Engineered chromatin readers track damaged chromatin dynamics in live cells and animals.
Ontology highlight
ABSTRACT: DNA damage is a constant threat to genome integrity and function. Diminished capacity for DNA repair is linked to many human diseases, therefore, understanding the molecular pathways responding to DNA damage is key for developing novel therapies. Lack of unbiased probes to report DNA damage dynamics in living cells and animals limits our current efforts to completely understand DNA repair processes. In this study, we overcome these limitations by engineering protein probes containing the tandem-BRCT domain of MCPH1, which we show to have a specific affinity for the DNA-damage-associated histone mark γH2AX. We employ these probes to track DNA damage dynamics in living cells exposed to a panel of different genotoxic insults, to visualize DNA damage targeted to heterochromatinised satellite r
SUBMITTER: da Silva RC
PROVIDER: S-EPMC12635110 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA