Virol. 1989 Nov;63(11):4882-9. doi: 10.1128/JVI.63.11.4882-4889.1989.
Northern (RNA) blot analysis was used to determine the spatial and temporal distribution of bovine herpesvirus 1 (BHV-1) transcripts. Total RNA was isolated from Madin-Darby bovine kidney cells which had been infected with BHV-1.2b strain K22 or BHV-1.1 strain Jura in the presence or absence of metabolic inhibitors. Cloned restriction fragments representing the entire genome of strain K22 were labeled with 32P and hybridized to immobilized RNA. A total of 54 BHV-1 transcripts were found, ranging in size from 0.4 to larger than 8 kilobases (kb). The inverted repeat regions and an adjacent segment of the unique large part of the BHV-1 genome encoded three major immediate-early (IE) transcripts and one minor IE transcript enriched after cycloheximide treatment of infected cells. Late transcripts were identified by drastically reduced abundance after cytosine arabinoside (araC) treatment. Twelve late transcripts were encoded mainly by the unique long genome region, with a cluster of four transcripts located on HindIII fragment K (map units 0.677 to 0.733). The 21 transcripts unaffected by araC treatment were defined as early; they showed dispersed locations over the whole genome, with a cluster on the unique short sequence. The 17 remaining transcripts could not be classified unambiguously as early or late by these techniques. The IE transcript with a size of 4.2 kb exhibited homology with the single IE gene of pseudorabies virus, and the IE transcript with a size of 2.9 kb was encoded in part by the genome region known to be transcriptionally active during latency.
采用Northern(RNA)印迹分析来确定牛疱疹病毒1型(BHV-1)转录本的时空分布。从感染了BHV-1.2b株K22或BHV-1.1株尤拉的Madin-Darby牛肾细胞中分离总RNA,细胞培养时存在或不存在代谢抑制剂。用32P标记代表K22株全基因组的克隆限制性片段,并与固定化的RNA杂交。共发现54种BHV-1转录本,大小从0.4千碱基(kb)到大于8千碱基不等。BHV-1基因组独特大片段的反向重复区域和相邻片段编码三种主要的立即早期(IE)转录本和一种在感染细胞经环己酰亚胺处理后富集的次要IE转录本。通过胞嘧啶阿拉伯糖苷(araC)处理后丰度大幅降低来鉴定晚期转录本。12种晚期转录本主要由独特的长基因组区域编码,其中一组四个转录本位于HindIII片段K上(图谱单位0.677至0.733)。21种不受araC处理影响的转录本被定义为早期转录本;它们在整个基因组中分布分散,在独特的短序列上有一个簇。通过这些技术,其余17种转录本无法明确归类为早期或晚期。大小为4.2 kb的IE转录本与伪狂犬病病毒的单个IE基因具有同源性,大小为2.9 kb的IE转录本部分由已知在潜伏期间具有转录活性的基因组区域编码。