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ABSTRACT: Background
DNA double-strand breaks (DSBs) are the most lethal and dangerous type of lesions with significant implications for both cellular function and organismal health. The number of DSBs (NDSBs) across the genome reflects DNA damage severity. However, current quantification methods mainly rely on next-generation sequencing, which is laborious and expensive. This study aims to provide a simple, low-cost, and high-throughput standard curve-based method for quantifying genome-wide DSBs.Method
Genomic DNA from human, mouse, Arabidopsis, Saccharomyces cerevisiae, and Escherichia coli was digested by seven blunt-end restriction enzymes to generate DSB standards. Theoretical NDSBs for each standard were calculated based on restriction site frequency. Lig
SUBMITTER: Guo L
PROVIDER: S-EPMC12699195 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature