Epstein-Barr virus LMP1 blocks p(16INK4a)-RB pathway by promoting nuclear export of E2F4/5
Web of Science
AuthorOhtani, N; Brennan, P; Gaubatz, S; Sanij, E; Hertzog, P; Wolvetang, E; Ghysdael, J; Rowe, M; Hara, E
Source TitleThe Journal of Cell Biology
PublisherROCKEFELLER UNIV PRESS
AffiliationSir Peter MacCallum Department of Oncology
Microbiology and Immunology
Document TypeJournal Article
CitationsOhtani, N., Brennan, P., Gaubatz, S., Sanij, E., Hertzog, P., Wolvetang, E., Ghysdael, J., Rowe, M. & Hara, E. (2003). Epstein-Barr virus LMP1 blocks p(16INK4a)-RB pathway by promoting nuclear export of E2F4/5. JOURNAL OF CELL BIOLOGY, 162 (2), pp.173-183. https://doi.org/10.1083/jcb.200302085.
Access StatusOpen Access
The p16INK4a-RB pathway plays a critical role in preventing inappropriate cell proliferation and is often targeted by viral oncoproteins during immortalization. Latent membrane protein 1 (LMP1) of Epstein-Barr virus (EBV) is often present in EBV-associated proliferative diseases and is critical for the immortalizing and transforming activity of EBV. Unlike other DNA tumor virus oncoproteins, which possess immortalizing activity, LMP1 does not bind to retinoblastoma tumor suppressor protein, but instead blocks the expression of p16INK4a tumor suppressor gene. However, it has been unclear how LMP1 represses the p16INK4a gene expression. Here, we report that LMP1 promotes the CRM1-dependent nuclear export of Ets2, which is an important transcription factor for p16INK4a gene expression, thereby reducing the level of p16INK4a expression. We further demonstrate that LMP1 also blocks the function of E2F4 and E2F5 (E2F4/5) transcription factors through promoting their nuclear export in a CRM1-dependent manner. As E2F4/5 are essential downstream mediators for a p16INK4a-induced cell cycle arrest, these results indicate that the action of LMP1 on nuclear export has two effects on the p16INK4a-RB pathway: (1) repression of p16INK4a expression and (2) blocking the downstream mediator of the p16INK4a-RB pathway. These results reveal a novel activity of LMP1 and increase an understanding of how viral oncoproteins perturb the p16INK4a-RB pathway.
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