cdc2/cyclin B1-dependent phosphorylation of EBNA2 at Ser243 regulates its function in mitosis.

Abstract:

:Epstein-Barr virus (EBV) nuclear antigen 2 (EBNA2) transactivates EBV genes in latently infected B cells. We have shown that mitotic hyperphosphorylation of EBNA2 suppresses its ability to transactivate the latent membrane protein 1 (LMP1) promoter. In this follow-up study, we identify EBNA2 Ser243 as a phosphorylation site for mitotic cdc2/cyclin B1 kinase. Mutation at Ser243, which mimics constitutive phosphorylation of the protein, decreases endogenous levels of both LMP1 and EBNA2. Moreover, mutation at Ser243 reduces the ability of EBNA2 to transactivate Cp, the promoter for all six EBV EBNA genes. Our data implicate EBNA2 Ser243 as a cdc2/cyclin B1 site of phosphorylation important for EBNA2's cotranscriptional function in mitosis.

journal_name

J Virol

journal_title

Journal of virology

authors

Yue W,Shackelford J,Pagano JS

doi

10.1128/JVI.80.4.2045-2050.2006

subject

Has Abstract

pub_date

2006-02-01 00:00:00

pages

2045-50

issue

4

eissn

0022-538X

issn

1098-5514

pii

80/4/2045

journal_volume

80

pub_type

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