Wittek R, Cooper J A, Barbosa E, Moss B
Cell. 1980 Sep;21(2):487-93. doi: 10.1016/0092-8674(80)90485-7.
We have investigated the organization of transcriptional units within a 9000 bp segment of the terminally repeated region of the DNA genome of vaccinia virus, which uses its own enzyme system to synthesize mRNA within the cytoplasm of infected cells. RNA splicing, which has been demonstrated for DNA viruses that replicate within the nucleus of infected cells, does not appear to be involved in the formation of these first vaccinia virus mRNAs to be examined. Three immediate early mRNAs, approximately 1050, 600 and 1100 nucleotides long, were mapped between 3.21 and 4.24, 6.54 and 7.16, and 7.20 and 8.23 kb from the end of the genome, respectively. The direction of transcription was toward the end of the genome for the two larger mRNAs and in the opposite direction for the smallest one. Additional minor RNAs, which were larger in size, were mapped between and to the same DNA strand as the mRNAs of 1050 and 1100 nucleotides. No evidence for interrupted genes was obtained by nuclease S1 analysis after hybridization of RNA to labeled DNA. In addition, the 5' ends of the mRNAs, which were specifically labeled by in vitro capping, hybridized to DNA adjacent to the body of the message.
我们研究了痘苗病毒DNA基因组末端重复区域9000 bp片段内转录单元的组织情况,该病毒利用自身的酶系统在受感染细胞的细胞质中合成mRNA。对于在受感染细胞核内复制的DNA病毒已证实存在RNA剪接现象,但在这些首次检测的痘苗病毒mRNA的形成过程中似乎未涉及。三个立即早期mRNA,长度分别约为1050、600和1100个核苷酸,分别定位在距基因组末端3.21至4.24、6.54至7.16以及7.20至8.23 kb处。对于两个较大的mRNA,转录方向朝向基因组末端,而最小的那个mRNA转录方向相反。另外一些大小更大的次要RNA,定位在与1050和1100个核苷酸的mRNA相同的DNA链之间及该链上。RNA与标记DNA杂交后,经核酸酶S1分析未获得基因中断的证据。此外,通过体外加帽特异性标记的mRNA的5'末端,与紧邻信息主体的DNA杂交。