When damaged DNA is replicated, gaps can be left behind in the replicated DNA. Two processes, recombinational repair or post-replication repair (PRR), were thought to act independently in gap filling. This study defines how the error-free branch of PRR is involved in lesion bypass and finds that when the replicative clamp PCNA is SUMO modified, Rad18 and Rad5 are able to promote polyubiquitination of PCNA.
- Dana Branzei
- Fabio Vanoli
- Marco Foiani