Davis M G, Mar E C, Wu Y M, Huang E S
J Virol. 1984 Oct;52(1):129-35. doi: 10.1128/JVI.52.1.129-135.1984.
We constructed a DNA fragment map of low-passage Towne strain cytomegalovirus by analyzing cross-blot hybridization and hybridizations of isolated recombinant clones. The abundant late transcripts were located on this map by hybridization of labeled total RNA of virus-infected cells to blotted DNA fragments. The most abundant late transcript, carried by the 11.7-kilobase EcoRI fragment (EcoRI-G), was precisely mapped. The EcoRI fragment was fragmented and subcloned in a plasmid carrying simian virus 40 sequences (pSV-OH, constructed by Chi-Bom Chae, Department of Biochemistry, University of North Carolina, Chapel Hill). One resulting recombinant plasmid, pHD713SV2, was transferred to simian virus 40-transformed monkey kidney cells (COS-1) by DNA transfection. Synthesis of a cytomegalovirus-specific 67-kilodalton protein was detected in these cells by reaction of blotted proteins with virus-specific monoclonal antibody. The 67-kilodalton protein is a major phosphorylated protein found in virions; it is not glycosylated. The location of the gene for this 67-kilodalton protein is therefore assigned to the center of the L-unique region of human cytomegalovirus, at 0.37 to 0.39 map units.
我们通过分析交叉印迹杂交和分离的重组克隆的杂交,构建了低传代Towne株巨细胞病毒的DNA片段图谱。通过将病毒感染细胞的标记总RNA与印迹的DNA片段杂交,在该图谱上定位了丰富的晚期转录本。由11.7千碱基的EcoRI片段(EcoRI-G)携带的最丰富的晚期转录本被精确地定位。将EcoRI片段进行酶切并亚克隆到携带猴病毒40序列的质粒(pSV-OH,由北卡罗来纳大学教堂山分校生物化学系的池博·蔡构建)中。通过DNA转染将一个产生的重组质粒pHD713SV2转移到猴病毒40转化的猴肾细胞(COS-1)中。通过印迹蛋白与病毒特异性单克隆抗体的反应,在这些细胞中检测到巨细胞病毒特异性67千道尔顿蛋白的合成。67千道尔顿蛋白是在病毒粒子中发现的一种主要磷酸化蛋白;它不进行糖基化。因此,该67千道尔顿蛋白的基因位置被指定为人巨细胞病毒L-独特区域的中心,位于0.37至0.39个图谱单位处。