Inhibition of topoisomerase I prevents chromosome breakage at common fragile sites.

Martin F Arlt, Thomas W Glover

Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA. arltm@umich.edu

DNA repair 2010 Jun 4

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Common fragile sites are loci that preferentially form gaps and breaks on metaphase chromosomes when DNA synthesis is perturbed, particularly after treatment with the DNA polymerase inhibitor, aphidicolin. We and others have identified several cell cycle checkpoint and DNA repair proteins that influence common fragile site stability. However, the initial events underlying fragile site breakage remain poorly understood. We demonstrate here that aphidicolin-induced gaps and breaks at fragile sites are prevented when cells are co-treated with low concentrations of the topoisomerase I inhibitor, camptothecin. This reduction in breakage is accompanied by a reduction in aphidicolin-induced RPA foci, CHK1 and RPA2 phosphorylation, and PCNA monoubiquitination, indicative of reduced levels of single stranded DNA. Furthermore, camptothecin reduces spontaneous fragile site breakage seen in cells lacking ATR, even in the absence of aphidicolin. These data from cultured human cells demonstrate that topoisomerase I activity is required for DNA common fragile site breaks and suggest that polymerase-helicase uncoupling is a key initial event in this process. Copyright 2010 Elsevier B.V. All rights reserved.

Citation

Martin F Arlt, Thomas W Glover. Inhibition of topoisomerase I prevents chromosome breakage at common fragile sites. DNA repair. 2010 Jun 4;9(6):678-89