Zhang C X, Decaussin G, de Turenne Tessier M, Daillie J, Ooka T
Nucleic Acids Res. 1987 Mar 25;15(6):2707-17. doi: 10.1093/nar/15.6.2707.
We have recently obtained 18 distinct cDNA clones representing different genes expressed in the early phase of EBV infection. One of them, c37, which is situated at the position 12907-122451 in the B95-8 viral genome, is shown here to code for a viral desoxyribonuclease [DNase]. Cell free translation of c37-selected messenger RNA yielded a protein of about 52 KDa which was immunoprecipitated by a high EA titer serum from nasopharyngeal carcinoma patient. This protein showed a DNase activity which was resistant to high salt concentrations (150 to 300 mM KCl) and was specifically neutralized by EA positive serum. These properties are typical of the EBV-specific DNase activity that we recently described in chemically induced EBV-transformed lymphoid cells. The same results were obtained on cell-free translation of the native RNA synthesized in vitro from pGEM-37 plasmid containing the entire c37 cDNA sequence (1.53 Kb). These data indicate that the BGLF5 open reading frame contained in c37 encodes for the EBV-specific DNase.
我们最近获得了18个不同的cDNA克隆,它们代表了在EBV感染早期表达的不同基因。其中一个名为c37的克隆,位于B95 - 8病毒基因组的12907 - 122451位置,此处显示其编码一种病毒脱氧核糖核酸酶[DNase]。对c37选择的信使RNA进行无细胞翻译产生了一种约52 kDa的蛋白质,该蛋白质被来自鼻咽癌患者的高滴度EA血清免疫沉淀。这种蛋白质表现出对高盐浓度(150至300 mM KCl)有抗性且能被EA阳性血清特异性中和的DNase活性。这些特性是我们最近在化学诱导的EBV转化淋巴细胞中描述的EBV特异性DNase活性的典型特征。从包含完整c37 cDNA序列(1.53 Kb)的pGEM - 37质粒体外合成的天然RNA进行无细胞翻译也得到了相同的结果。这些数据表明c37中包含的BGLF5开放阅读框编码EBV特异性DNase。