Department of Molecular and Cellular Biology, University of Geneva, 1211 Geneva 4, Switzerland.
Nucleic Acids Res. 2024 Sep 9;52(16):9654-9670. doi: 10.1093/nar/gkae658.
DNA-protein crosslinks (DPCs) challenge faithful DNA replication and smooth passage of genomic information. Our study unveils the cullin E3 ubiquitin ligase Rtt101 as a DPC repair factor. Genetic analyses demonstrate that Rtt101 is essential for resistance to a wide range of DPC types including topoisomerase 1 crosslinks, in the same pathway as the ubiquitin-dependent aspartic protease Ddi1. Using an in vivo inducible Top1-mimicking DPC system, we reveal the significant impact of Rtt101 ubiquitination on DPC removal across different cell cycle phases. High-throughput methods coupled with next-generation sequencing specifically highlight the association of Rtt101 with replisomes as well as colocalization with DPCs. Our findings establish Rtt101 as a main contributor to DPC repair throughout the yeast cell cycle.
DNA-蛋白质交联物(DPCs)对忠实的 DNA 复制和基因组信息的顺利传递构成挑战。我们的研究揭示了泛素连接酶 Rtt101 作为 DPC 修复因子的作用。遗传分析表明,Rtt101 对于抵抗多种 DPC 类型是必需的,包括拓扑异构酶 1 交联物,与依赖泛素的天冬氨酸蛋白酶 Ddi1 在同一途径中。利用体内诱导的拓扑异构酶 1 模拟 DPC 系统,我们揭示了 Rtt101 泛素化对不同细胞周期阶段 DPC 去除的显著影响。高通量方法与下一代测序相结合,特别突出了 Rtt101 与复制体的关联以及与 DPC 的共定位。我们的研究结果确立了 Rtt101 作为整个酵母细胞周期 DPC 修复的主要贡献者。