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Please use this identifier to cite or link to this item: http://hdl.handle.net/1783.1/1324
Title: Elucidation of the c-Jun N-terminal kinase pathway mediated by epstein-barr virus-encoded latent membrane protein 1
Authors: Wan, Jun
Sun, Luguo
Mendoza, Jennifer Woo
Chui, Yiu Loon
Huang, Dolly P.
Chen, Zhijian J.
Suzuki, Nobutaka
Suzuki, Shinobu
Yeh, Wen-Chen
Akira, Shizuo
Matsumoto, Kunihiro
Liu, Zheng-gang
Wu, Zhenguo
Keywords: Epstein-Barr virus
EBV
LMP1
JNK
TNF
TAK1/TAB1
Issue Date: 2004
Citation: Molecular and cellular biology, v. 24, no. 1, Jan. 2004, p. 192-199
Abstract: Epstein-Barr virus (EBV) is associated with several human diseases including infectious mononucleosis and nasopharyngeal carcinoma. EBV-encoded latent membrane protein 1 (LMP1) is oncogenic and indispensable for cellular transformation caused by EBV. Expression of LMP1 in host cells constitutively activates both the c-Jun N-terminal kinase (JNK) and NF-κB pathways, which contributes to the oncogenic effect of LMP1. However, the underlying signaling mechanisms are not very well understood. Based mainly on overexpression studies with various dominant-negative constructs, LMP1 was generally thought to functionally mimic members of the tumor necrosis factor (TNF) receptor superfamily in signaling. In contrast to the prevailing paradigm, using embryonic fibroblasts from different knockout mice and the small interfering RNA technique, we find that the LMP1-mediated JNK pathway is distinct from those mediated by either TNF-α or interleukin-1. Moreover, we have further elucidated the LMP1-mediated JNK pathway by demonstrating that LMP1 selectively utilizes TNF receptor-associated factor 6, TAK1/TAB1, and c-Jun N-terminal kinase kinases 1 and 2 to activate JNK.
Rights: Copyright © American Society for Microbiology [Molecular and Cellular Biology, v. 24, no. 1, Jan. 2004, p. 192-199]
URI: http://hdl.handle.net/1783.1/1324
Appears in Collections:BICH Journal/Magazine Articles

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