Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Mol Cell. 2021 Feb 18;81(4):649-658. doi: 10.1016/j.molcel.2021.01.012. Epub 2021 Jan 29.
Accurate DNA replication is constantly threatened by DNA lesions arising from endogenous and exogenous sources. Specialized DNA replication stress response pathways ensure replication fork progression in the presence of DNA lesions with minimal delay in fork elongation. These pathways broadly include translesion DNA synthesis, template switching, and replication fork repriming. Here, we discuss recent advances toward our understanding of the mechanisms that regulate the fine-tuned balance between these different replication stress response pathways. We also discuss the molecular pathways required to fill single-stranded DNA gaps that accumulate throughout the genome after repriming and the biological consequences of using repriming instead of other DNA damage tolerance pathways on genome integrity and cell fitness.
准确的 DNA 复制不断受到内源性和外源性来源的 DNA 损伤的威胁。专门的 DNA 复制应激反应途径确保在 DNA 损伤存在的情况下复制叉的进展,最小化叉延伸的延迟。这些途径广泛包括跨损伤 DNA 合成、模板转换和复制叉重新启动。在这里,我们讨论了在理解调节这些不同的复制应激反应途径之间的精细平衡的机制方面的最新进展。我们还讨论了在重新启动后填补整个基因组中单链 DNA 缺口所需的分子途径,以及使用重新启动而不是其他 DNA 损伤容忍途径对基因组完整性和细胞适应性的生物学后果。