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American Association for the Advancement of Science, Science, 6038(333), p. 84-87, 2011

DOI: 10.1126/science.1204258

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Mechanism of RAD51dependent DNA interstrand crosslink repair

Journal article published in 2011 by David T. Long, Markus Räschle, Vladimir Joukov, Johannes C. Walter
This paper is available in a repository.
This paper is available in a repository.

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Abstract

DNA interstrand cross-links (ICLs) are toxic DNA lesions whose repair in S phase of eukaryotic cells is incompletely understood. In Xenopus egg extracts, ICL repair is initiated when two replication forks converge on the lesion. Dual incisions then create a DNA double-strand break (DSB) in one sister chromatid while lesion bypass restores the other sister. We report that the broken sister chromatid is repaired via RAD51-dependent strand invasion into the regenerated sister. Recombination acts downstream of FANCI-FANCD2, yet RAD51 binds ICL-stalled replication forks independently of FANCI-FANCD2 and prior to DSB formation. Our results elucidate the functional relationship between the Fanconi anemia pathway and the recombination machinery during ICL repair. In addition, they demonstrate the complete repair of a DSB via homologous recombination in vitro.