Suppr超能文献

利用互补DNA鉴定爱泼斯坦-巴尔病毒特异性脱氧核糖核酸酶基因

Identification of an Epstein-Barr virus-specific desoxyribonuclease gene using complementary DNA.

作者信息

Zhang C X, Decaussin G, de Turenne Tessier M, Daillie J, Ooka T

出版信息

Nucleic Acids Res. 1987 Mar 25;15(6):2707-17. doi: 10.1093/nar/15.6.2707.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009c/340679/179bec595edf/nar00250-0309-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验