Laboratory of Emerging Pathogens, Division of Transfusion-Transmitted Diseases, Food and Drug Administration, Bethesda, Maryland 20892, USA.
Viruses. 2013 Jan 18;5(1):279-94. doi: 10.3390/v5010279.
In previous studies, differences in the amount of genomic and subgenomic RNA produced by coronaviruses with mutations in the programmed ribosomal frameshift signal of ORF1a/b were observed. It was not clear if these differences were due to changes in genomic sequence, the protein sequence or the frequency of frameshifting. Here, viruses with synonymous codon changes are shown to produce different ratios of genomic and subgenomic RNA. These findings demonstrate that the protein sequence is not the primary cause of altered genomic and subgenomic RNA production. The synonymous codon changes affect both the structure of the frameshift signal and frameshifting efficiency. Small differences in frameshifting efficiency result in dramatic differences in genomic RNA production and TCID50 suggesting that the frameshifting frequency must stay above a certain threshold for optimal virus production. The data suggest that either the RNA sequence or the ratio of viral proteins resulting from different levels of frameshifting affects viral replication.
在之前的研究中,观察到 ORF1a/b 的程序性核糖体移码信号发生突变的冠状病毒产生的基因组和亚基因组 RNA 的量存在差异。尚不清楚这些差异是否归因于基因组序列、蛋白质序列或移码频率的改变。在这里,显示具有同义密码子变化的病毒产生不同比例的基因组和亚基因组 RNA。这些发现表明蛋白质序列不是改变基因组和亚基因组 RNA 产生的主要原因。同义密码子变化影响移码信号的结构和移码效率。移码效率的微小差异导致基因组 RNA 产生和 TCID50 的显著差异,这表明移码频率必须保持在一定的阈值以上,以实现最佳病毒产生。数据表明,不同水平移码产生的 RNA 序列或病毒蛋白的比例会影响病毒复制。