Kim Seong Min, Forsburg Susan L
Program in Molecular & Computational Biology, University of Southern California, Los Angeles, CA 90089, USA.
Genes (Basel). 2018 Dec 14;9(12):634. doi: 10.3390/genes9120634.
Replication stress results in various forms of aberrant replication intermediates that need to be resolved for faithful chromosome segregation. Structure-specific endonucleases (SSEs) recognize DNA secondary structures rather than primary sequences and play key roles during DNA repair and replication stress. Holliday junction resolvase MUS81 (methyl methane sulfonate (MMS), and UV-sensitive protein 81) and XPF (xeroderma pigmentosum group F-complementing protein) are a subset of SSEs that resolve aberrant replication structures. To ensure genome stability and prevent unnecessary DNA breakage, these SSEs are tightly regulated by the cell cycle and replication checkpoints. We discuss the regulatory network that control activities of MUS81 and XPF and briefly mention other SSEs involved in the resolution of replication intermediates.
复制应激会导致各种形式的异常复制中间体,为了实现准确的染色体分离,这些中间体需要得到解决。结构特异性核酸内切酶(SSEs)识别DNA二级结构而非一级序列,并在DNA修复和复制应激过程中发挥关键作用。霍利迪连接体解离酶MUS81(甲磺酸甲酯(MMS)和紫外线敏感蛋白81)和XPF(着色性干皮病F组互补蛋白)是解决异常复制结构的SSEs的一个子集。为确保基因组稳定性并防止不必要的DNA断裂,这些SSEs受到细胞周期和复制检查点的严格调控。我们讨论了控制MUS81和XPF活性的调控网络,并简要提及了参与复制中间体解决的其他SSEs。