Ozawa K, Ayub J, Young N
Cell Biology Section, National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892.
J Virol. 1988 Jul;62(7):2508-11. doi: 10.1128/JVI.62.7.2508-2511.1988.
We have analyzed the coding capacity of B19 parvovirus transcripts by in vitro translation using the negative hybrid selection technique. Five different antisense oligonucleotides (18-mers) corresponding to different portions of the B19 genome were hybridized to RNA samples extracted from human erythroid bone marrow cells infected with B19 parvovirus in vitro, and RNase H was added to cleave specific B19 RNA molecules at selected sites. B19-specific translation products of these RNA samples were determined by immunoprecipitation. We localized the B19 nonstructural protein to the left-side transcript and the two capsid proteins to overlapping transcripts from the right side of the genome.
我们使用负向杂交筛选技术通过体外翻译分析了B19细小病毒转录本的编码能力。将与B19基因组不同部分对应的五种不同反义寡核苷酸(18聚体)与体外感染B19细小病毒的人红系骨髓细胞提取的RNA样本杂交,并添加核糖核酸酶H在选定位点切割特定的B19 RNA分子。通过免疫沉淀确定这些RNA样本的B19特异性翻译产物。我们将B19非结构蛋白定位到左侧转录本,将两种衣壳蛋白定位到基因组右侧的重叠转录本。