Davison A J, Wilkie N M
J Gen Virol. 1983 Sep;64 (Pt 9):1927-42. doi: 10.1099/0022-1317-64-9-1927.
Molecular hybridization experiments were carried out to investigate homologous regions in the genomes of herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), equid herpesvirus 1 (EHV-1), pseudorabies virus (PRV) and varicella-zoster virus (VZV). Virion DNA probes from EHV-1, PRV and VZV hybridized to similar regions of the HSV genome, and the use of cloned DNA probes allowed heterologous genomes to be oriented with respect to homologous regions. The HSV-1 and HSV-2 genomes are colinear, the EHV-1 and VZV genomes are colinear with the IL or ISL genome arrangement of HSV, and the PRV genome is essentially colinear with the IL genome arrangement of HSV except that the region 0.1 to 0.4 fractional genome units appears to be inverted. A detailed analysis of sequences in the HSV-2 and PRV genomes to which the HSV-1 major capsid protein gene hybridized was carried out in order to demonstrate the application of molecular hybridization to the location of genes in heterologous genomes. The lesion in a DNA-positive temperature-sensitive mutant of PRV was mapped within the putative PRV major capsid protein gene. We conclude that the herpesviruses we have studied possess several highly conserved genes, and propose that they are similar in genetic organization despite presumably separate evolutionary histories.
进行了分子杂交实验,以研究1型和2型单纯疱疹病毒(HSV-1和HSV-2)、马疱疹病毒1型(EHV-1)、伪狂犬病病毒(PRV)和水痘-带状疱疹病毒(VZV)基因组中的同源区域。来自EHV-1、PRV和VZV的病毒体DNA探针与HSV基因组的相似区域杂交,使用克隆的DNA探针能够使异源基因组相对于同源区域进行定位。HSV-1和HSV-2基因组是共线的,EHV-1和VZV基因组与HSV的IL或ISL基因组排列共线,PRV基因组与HSV的IL基因组排列基本共线,只是在基因组0.1至0.4分数单位区域似乎是反向的。对HSV-1主要衣壳蛋白基因杂交的HSV-2和PRV基因组中的序列进行了详细分析,以证明分子杂交在异源基因组基因定位中的应用。PRV的一个DNA阳性温度敏感突变体中的损伤被定位在假定的PRV主要衣壳蛋白基因内。我们得出结论,我们所研究的疱疹病毒拥有几个高度保守的基因,并提出尽管它们可能有不同的进化历史,但它们在基因组织上是相似的。