University of California San Diego, Department of Medicine, San Diego, CA 92093, USA; The Cancer Cell Map Initiative, San Francisco and La Jolla, CA, USA.
University of California San Francisco, Department of Cellular and Molecular Pharmacology, San Francisco, CA 94158, USA; The J. David Gladstone Institute of Data Science and Biotechnology, San Francisco, CA 94158, USA; Quantitative Biosciences Institute, University of California San Francisco, San Francisco, CA 94158, USA; The Cancer Cell Map Initiative, San Francisco and La Jolla, CA, USA; University of Texas Health Science Center San Antonio, Department of Biochemistry and Structural Biology, San Antonio, TX 78229, USA.
Cell Syst. 2023 Jun 21;14(6):447-463.e8. doi: 10.1016/j.cels.2023.04.007. Epub 2023 May 22.
The DNA damage response (DDR) ensures error-free DNA replication and transcription and is disrupted in numerous diseases. An ongoing challenge is to determine the proteins orchestrating DDR and their organization into complexes, including constitutive interactions and those responding to genomic insult. Here, we use multi-conditional network analysis to systematically map DDR assemblies at multiple scales. Affinity purifications of 21 DDR proteins, with/without genotoxin exposure, are combined with multi-omics data to reveal a hierarchical organization of 605 proteins into 109 assemblies. The map captures canonical repair mechanisms and proposes new DDR-associated proteins extending to stress, transport, and chromatin functions. We find that protein assemblies closely align with genetic dependencies in processing specific genotoxins and that proteins in multiple assemblies typically act in multiple genotoxin responses. Follow-up by DDR functional readouts newly implicates 12 assembly members in double-strand-break repair. The DNA damage response assemblies map is available for interactive visualization and query (ccmi.org/ddram/).
DNA 损伤反应 (DDR) 确保了 DNA 复制和转录的无差错进行,并且在许多疾病中被破坏。目前的一个挑战是确定协调 DDR 的蛋白质及其复合物的组织,包括组成性相互作用和对基因组损伤的反应。在这里,我们使用多条件网络分析来系统地在多个尺度上绘制 DDR 组装图。在有/没有遗传毒性暴露的情况下,对 21 种 DDR 蛋白进行亲和纯化,并与多组学数据相结合,揭示了 605 种蛋白质分为 109 个组装体的层次组织。该图谱捕获了典型的修复机制,并提出了新的 DDR 相关蛋白,这些蛋白延伸到应激、运输和染色质功能。我们发现,蛋白质组装与处理特定遗传毒性物质的特定遗传依赖性密切相关,并且多个组装体中的蛋白质通常在多种遗传毒性反应中起作用。通过 DDR 功能读出的后续研究,新发现了 12 个组装体成员参与双链断裂修复。DNA 损伤反应组装图谱可用于交互式可视化和查询(ccmi.org/ddram/)。