SUMO-modification and elimination of the active DNA demethylation enzyme TDG in cultured human cells

Abstract

Thymine DNA glycosylase (TDG) is a base excision repair enzyme that interacts with the small ubiquitin-related modifier (SUMO)-targeted ubiquitin E3 ligase RNF4 and functions in the active DNA demethylation pathway. Here we showed that both SUMOylated and non-modified forms of endogenous TDG fluctuated during the cell cycle and in response to drugs that perturbed cell cycle progression, including hydroxyurea and nocodazole. Additionally, we detected a SUMOylation-independent association between TDG and RNF4 in vitro as well as in vivo, and observed that both forms of TDG were efficiently degraded in RNF4-depleted cells when arrested at S phase. Our findings provide insights into the in vivo dynamics of TDG SUMOylation and further clarify the TDG-RNF4 interaction.

Keywords: Cell cycle; DNA demethylation; Ring finger protein 4 (RNF4); SUMO-targeted ubiquitin ligase (STUbL); Small ubiquitin-related modifier (SUMO); Thymine DNA glycosylase (TDG).