Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Mol Microbiol. 2021 Aug;116(2):707-722. doi: 10.1111/mmi.14765. Epub 2021 Jun 25.
During normal DNA replication, all cells encounter damage to their genetic material. As a result, organisms have developed response pathways that provide time for the cell to complete DNA repair before cell division occurs. In Bacillus subtilis, it is well established that the SOS-induced cell division inhibitor YneA blocks cell division after genotoxic stress; however, it remains unclear how YneA enforces the checkpoint. Here, we identify mutations that disrupt YneA activity and mutations that are refractory to the YneA-induced checkpoint. We find that YneA C-terminal truncation mutants and point mutants in or near the LysM peptidoglycan binding domain render YneA incapable of checkpoint enforcement. In addition, we develop a genetic method which isolated mutations in the ftsW gene that completely bypassed checkpoint enforcement while also finding that YneA interacts with late divisome components FtsL, Pbp2b, and Pbp1. Characterization of an FtsW variant resulted in considerably shorter cells during the DNA damage response indicative of hyperactive initiation of cell division and bypass of the YneA-enforced DNA damage checkpoint. With our results, we present a model where YneA inhibits septal cell wall synthesis by binding peptidoglycan and interfering with interaction between late arriving divisome components causing DNA damage checkpoint activation.
在正常的 DNA 复制过程中,所有细胞都会遇到其遗传物质的损伤。因此,生物体已经开发出了应对途径,以便在细胞分裂发生之前为细胞完成 DNA 修复提供时间。在枯草芽孢杆菌中,人们已经充分证实,SOS 诱导的细胞分裂抑制剂 YneA 在遗传毒性应激后阻止细胞分裂;然而,YneA 如何实施检查点仍然不清楚。在这里,我们鉴定出了破坏 YneA 活性的突变体和对 YneA 诱导的检查点无反应的突变体。我们发现,YneA C 端截断突变体和位于或靠近 LysM 肽聚糖结合结构域的点突变体使 YneA 无法实施检查点。此外,我们开发了一种遗传方法,该方法分离了 ftsW 基因中的突变体,这些突变体完全绕过了检查点的执行,同时还发现 YneA 与晚期分裂体成分 FtsL、Pbp2b 和 Pbp1 相互作用。对 FtsW 变体的特征分析表明,在 DNA 损伤反应期间细胞明显缩短,这表明细胞分裂的起始非常活跃,并且绕过了 YneA 实施的 DNA 损伤检查点。通过我们的结果,我们提出了一个模型,其中 YneA 通过结合肽聚糖抑制隔膜细胞壁的合成,并干扰晚期到达的分裂体成分之间的相互作用,从而导致 DNA 损伤检查点的激活。