Disa limits recg activities at stalled or reversed replication forks

Abstract

The DNA damage checkpoint protein DisA and the branch migration translocase RecG are implicated in the preservation of genome integrity in reviving haploid Bacillus subtilis spores. DisA synthesizes the essential cyclic 3′, 5′‐diadenosine monophosphate (c‐di‐AMP) second messenger and such synthesis is suppressed upon replication perturbation. In vitro, c‐di‐AMP synthesis is suppressed when DisA binds DNA structures that mimic stalled or reversed forks (gapped forks or Holliday junctions [HJ]). RecG, which does not form a stable complex with DisA, unwinds branched intermediates, and in the presence of a limiting ATP concentration and HJ DNA, it blocks DisA-mediated c‐di‐AMP synthesis. DisA pre‐bound to a stalled or reversed fork limits RecG‐mediated ATP hydrolysis and DNA unwinding, but not if RecG is pre‐bound to stalled or reversed forks. We propose that RecG‐mediated fork remodeling is a genuine in vivo activity, and that DisA, as a molecular switch, limits RecG‐mediated fork reversal and fork restoration. DisA and RecG might provide more time to process perturbed forks, avoiding genome breakage.