Department of Biology, University of Iowa, Iowa City, IA 52245, USA.
Department of Cancer Genetics and Epigenetics, City of Hope, Duarte, CA 91010, USA.
Nucleic Acids Res. 2022 Jul 8;50(12):6870-6889. doi: 10.1093/nar/gkac520.
Break-induced replication (BIR) proceeds via a migrating D-loop for hundreds of kilobases and is highly mutagenic. Previous studies identified long single-stranded (ss) nascent DNA that accumulates during leading strand synthesis to be a target for DNA damage and a primary source of BIR-induced mutagenesis. Here, we describe a new important source of mutagenic ssDNA formed during BIR: the ssDNA template for leading strand BIR synthesis formed during D-loop migration. Specifically, we demonstrate that this D-loop bottom template strand (D-BTS) is susceptible to APOBEC3A (A3A)-induced DNA lesions leading to mutations associated with BIR. Also, we demonstrate that BIR-associated ssDNA promotes an additional type of genetic instability: replication slippage between microhomologies stimulated by inverted DNA repeats. Based on our results we propose that these events are stimulated by both known sources of ssDNA formed during BIR, nascent DNA formed by leading strand synthesis, and the D-BTS that we describe here. Together we report a new source of mutagenesis during BIR that may also be shared by other homologous recombination pathways driven by D-loop repair synthesis.
断裂诱导复制 (BIR) 通过迁移的 D 环进行,可延伸数百千碱基,且具有高度突变性。先前的研究表明,在先导链合成过程中积累的长单链 (ss) 新生 DNA 是 DNA 损伤的靶标,也是 BIR 诱导突变的主要来源。在这里,我们描述了 BIR 过程中形成的一种新的重要突变性 ssDNA 来源:D 环迁移过程中形成的先导链 BIR 合成的 ssDNA 模板。具体来说,我们证明了这种 D 环底部模板链 (D-BTS) 易受 APOBEC3A (A3A) 诱导的 DNA 损伤,从而导致与 BIR 相关的突变。此外,我们还证明了 BIR 相关的 ssDNA 促进了另一种类型的遗传不稳定性:由倒置 DNA 重复序列刺激的微同源性之间的复制滑动。基于我们的结果,我们提出这些事件受到 BIR 过程中形成的两种已知 ssDNA 来源的刺激,一种是由先导链合成形成的新生 DNA,另一种是我们在这里描述的 D-BTS。我们共同报告了 BIR 过程中一种新的突变来源,它也可能被其他由 D 环修复合成驱动的同源重组途径共享。