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Papers In Press, published online ahead of print July 6, 2004
MRC Virology Unit, Glasgow, Scotland G11 5JR
Corresponding Author: r.everett{at}vir.gla.ac.uk
Herpes simplex virus type 1 Immediate-Early regulatory protein ICP0 stimulates lytic infection and reactivation from latency, processes that require the ubiquitin E3 ligase activity mediated by the RING-finger domain in the N-terminal portion of the protein. ICP0 stimulates the production of polyubiquitin chains by the ubiquitin conjugating enzymes UbcH5a and UbcH6 in vitro, and in infected and transfected cells it induces the proteasome-dependent degradation of a number of cellular proteins including PML, the major constituent protein of PML nuclear bodies. However, ICP0 binds strongly to the cellular ubiquitin-specific protease USP7, a member of a family of proteins that cleave polyubiquitin chains and/or ubiquitin precursors. The region of ICP0 that is required for its interaction with USP7 has been mapped and mutations in this domain reduce the functionality of ICP0. These findings pose the question of why ICP0 includes domains that are associated with the potentially antagonistic functions of ubiquitin conjugation and deconjugation. Here we report that although neither protein affected the intrinsic activities of the other in vitro, USP7 protected ICP0 from auto-ubiquitination in vitro and their interaction can greatly increase the stability of ICP0 in vivo. These results demonstrate that RING-finger mediated auto-ubiquitination of ICP0 is physiologically relevant and can be regulated by interaction with USP7. This principle may extend to a number of cellular RING finger E3 ubiquitin ligase proteins that have analogous interactions with ubiquitin-specific cleavage enzymes.
J. Biol. Chem, 10.1074/jbc.M402885200
Submitted on March 15, 2004
Revised on July 6, 2004
Accepted on July 6, 2004
A RING finger ubiquitin ligase is protected from auto-catalyzed ubiquitination and degradation by binding to ubiquitin-specific protease USP7
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