Department of Respiratory Diseases, Qingdao Haici Hospital, Qingdao, Shandong, China.
Future Microbiol. 2020 Sep;15:1343-1352. doi: 10.2217/fmb-2020-0149.
The inference of coronavirus evolution is largely based on mutations in SARS-CoV-2 genome. Misinterpretation of these mutations would mislead people about the evolution of SARS-CoV-2. With 4521 lines of SARS-CoV-2, we obtained 3169 unique point mutation sites. We counted the numbers and calculated the minor allele frequency (MAF) of each mutation type. Nearly half of the point mutations are C-T mismatches and 20% are A-G mismatches. The MAF of C-T and A-G mismatches is significantly higher than MAF of other mutation types. The excessive C-T mismatches do not resemble the random mutation profile. They are likely to be caused by the cytosine-to-uridine deamination system in hosts.
冠状病毒的进化推断在很大程度上基于 SARS-CoV-2 基因组中的突变。对这些突变的误解会导致人们对 SARS-CoV-2 的进化产生误解。我们从 4521 条 SARS-CoV-2 序列中获得了 3169 个独特的点突变位点。我们统计了每种突变类型的数量并计算了其次要等位基因频率(MAF)。近一半的点突变是 C-T 错配,20%是 A-G 错配。C-T 和 A-G 错配的 MAF 明显高于其他突变类型的 MAF。过多的 C-T 错配与随机突变模式不相似。它们可能是由宿主中的胞嘧啶到尿嘧啶脱氨酶系统引起的。