| Literature DB >> 32315601 |
Rui Guo1, Chang Jiang1, Yuchen Zhang2, Apurva Govande3, Stephen J Trudeau1, Fang Chen4, Christopher J Fry4, Rishi Puri5, Emma Wolinsky1, Molly Schineller1, Thomas C Frost3, Makda Gebre3, Bo Zhao6, Lisa Giulino-Roth7, John G Doench8, Mingxiang Teng9, Benjamin E Gewurz10.
Abstract
Epstein-Barr virus (EBV) is associated with multiple human malignancies. To evade immune detection, EBV switches between latent and lytic programs. How viral latency is maintained in tumors or in memory B cells, the reservoir for lifelong EBV infection, remains incompletely understood. To gain insights, we performed a human genome-wide CRISPR/Cas9 screen in Burkitt lymphoma B cells. Our analyses identified a network of host factors that repress lytic reactivation, centered on the transcription factor MYC, including cohesins, FACT, STAGA, and Mediator. Depletion of MYC or factors important for MYC expression reactivated the lytic cycle, including in Burkitt xenografts. MYC bound the EBV genome origin of lytic replication and suppressed its looping to the lytic cycle initiator BZLF1 promoter. Notably, MYC abundance decreases with plasma cell differentiation, a key lytic reactivation trigger. Our results suggest that EBV senses MYC abundance as a readout of B cell state and highlights Burkitt latency reversal therapeutic targets.Entities:
Keywords: DNA looping; MYC; herpesvirus; latency reversal; lytic reactivation; tumor virus
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Year: 2020 PMID: 32315601 PMCID: PMC7245572 DOI: 10.1016/j.molcel.2020.03.025
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970