Volkening Jeremy D, Spatz Stephen J
BASE2BIO, Madison, WI 53714, USA.
Avian Dis. 2013 Jun;57(2 Suppl):401-8. doi: 10.1637/10410-100312-Reg.1.
Herpesvirus replication within host cells results in concatemeric genomic DNA, which is cleaved into unit-length genomes and packaged into the capsid by a complex of proteins. The sites of cleavage have been identified for many herpesviruses, and conserved signaling sequences involved in cleavage and packaging have been characterized. The cleavage/packaging motifs pac-1, pac-2, and DR1 and two distinct groups of telomeric repeat sequences (static TRS and variable TRS) have been identified. By sequencing the termini of the gallid herpesvirus type 2 (GaHV-2) strain CU-2, two different cleavage sites (classical and aberrant) have been identified. Unlike classical cleavage of human herpesvirus type 1, which occurs within the DR1 site, classical cleavage of the GaHV-2 concatemers occurs 8.5 bp upstream of the DR1 site and results in an S-terminus containing telomeric repeats. Aberrant cleavage occurs the same distance from the DR1 site and generates a telomeric S-terminus but an L-terminus lacking an a sequence. These results are consistent with previous findings in other herpesviruses and should prove useful in the future study and manipulation of the GaHV-2 genome.
疱疹病毒在宿主细胞内复制会产生串联体基因组DNA,该DNA被切割成单位长度的基因组,并通过一组蛋白质包装进衣壳。许多疱疹病毒的切割位点已被确定,参与切割和包装的保守信号序列也已得到表征。已鉴定出切割/包装基序pac-1、pac-2和DR1以及两组不同的端粒重复序列(静态TRS和可变TRS)。通过对鸡疱疹病毒2型(GaHV-2)毒株CU-2的末端进行测序,已确定了两个不同的切割位点(经典位点和异常位点)。与1型人疱疹病毒在DR1位点内发生的经典切割不同,GaHV-2串联体的经典切割发生在DR1位点上游8.5 bp处,并产生一个包含端粒重复序列的S末端。异常切割发生在距DR1位点相同距离处,并产生一个端粒S末端,但L末端缺少α序列。这些结果与之前在其他疱疹病毒中的发现一致,并且在未来对GaHV-2基因组的研究和操作中应会证明是有用的。