Patton J T, Stout E R, Bates R C
J Virol. 1979 Jun;30(3):917-22. doi: 10.1128/JVI.30.3.917-922.1979.
Transcription of the genome of the nondefective parvovirus BPV was examined in nuclei isolated from synchronized bovine fetal spleen cells. The relative levels of total RNA polymerase and RNA polymerase I, II, and III activities in nuclei isolated from BPV-infected and mock-infected cells were found to be similar throughout the course of infection. Hybridization of RNA synthesized in isolated nuceli indicated that BPV-specific RNA synthesis began during the period of 8 to 12 h postinfection and proceeded linearly until at least 20 h postinfection. By 20 h postinfection, 5% of the total RNA synthesized in nuclei from infected cells was virus specific. BPV-specific RNA synthesis was inhibited by 95% in the presence of 0.1 microgram of alpha-amanitin per ml, suggesting that the viral genome is transcribed by cellular RNA polymerase II.
在从同步化的牛胎儿脾细胞中分离出的细胞核中,对无缺陷细小病毒BPV的基因组转录进行了检测。发现在整个感染过程中,从感染BPV和模拟感染细胞中分离出的细胞核中,总RNA聚合酶以及RNA聚合酶I、II和III活性的相对水平相似。在分离出的细胞核中合成的RNA的杂交表明,BPV特异性RNA合成在感染后8至12小时开始,并呈线性进行,直至至少感染后20小时。到感染后20小时,感染细胞的细胞核中合成的总RNA的5%是病毒特异性的。在每毫升含有0.1微克α-鹅膏蕈碱的情况下,BPV特异性RNA合成被抑制了95%,这表明病毒基因组是由细胞RNA聚合酶II转录的。