Smith J A, Pari G S
Hybridon Inc., Worcester, Massachusetts 01605.
J Virol. 1995 Mar;69(3):1925-31. doi: 10.1128/JVI.69.3.1925-1931.1995.
It was previously reported that the region encoding human cytomegalovirus (HCMV) genes UL36 to UL38 was required for origin-dependent DNA replication. These genes encode transactivators that upregulate viral and cellular transcription. However, their requirement for viral DNA replication has not been demonstrated. We have now used an antisense phosphorothioate oligonucleotide complementary to the intron-exon boundary of the UL36 and UL37 unspliced RNA to show that these gene products are required for HCMV DNA replication. Southern analysis showed that this oligonucleotide almost completely inhibits HCMV DNA replication when used at concentrations as low as 0.08 microM. The ability of this oligonucleotide to inhibit DNA replication was not the result of an inhibition of virus adsorption. Southern blots showed no impairment of viral adsorption or internalization in the presence of either specific or nonspecific phosphorothioate oligonucleotides. In addition, Northern (RNA) blots confirm that this antisense compound specifically reduced UL36 mRNA in treated cells to undetectable levels while the steady-state levels of immediate-early transcripts IE1 and IE2 were unaffected. These results demonstrate that the UL36 and UL37 gene products provide an essential function in initiation of HCMV DNA replication.
先前有报道称,编码人巨细胞病毒(HCMV)基因UL36至UL38的区域是依赖于起始点的DNA复制所必需的。这些基因编码反式激活因子,可上调病毒和细胞转录。然而,它们对病毒DNA复制的需求尚未得到证实。我们现在使用了一种与UL36和UL37未剪接RNA的内含子-外显子边界互补的反义硫代磷酸酯寡核苷酸,以表明这些基因产物是HCMV DNA复制所必需的。Southern分析表明,当以低至0.08 microM的浓度使用时,这种寡核苷酸几乎完全抑制HCMV DNA复制。这种寡核苷酸抑制DNA复制的能力并非病毒吸附受到抑制的结果。Southern印迹显示,在存在特异性或非特异性硫代磷酸酯寡核苷酸的情况下,病毒吸附或内化均未受损。此外,Northern(RNA)印迹证实,这种反义化合物在处理过的细胞中将UL36 mRNA特异性降低至无法检测的水平,而即刻早期转录本IE1和IE2的稳态水平未受影响。这些结果表明,UL36和UL37基因产物在HCMV DNA复制起始中发挥着重要作用。