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Hammerschmidt, W.

The epigenetic life cycle of epstein–barr virus.

Curr. Top. Microbiol. Immunol. 390, 103-117 (2015)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Ever since the discovery of Epstein–Barr virus (EBV) more than 50 years ago, this virus has been studied for its capacity to readily establish a latent infection, which is the prominent hallmark of this member of the herpesvirus family. EBV has become an important model for many aspects of herpesviral latency, but the molecular steps and mechanisms that lead to and promote viral latency have only emerged recently. It now appears that the virus exploits diverse facets of epigenetic gene regulation in the cellular host to establish a latent infection. Most viral genes are transcriptionally repressed, and viral chromatin is densely compacted during EBV’s latent phase, but latent infection is not a dead end. In order to escape from this phase, epigenetic silencing must be reverted efficiently and quickly. It appears that EBV has perfected a clever strategy to overcome transcriptional repression of its many lytic genes to initiate virus de novo synthesis within a few hours after induction of its lytic cycle. This review tries to summarize the known molecular mechanisms, the current models, concepts, and ideas underlying this viral strategy. This review also attempts to identify and address gaps in our current understanding of EBV’s epigenetic mechanisms within the infected cellular host.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Dna Methylation ; Epigenetics ; Pioneer Factor ; Reprogramming ; Transcription; B-cell Transformation; Viral Genome; Epithelial-cells; Dna-replication; Initial-stages; Gene Promoter; Lytic Switch; Infection; Latent; Methylation
ISSN (print) / ISBN 0070-217x
e-ISSN 0070-217X
Konferenztitel Epstein Barr Virus Volume 1 : One Herpes Virus: Many Diseases
Zeitschrift Current Topics in Microbiology and Immunology
Quellenangaben Band: 390, Heft: , Seiten: 103-117 Artikelnummer: , Supplement: ,
Verlag Springer
Verlagsort Berlin ; Heidelberg [u.a.]
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Research Unit Gene Vector (AGV)