Human RAD52 Captures and Holds DNA Strands, Increases DNA Flexibility, and Prevents Melting of Duplex DNA: Implications for DNA Recombination

Ineke Brouwer, Hongshan Zhang, Andrea Candelli, Davide Normanno, Erwin J. G. Peterman, Gijs J. L. Wuite, Mauro Modesti

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Human RAD52 promotes annealing of complementary single-stranded DNA (ssDNA). In-depth knowledge of RAD52-DNA interaction is required to understand how its activity is integrated in DNA repair processes. Here, we visualize individual fluorescent RAD52 complexes interacting with single DNA molecules. The interaction with ssDNA is rapid, static, and tight, where ssDNA appears to wrap around RAD52 complexes that promote intra-molecular bridging. With double-stranded DNA (dsDNA), interaction is slower, weaker, and often diffusive. Interestingly, force spectroscopy experiments show that RAD52 alters the mechanics dsDNA by enhancing DNA flexibility and increasing DNA contour length, suggesting intercalation. RAD52 binding changes the nature of the overstretching transition of dsDNA and prevents DNA melting, which is advantageous for strand clamping during or after annealing. DNA-bound RAD52 is efficient at capturing ssDNA in trans. Together, these effects may help key steps in DNA repair, such as second-end capture during homologous recombination or strand annealing during RAD51-independent recombination reactions.

Original languageEnglish
Pages (from-to)2845-2853
Number of pages9
JournalCell Reports
Volume18
Issue number12
DOIs
Publication statusPublished - 21 Mar 2017

Funding

We thank Claire Wyman, Bertrand Llorente, and Murray Junop for critical reading of the manuscript. This work was supported by the French National Research Agency (project RADORDER ANR-10-BLAN-1521; to M.M.), the ARC Foundation for Cancer Research (to M.M.), the A∗MIDEX project (no. ANR-11-IDEX-0001-02) for the «Investissements d'Avenir» French Government program (to M.M.), funding from LASERLAB-EUROPE (grant agreement no. 284464; EC's Seventh Framework Programme; to M.M.), a fellowship from the Collège of Aix-Marseille Université (to H.Z.), a VICI grant of the Nederlandse Organisatie voor Wetenschappelijk Onderzoek (to G.J.L.W.), and a European Research Council starting grant (no. 260849-PhysGene; to G.J.L.W.).

FundersFunder number
Collège of Aix-Marseille Université
Seventh Framework Programme260849, 284464
Laserlab-Europe
European Research Council
Agence Nationale de la RechercheANR-10-BLAN-1521
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Fondation ARC pour la Recherche sur le CancerANR-11-IDEX-0001-02
Seventh Framework Programme

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