Bromodomain proteins regulate human cytomegalovirus latency and reactivation allowing epigenetic therapeutic intervention
نویسندگان
چکیده
Significance Human cytomegalovirus (HCMV) reactivation is a major cause of posttransplant morbidity/mortality. One approach toward reducing this purging the transplant donor and/or recipient latently infected cells prior to stem-cell or organ harvest/engraftment. Our findings show involvement host bromodomain (BRD) proteins in regulation HCMV latency and reactivation. Bromodomain extra-terminal inhibitor (I-BET) treatment causes lytic gene expression by release transcription activator P-TEFb (CDK9/CycT1) from BRD4-associated repressive complexes, with subsequent recruitment via superelongation complex (SEC). This results immune targeting T cell-mediated killing these otherwise provides therapeutic “shock kill” strategy that could reduce HCMV-mediated disease setting.
منابع مشابه
Epigenetic Control of Cytomegalovirus Latency and Reactivation
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ژورنال
عنوان ژورنال: Proceedings of the National Academy of Sciences of the United States of America
سال: 2021
ISSN: ['1091-6490', '0027-8424']
DOI: https://doi.org/10.1073/pnas.2023025118