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Exo1 competes with repair synthesis, converts NER intermediates to long ssDNA gaps, and promotes checkpoint activation.

Molecular cell | Oct 8, 2010

Ultraviolet (UV) light induces DNA-damage checkpoints and mutagenesis, which are involved in cancer protection and tumorigenesis, respectively. How cells identify DNA lesions and convert them to checkpoint-activating structures is a major question. We show that during repair of UV lesions in noncycling cells, Exo1-mediated processing of nucleotide excision repair (NER) intermediates competes with repair DNA synthesis. Impediments of the refilling reaction allow Exo1 to generate extended ssDNA gaps, detectable by electron microscopy, which drive Mec1 kinase activation and will be refilled by long-patch repair synthesis, as shown by DNA combing. We provide evidence that this mechanism may be stimulated by closely opposing UV lesions, represents a strategy to redirect problematic repair intermediates to alternative repair pathways, and may also be extended to physically different DNA damages. Our work has significant implications for understanding the coordination between repair of DNA lesions and checkpoint pathways to preserve genome stability.

Pubmed ID: 20932474 RIS Download

Mesh terms: Cell Cycle | Chromosomes, Fungal | DNA Damage | DNA Repair | DNA, Fungal | DNA, Single-Stranded | Dose-Response Relationship, Radiation | Enzyme Activation | Exodeoxyribonucleases | Gene Expression Regulation, Fungal | Genomic Instability | Intracellular Signaling Peptides and Proteins | Protein-Serine-Threonine Kinases | Saccharomyces cerevisiae | Saccharomyces cerevisiae Proteins | Time Factors | Ultraviolet Rays

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Associated grants

  • Agency: Telethon, Id: GGP030406

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