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The Fanconi anemia (FA) core complex promotes the tolerance/repair of DNA damage at stalled replication forks by catalyzing the monoubiquitination of FANCD2 and FANCI. Intriguingly, the core complex component FANCM also catalyzes branch migration of model Holliday junctions and replication forks in vitro. Here we have characterized the ortholog of FANCM in fission yeast Fml1 in order to understand the physiological significance of this activity. We show that Fml1 has at least two roles in homologous recombination-it promotes Rad51-dependent gene conversion at stalled/blocked replication forks and limits crossing over during mitotic double-strand break repair. In vitro Fml1 catalyzes both replication fork reversal and D loop disruption, indicating possible mechanisms by which it can fulfill its pro- and antirecombinogenic roles.

Original publication

DOI

10.1016/j.molcel.2008.08.024

Type

Journal article

Journal

Mol Cell

Publication Date

10/10/2008

Volume

32

Pages

118 - 128

Keywords

Crossing Over, Genetic, DNA Breaks, Double-Stranded, DNA Helicases, DNA Repair, DNA Replication, DNA, Cruciform, DNA, Fungal, Fanconi Anemia, Gene Conversion, Genes, Fungal, Humans, Mutation, Recombination, Genetic, Schizosaccharomyces, Schizosaccharomyces pombe Proteins