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The ubiquitin-specific protease USP7 Modulates the replication of kaposi's sarcoma-associated herpesvirus latent episomal DNA

AutorJäger, Wiebke; Santag, Susann; Weidner-Glunde, Magdalena; Gellermann, Eva; Kati, Semra; Pietrek, Marcel; Viejo-Borbolla, Abel ; Schulz, Thomas F.
Fecha de publicación2012
EditorAmerican Society for Microbiology
CitaciónJournal of Virology 86 (12): 6745- 6757 (2012)
ResumenKaposi's sarcoma herpesvirus (KSHV) belongs to the gamma-2 Herpesviridae and is associated with three neoplastic disorders: Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castleman's disease (MCD). The viral latency-associated nuclear antigen 1 (LANA) is expressed in all latently KSHV-infected cells and is involved in viral latent replication and maintenance of the viral genome. We show that LANA interacts with the ubiquitin-specific protease USP7 through its N-terminal TRAF (tumor necrosis factor [TNF] receptor-associated factor) domain. This interaction involves a short sequence (amino acids [aa] 971 to 986) within the C-terminal domain of LANA with strong similarities to the USP7 binding site of the Epstein-Barr virus (EBV) EBNA-1 protein. A LANA mutant with a deletion of the identified USP7 binding site showed an enhanced ability to replicate a plasmid containing the KSHV latent origin of replication but was comparable to the wild-type LANA (LANA WT) with regard to the regulation of viral and cellular promoters. Furthermore, the LANA homologues of two other gamma-2 herpesviruses, MHV68 and RRV, also recruit USP7. Our findings suggest that recruitment of USP7 to LANA could play a role in the regulation of viral latent replication. The recruitment of USP7, and its role in herpesvirus latent replication, previously described for the latent EBNA-1 protein of the gamma-1 herpesvirus (lymphocryptovirus) EBV (M. N. Holowaty et al., J. Biol. Chem. 278:29987-29994, 2003), may thereby be a conserved feature among gammaherpesvirus latent origin binding proteins.
URIhttp://hdl.handle.net/10261/115028
DOI10.1128/JVI.06840-11
Identificadoresdoi: 10.1128/JVI.06840-11
issn: 0022-538X
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