Abstract
AbstractThe recent discovery of non-proteinaceous ubiquitylation substrates broadened our understanding of this modification beyond conventional protein targets. However, the existence of additional types of substrates remains elusive. Here, we present evidence that nucleic acids can also be directly ubiquitylated via ester bond formation. DTX3L, a member of the DELTEX family E3 ubiquitin ligases, ubiquitylates DNA and RNA in vitro and that this activity is shared with DTX3, but not with the other DELTEX family members DTX1, DTX2 and DTX4. DTX3L shows preference for the 3′-terminal adenosine over other nucleotides. In addition, we demonstrate that ubiquitylation of nucleic acids is reversible by DUBs such as USP2, JOSD1 and SARS-CoV-2 PLpro. Overall, our study proposes reversible ubiquitylation of nucleic acids in vitro and discusses its potential functional implications.
Funder
Wellcome Trust
UKRI | Biotechnology and Biological Sciences Research Council
Ovarian Cancer Research Alliance
Oxford University Challenge Seed Fund
Cancer Research UK
Edward Penley Abraham Research Fund
EC | European Research Council
la Ligue contre le Cancer
Oxford University Press John Fell Research Fund
University of Oxford Medical Sciences Division Pump Priming Award
Publisher
Springer Science and Business Media LLC