Nature CommunicationsCancer BiologyPeer-reviewed journal article
Hierarchical determinants of the oxidation-induced mutational landscape in human cells.
Cameron CorderoiD, Kavi P.M. MehtaiD, Tyler WeaveriD, Justin A. LingiD, B. D. FreudenthaliD, David CorteziD, Steven A. RobertsiD
Abstract
8-oxoguanine (8-oxoG) is a common oxidative DNA lesion, which causes G>T substitutions that compose COSMIC single base substitution signature 18 (SBS18) in human cancers. Determinants of local and regional differences in 8-oxoG-induced mutability are currently unknown. To uncover factors influencing the topology of 8-oxoG-induced mutations, we assessed spontaneous and KBrO3-induced 8-oxoG mutagenesis in human cell lines. KBrO3 exposure produced a SBS18-like substitution spectrum and a distinct never-before reported INDEL signature that we also observed in human cancers. KBrO3-induced 8-oxoG lesions occurred with similar sequence preference as KBrO3-induced substitutions, indicating that the reactivity of specific reactive oxygen species (ROS) dictates the trinucleotide motif specificity for 8-oxoG-induced mutagenesis. While 8-oxoG lesions occurred relatively uniformly across chromatin states and nucleosomes, 8-oxoG-induced mutations occurred more frequently in more compact regions of the genome, within nucleosomal DNA, and at inward facing guanines within strongly positioned nucleosomes. Cryo-EM structures of OGG1 bound to nucleosomes indicate that these effects originate from OGG1s ability to flip outward positioned 8-oxoG lesions into the catalytic pocket with only minor alterations to nucleosome structure, while inward facing lesions occluded by the histone octamer are unrecognized. Mutation spectra from cells with DNA repair deficiencies revealed a hierarchical DNA repair network limiting 8-oxoG mutagenesis in human cells, where OGG1- and MUTY-mediated BER is supplemented by replication-associated factors participating in tolerance of 8-oxoG or derived repair intermediates (i.e. Pol {eta} and HMCES). Surprisingly, analysis of transcriptional asymmetry of KBrO3-induced mutations demonstrated transcription-coupled repair of 8-oxoG in Pol {eta}-deficient cells. Thus, radical chemistry, chromatin structures, and DNA repair processes combine to dictate the oxidative mutational landscape in human genomes.
- organism: human
- assay: DNA methylation
- assay: whole-genome sequencing
- research focus: chromatin & epigenetic regulation
- research focus: cell type annotation
- approach: experimental assay
- Citations
- 35
- FWCI
- 3.89
- Field percentile
- top 4%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Structure, dynamics, and processing of 8oxoG:A in the nucleosome
Abigayle F. Vito, Justin A. Ling, … Bret Freudenthal·bioRxiv·Sep 2, 2025
- Systematic mutagenesis assay promotes comprehension of the strand-bias laws for mutations induced by oxidative DNA damage
- Molecular mechanisms associated with clustered lesion-induced impairment of 8-oxoG recognition by the human glycosylase OGG1
- MUTYH activity maintains telomere stability in response to chronic telomeric 8-oxoguanine damage in cancer cells
Mariarosaria De Rosa, Theresa M. Heidenreich, … Patricia Lynn Opresko·BiomoleculesPeer-reviewed·Aug 26, 2026
- Genomic landscape of oxidative DNA damage and repair reveals regioselective protection from mutagenesis
Anna R. Poetsch, Simon J. Boulton, Nicholas M. Luscombe·Genome biologyPeer-reviewed·Dec 1, 2018
- Genomic 8-oxoguanine modulates gene transcription independent of its repair by DNA glycosylases OGG1 and MUTYH
Tobias Obermann, Teri Sakshaug, … Katja Scheffler·Redox BiologyPeer-reviewed·Dec 5, 2024