Imperial College London

Dr Rob White

Faculty of MedicineDepartment of Medicine

Non-Clinical Lecturer in Virology
 
 
 
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Contact

 

+44 (0)20 7594 1124robert.e.white Website

 
 
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Location

 

308Norfolk PlaceSt Mary's Campus

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Summary

 

Publications

Citation

BibTex format

@article{Styles:2018:10.3390/pathogens7010031,
author = {Styles, CT and Paschos, K and White, R and Farrell, PJ},
doi = {10.3390/pathogens7010031},
journal = {Pathogens},
title = {The cooperative functions of the EBNA3 Proteins are central to EBV persistence and latency},
url = {http://dx.doi.org/10.3390/pathogens7010031},
volume = {31},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The Epstein–Barr nuclear antigen 3 (EBNA3) family of proteins, comprising EBNA3A, EBNA3B, and EBNA3C, play pivotal roles in the asymptomatic persistence and life-long latency of Epstein–Barr virus (EBV) in the worldwide human population. EBNA3-mediated transcriptional reprogramming of numerous host cell genes promotes in vitro B cell transformation and EBV persistence in vivo. Despite structural and sequence similarities, and evidence of substantial cooperative activity between the EBNA3 proteins, they perform quite different, often opposing functions. Both EBNA3A and EBNA3C are involved in the repression of important tumour suppressive pathways and are considered oncogenic. In contrast, EBNA3B exhibits tumour suppressive functions. This review focuses on how the EBNA3 proteins achieve the delicate balance required to support EBV persistence and latency, with emphasis on the contribution of the Allday laboratory to the field of EBNA3 biology.
AU - Styles,CT
AU - Paschos,K
AU - White,R
AU - Farrell,PJ
DO - 10.3390/pathogens7010031
PY - 2018///
SN - 2076-0817
TI - The cooperative functions of the EBNA3 Proteins are central to EBV persistence and latency
T2 - Pathogens
UR - http://dx.doi.org/10.3390/pathogens7010031
UR - http://hdl.handle.net/10044/1/58388
VL - 31
ER -