Heilbronn R, Bürkle A, Stephan S, zur Hausen H
Deutsches Krebsforschungszentrum, Heidelberg, Federal Republic of Germany.
J Virol. 1990 Jun;64(6):3012-8. doi: 10.1128/JVI.64.6.3012-3018.1990.
Herpes simplex virus (HSV) induces within the host cell genome DNA amplification which can be suppressed by coinfection with adeno-associated virus (AAV). To characterize the AAV functions mediating this effect, cloned AAV type 2 wild-type or mutant genomes were transfected into simian virus 40 (SV40)-transformed hamster cells together with the six HSV replication genes (encoding UL5, UL8, major DNA-binding protein, DNA polymerase, UL42, and UL52) which together are necessary and sufficient for the induction of SV40 DNA amplification (R. Heilbronn and H. zur Hausen, J. Virol. 63:3683-3692, 1989). The AAV rep gene was identified as being responsible for the complete inhibition of HSV-induced SV40 DNA amplification. Likewise, rep inhibited origin-dependent HSV replication. rep neither killed the transfected host cells nor interfered with gene expression from the cotransfected amplification genes. This points to a specific interference with HSV-induced DNA amplification.
单纯疱疹病毒(HSV)可在宿主细胞基因组内诱导DNA扩增,而腺相关病毒(AAV)的共感染可抑制这种扩增。为了鉴定介导这种效应的AAV功能,将克隆的2型AAV野生型或突变型基因组与六个HSV复制基因(编码UL5、UL8、主要DNA结合蛋白、DNA聚合酶、UL42和UL52)一起转染到猴病毒40(SV40)转化的仓鼠细胞中,这六个基因共同对诱导SV40 DNA扩增是必需且充分的(R. Heilbronn和H. zur Hausen,《病毒学杂志》63:3683 - 3692,1989年)。AAV rep基因被确定为对HSV诱导的SV40 DNA扩增的完全抑制负责。同样,rep抑制依赖于起始位点的HSV复制。rep既不杀死转染的宿主细胞,也不干扰共转染的扩增基因的表达。这表明其对HSV诱导的DNA扩增存在特异性干扰。