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Orchestration of the DNA-damage response by the RNF8 ubiquitin ligase.

Science (New York, N.Y.) | Dec 7, 2007

http://www.ncbi.nlm.nih.gov/pubmed/18006705

Cells respond to DNA double-strand breaks by recruiting factors such as the DNA-damage mediator protein MDC1, the p53-binding protein 1 (53BP1), and the breast cancer susceptibility protein BRCA1 to sites of damaged DNA. Here, we reveal that the ubiquitin ligase RNF8 mediates ubiquitin conjugation and 53BP1 and BRCA1 focal accumulation at sites of DNA lesions. Moreover, we establish that MDC1 recruits RNF8 through phosphodependent interactions between the RNF8 forkhead-associated domain and motifs in MDC1 that are phosphorylated by the DNA-damage activated protein kinase ataxia telangiectasia mutated (ATM). We also show that depletion of the E2 enzyme UBC13 impairs 53BP1 recruitment to sites of damage, which suggests that it cooperates with RNF8. Finally, we reveal that RNF8 promotes the G2/M DNA damage checkpoint and resistance to ionizing radiation. These results demonstrate how the DNA-damage response is orchestrated by ATM-dependent phosphorylation of MDC1 and RNF8-mediated ubiquitination.

Pubmed ID: 18006705 RIS Download

Mesh terms: Amino Acid Motifs | Amino Acid Sequence | Ataxia Telangiectasia Mutated Proteins | BRCA1 Protein | Cell Cycle Proteins | Cell Line, Tumor | Cell Nucleus Structures | DNA Breaks, Double-Stranded | DNA Repair | DNA-Binding Proteins | HeLa Cells | Humans | Intracellular Signaling Peptides and Proteins | Molecular Sequence Data | Nuclear Proteins | Phosphorylation | Protein Structure, Tertiary | Protein-Serine-Threonine Kinases | RNA, Small Interfering | Trans-Activators | Tumor Suppressor Proteins | Ubiquitin | Ubiquitin-Conjugating Enzymes | Ubiquitin-Protein Ligases | Ubiquitination

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