Abstract
While all herpesviruses can switch between lytic and latent life cycle, which are both driven by specific transcription programs, a unique feature of latent EBV infection is the expression of several distinct and well-defined viral latent transcription programs called latency I, II, and III. Growth transformation of B-cells by EBV in vitro is based on the concerted action of Epstein-Barr virus nuclear antigens (EBNAs) and latent membrane proteins(LMPs). EBV growth-transformed B-cells express a viral transcriptional program, termed latency III, which is characterized by the coexpression of EBNA2 and EBNA-LP with EBNA1, EBNA3A, -3B, and -3C as well as LMP1, LMP2A, and LMP2B. The focus of this review will be to discuss the current understanding of how two of these proteins, EBNA2 and EBNA-LP, contribute to EBV-mediated B-cell growth transformation.
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Notes
- 1.
In this review, we will refer to the primary structure of EBNA2 using the Swiss-Prot data entry of EBV laboratory strain 95-8:P12978.
Abbreviations
- CBF1:
-
C-promoter binding factor
- EBNA:
-
Epstein-Barr virus nuclear antigen
- EBNA-LP:
-
Epstein-Barr virus leader protein
- LMP:
-
Latent membrane protein
- LCL:
-
Lymphoblastoid cell line
- LCV:
-
Lymphocryptovirus
- TAD:
-
Transactivation domain
- PML-NB:
-
Promyelocytic leukemia nuclear body
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Acknowledgments
The research of BK is supported by the HELENA graduate school of the Helmholtz Center Munich and the Deutsche Krebshilfe (grant 109258). PDL is supported by NIH grant 5R01AI080681.
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Kempkes, B., Ling, P.D. (2015). EBNA2 and Its Coactivator EBNA-LP. In: Münz, C. (eds) Epstein Barr Virus Volume 2. Current Topics in Microbiology and Immunology, vol 391. Springer, Cham. https://doi.org/10.1007/978-3-319-22834-1_2
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