Changes in DNA double-strand break repair during aging correlate with an increase in genomic mutations

Author:

Mojumdar AdityaORCID,Mair Nicola,Adam Nancy,Cobb Jennifer A.

Abstract

AbstractA double -strand break (DSB) is one of the most deleterious forms of DNA damage. In eukaryotic cells, two main repair pathways have evolved to repair DSBs, homologous recombination (HR) and non-homologous end-joining (NHEJ). HR is the predominant pathway of repair in the unicellular eukaryotic organism, S. cerevisiae. However, during replicative aging the relative use of HR and NHEJ shifts in favor of end-joining repair. By monitoring repair events in the HO-DSB system, we find that early in replicative aging there is a decrease in the association of long-range resection factors, Dna2-Sgs1 and Exo1 at the break site and a decrease in DNA resection. Subsequently, as aging progressed, the recovery of Ku70 at DSBs decreased and the break site associated with the nuclear pore complex at the nuclear periphery, which is the location where DSB repair occurs through alternative pathways that are more mutagenic. End-bridging remained intact as HR and NHEJ declined, but eventually it too became disrupted in cells at advanced replicative age. In all, our work provides insight into the molecular changes in DSB repair pathway during replicative aging. HR first declined, resulting in a transient increase in the NHEJ. However, with increased cellular divisions, Ku70 recovery at DSBs and NHEJ subsequently declined. In wild type cells of advanced replicative age, there was a high frequency of repair products with genomic deletions and microhomologies at the break junction, events not observed in young cells which repaired primarily by HR.HighlightsDecreased DNA resection at DSBs is an early event of replicative agingEnd-joining repair increases as resection decreases at DSBs in older cellsIn older cells the products of DSB repair contain deletions and microhomologiesDSBs associate with the NPC at the nuclear periphery more in older cellsOld Cell Enrichment method suitable for molecular biology approaches in budding yeast

Publisher

Cold Spring Harbor Laboratory

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Interdependence between Nuclear Pore Gatekeepers and Genome Caretakers: Cues from Genome Instability Syndromes;International Journal of Molecular Sciences;2024-08-29

2. Genomic Instability and Epigenetic Changes during Aging;International Journal of Molecular Sciences;2023-09-19

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