Lai M M, Patton C D, Baric R S, Stohlman S A
J Virol. 1983 Jun;46(3):1027-33. doi: 10.1128/JVI.46.3.1027-1033.1983.
To determine the structure and the mechanism of synthesis of mouse hepatitis virus mRNA, the map positions of the large RNase T1-resistant oligonucleotides of the seven mouse hepatitis virus strain A59 intracellular mRNA species were studied. We found that all but one of the oligonucleotides were mapped at the positions within each mRNA consistent with the nested-set, stairlike structure of mouse hepatitis virus mRNA (Lai et al., J. Virol. 39:823-834). However, one oligonucleotide, 10, was mapped near the 5' ends of every mRNA and virion genomic RNA. In other words, oligonucleotide 10 and, therefore, the sequences around the 5' ends of the mRNAs are not colinear with the genomic sequences. Because this oligonucleotide is present only once in the genomic RNA, this result indicates that oligonucleotide 10 is not transcribed from multiple sites on the genomic template, but rather represents a leader RNA sequence which is joined to the body sequences of the different mRNAs during mRNA transcription. This provides the most direct evidence thus far for the presence of leader sequences in the mRNAs of mouse hepatitis virus, which is a cytoplasmic virus. Several possible mechanisms of RNA synthesis are discussed.
为了确定小鼠肝炎病毒mRNA的结构和合成机制,我们研究了七种小鼠肝炎病毒A59株细胞内mRNA物种的大核糖核酸酶T1抗性寡核苷酸的图谱位置。我们发现,除了一个寡核苷酸外,所有寡核苷酸都定位在每个mRNA内的位置,这与小鼠肝炎病毒mRNA的嵌套集、阶梯状结构一致(Lai等人,《病毒学杂志》39:823 - 834)。然而,一个寡核苷酸,即寡核苷酸10,被定位在每个mRNA和病毒粒子基因组RNA的5'端附近。换句话说,寡核苷酸10以及因此mRNA 5'端周围的序列与基因组序列不共线。由于该寡核苷酸在基因组RNA中仅出现一次,这一结果表明寡核苷酸10不是从基因组模板上的多个位点转录而来,而是代表一个前导RNA序列,它在mRNA转录过程中与不同mRNA的主体序列相连。这为小鼠肝炎病毒(一种细胞质病毒)的mRNA中存在前导序列提供了迄今为止最直接的证据。文中讨论了几种可能的RNA合成机制。