 | | Rad51 filaments assembled in the absence of the complex formed by the Rad51 paralogs Rad55 and Rad57 are outcompeted by translesion DNA polymerases on UV-induced ssDNA gaps | Maloisel L., Ma E., Phipps J., Deshayes A., Mattarocci S., Marcand S., Dubrana K., Coïc E. | | | | | Molecular basis of the dual role of the Mlh1-Mlh3 endonuclease in MMR and in meiotic crossover formation. | Dai J, Sanchez A, Adam C, Ranjha L, Reginato G, Chervy P, Tellier-Lebegue C, Andreani J, Guérois R, Ropars V, Le Du MH, Maloisel L, Martini E, Legrand P, Thureau A, Cejka P, Borde V, Charbonnier JB. | | | | | Rad52 Oligomeric N-Terminal Domain Stabilizes Rad51 Nucleoprotein Filaments and Contributes to Their Protection against Srs2 | Ma, E., Maloisel, L., Le Falher, L., Guérois, R., Coïc, E | | | | | Rad52-Rad51 association is essential to protect Rad51 filaments against Srs2, but facultative for filament formation | Ma E, Dupaigne P,Maloisel L, Guerois R, Le Cam E, Coïc E. | | | | | The translesion DNA polymerases Pol Zeta and Rev1 are activated independently of PCNA ubiquitination upon UV radiation in mutants of DNA polymerase Delta | Tellier-Lebegue C, Dizet E, Ma E, Veaute X, Coïc E, Charbonnier JB, Maloisel L | | | | | Rad52 Sumoylation Prevents the Toxicity of Unproductive Rad51 Filaments Independently of the Anti-Recombinase Srs2 | Esta A, Ma E, Dupaigne P, Maloisel L, Guerois R, Le Cam E, Veaute X, Coic E | | | | | Regulation of budding yeast mating-type switching donor preference by the FHA domain of Fkh1. | Li J, Coïc E, Lee K, Lee CS, Kim JA, Wu Q , Haber JE | | | | | Stable interactions between DNA polymerase delta catalytic and structural subunits are essential for efficient DNA repair | Brocas C, Charbonnier J B, Dherin C, Gangloff S, Maloisel L | | | | | DNA polymerase delta is preferentially recruited during homologous recombination to promote heteroduplex DNA extension | Maloisel L, Fabre F, Gangloff S | | |
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