UBR5 interacts with the replication fork and protects DNA replication from DNA polymerase eta toxicity.

Accurate DNA replication is critical for the maintenance of genome integrity and cellular survival. Cancer-associated alterations often involve key players of DNA replication and of the DNA damage-signalling cascade. Post-translational modifications play a fundamental role in coordinating replication and repair and central among them is ubiquitylation. We show that the E3 ligase UBR5 interacts with components of the replication fork, including the translesion synthesis (TLS) polymerase pol?. Depletion of UBR5 leads to replication problems, such as slower S-phase progression, resulting in the accumulation of single stranded DNA. The effect of UBR5 knockdown is related to a mis-regulation in the pathway that controls the ubiquitylation of histone H2A (UbiH2A) and blocking this modification is sufficient to rescue the cells from replication problems. We show that the presence of pol eta is the main cause of replication defects and cell death when UBR5 is silenced. Finally, we unveil a novel interaction between pol eta and H2A suggesting that UbiH2A could be involved in pol? recruitment to the chromatin and the regulation of TLS.