Department of Biology, Indiana University, Bloomington, IN, 47405, USA.
Luddy School of Informatics, Computing and Engineering, Indiana University, Bloomington, IN, 47405, USA.
DNA Repair (Amst). 2020 Jun;90:102852. doi: 10.1016/j.dnarep.2020.102852. Epub 2020 Apr 18.
When its DNA is damaged, Escherichia coli induces the SOS response, which consists of about 40 genes that encode activities to repair or tolerate the damage. Certain alleles of the major SOS-control genes, recA and lexA, cause constitutive expression of the response, resulting in an increase in spontaneous mutations. These mutations, historically called "untargeted", have been the subject of many previous studies. Here we re-examine SOS-induced mutagenesis using mutation accumulation followed by whole-genome sequencing (MA/WGS), which allows a detailed picture of the types of mutations induced as well as their sequence-specificity. Our results confirm previous findings that SOS expression specifically induces transversion base-pair substitutions, with rates averaging about 60-fold above wild-type levels. Surprisingly, the rates of G:C to C:G transversions, normally an extremely rare mutation, were induced an average of 160-fold above wild-type levels. The SOS-induced transversion showed strong sequence specificity, the most extreme of which was the G:C to C:G transversions, 60% of which occurred at the middle base of 5'GGC3'+5'GCC3' sites, although these sites represent only 8% of the G:C base pairs in the genome. SOS-induced transversions were also DNA strand-biased, occurring, on average, 2- to 4- times more often when the purine was on the leading-strand template and the pyrimidine on the lagging-strand template than in the opposite orientation. However, the strand bias was also sequence specific, and even of reverse orientation at some sites. By eliminating constraints on the mutations that can be recovered, the MA/WGS protocol revealed new complexities of SOS "untargeted" mutations.
当大肠杆菌的 DNA 受损时,会诱导 SOS 反应,该反应由大约 40 个基因组成,这些基因编码修复或耐受损伤的活性。SOS 控制基因主要等位基因 recA 和 lexA 的某些等位基因导致该反应的组成型表达,从而导致自发突变的增加。这些突变,历史上称为“非靶向”,一直是许多先前研究的主题。在这里,我们使用突变积累和全基因组测序(MA/WGS)重新检查 SOS 诱导的突变,这允许详细了解诱导的突变类型及其序列特异性。我们的结果证实了先前的发现,即 SOS 表达特异性诱导颠换碱基对替换,其速率平均比野生型水平高出约 60 倍。令人惊讶的是,通常极为罕见的 G:C 到 C:G 颠换的速率平均比野生型水平高出 160 倍。SOS 诱导的颠换具有很强的序列特异性,其中最极端的是 G:C 到 C:G 颠换,其中 60%发生在 5'GGC3'+5'GCC3' 位点的中间碱基上,尽管这些位点仅占基因组中 G:C 碱基对的 8%。SOS 诱导的颠换也具有 DNA 链偏向性,当嘌呤位于前导链模板上且嘧啶位于滞后链模板上时,平均发生的频率比相反方向高 2-4 倍。然而,链偏向性也是序列特异性的,甚至在某些位点是反向的。通过消除可以恢复的突变的限制,MA/WGS 方案揭示了 SOS“非靶向”突变的新复杂性。