Genome-wide kinetics of DNA excision repair in relation to chromatin state and mutagenesis

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 113; no. 15; pp. E2124 - E2133
• Main Authors: Adar, Sheera, Hu, Jinchuan, Lieb, Jason D., Sancar, Aziz
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 12.04.2016; National Acad Sciences
• Series: PNAS Plus
• Subjects: Biological Sciences; Cancer; Carcinogenesis; Cell Line; Chromatin; Chromatin - genetics; Deoxyribonucleic acid; DNA; DNA Repair - genetics; Genome, Human - genetics; Genomes; Humans; Irradiation; Kinetics; Melanoma - genetics; Mutagenesis; Mutagenesis - genetics; PNAS Plus; Risk assessment; Sequence Analysis, DNA - methods; Ultraviolet radiation; Ultraviolet Rays - adverse effects; mutation; transcription; chromatin; DNA repair; DNA damage
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1603388113

We recently developed a high-resolution genome-wide assay for mapping DNA excision repair named eXcision Repair-sequencing (XR-seq) and have now used XR-seq to determine which regions of the genome are subject to repair very soon after UV exposure and which regions are repaired later. Over a time course, we measured repair of the UV-induced damage of cyclobutane pyrimidine dimers (CPDs) (at 1, 4, 8, 16, 24, and 48 h) and (6-4)pyrimidine-pyrimidone photoproducts [(6-4)PPs] (at 5 and 20 min and 1, 2, and 4 h) in normal human skin fibroblasts. Each type of damage has distinct repair kinetics. The (6-4)PPs are detected as early as 5 min after UV treatment, with the bulk of repair completed by 4 h. Repair of CPDs, which we previously showed is intimately coupled to transcription, is slower and in certain regions persists even 2 d after UV irradiation. We compared our results to the Encyclopedia of DNA Elements data regarding histone modifications, chromatin state, and transcription. For both damage types, and for both transcription-coupled and general excision repair, the earliest repair occurred preferentially in active and open chromatin states. Conversely, repair in regions classified as “heterochromatic” and “repressed” was relatively low at early time points, with repair persisting into the late time points. Damage that remains during DNA replication increases the risk for mutagenesis. Indeed, laterepaired regions are associated with a higher level of cancer-linked mutations. In summary, we show that XR-seq is a powerful approach for studying relationships among chromatin state, DNA repair, genome stability, mutagenesis, and carcinogenesis.