Kaerner H C, Maichle I B, Ott A, Schröder C H
Nucleic Acids Res. 1979 Apr;6(4):1467-78. doi: 10.1093/nar/6.4.1467.
During serial passages of Herpes simplex virus (HSV) at high multiplicity of infection, virions containing defective viral DNA accumulate in the progeny. The defective DNA molecules are made up by repeats of restricted portions of the standard viral genome. Two different classes of defective DNA derived from HSV-1 Angelotti (ANG) in independent series of high MOI-passages were studied. The nucleotide sequences contained in the defective DNA were localized on the parental viral genome. One of the two classes contained sequences from non-contiguous sites mapping in unique and in redundant regions of the parental DNA, whereas the second class apparently originates from the S-terminal redundant region of the parental DNA. The localization of defective DNA sequences was complicated by the fact that there exists sequence homology between the S-terminal redundancy and various unique DNA sequences in the L-segment of the HSV-1 ANG genome.
在单纯疱疹病毒(HSV)以高感染复数进行连续传代时,含有缺陷病毒DNA的病毒粒子会在子代中积累。这些缺陷DNA分子由标准病毒基因组中受限部分的重复序列组成。对独立的高感染复数传代系列中源自HSV-1安杰洛蒂株(ANG)的两类不同缺陷DNA进行了研究。缺陷DNA中包含的核苷酸序列定位在亲本病毒基因组上。这两类中的一类包含来自亲本DNA独特和冗余区域中不连续位点的序列,而另一类显然源自亲本DNA的S末端冗余区域。HSV-1 ANG基因组L片段中S末端冗余序列与各种独特DNA序列之间存在序列同源性,这一事实使得缺陷DNA序列的定位变得复杂。