Abstract DNA polymerase eta (Pol η) is a Y-family translesion polymerase responsible for synthesizing new DNA across UV-damaged templates. It is recruited to replication forks following mono-ubiquitination of the PCNA DNA clamp. This interaction is mediated by PCNA-interacting protein motifs within Pol η, as well as by its C-terminal ubiquitin-binding zinc finger (UBZ) domain. Previous work has suggested that Pol η itself is mono-ubiquitinated at four C-terminal lysine residues, which is dependent on prior ubiquitin-binding by its UBZ domain. Here, we show that Pol η can be modified at the same lysine residues by the ubiquitin-like protein, NEDD8. Like ubiquitination, this modification is driven by non-covalent interactions between NEDD8 and the UBZ domain. While only a small proportion of Pol η is mono-NEDDylated under normal conditions, these levels rapidly increase following inhibition of the COP9 signalosome, revealing that mono-NEDDylation is maintained under strong negative regulation. Finally, we demonstrate that mono-NEDDylation prevents Pol η foci formation in UV-C irradiated cells, suggesting that this modification prevents Pol η from participating in translesion DNA synthesis. These results thereby reveal a new mechanism by which human Pol η is regulated by ubiquitin-like proteins.
Moreno et al. (Wed,) studied this question.