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D'Arienzo, V.* ; Magri, A.* ; Harris, J.M.* ; Wing, P.A.C.* ; Ko, C. ; Rubio, C.O.* ; Revill, P.A.* ; Protzer, U. ; Balfe, P.* ; McKeating, J.A.*

A PCR assay to quantify patterns of HBV transcription.

J. Gen. Virol. 102, DOI: 10.1099/jgv.0.001373 (2019)
Verlagsversion DOI
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Hepatitis B virus (HBV) is the prototype member of the family Hepadnaviridae and replicates via episomal copies of a covalently closed circular DNA (cccDNA) genome of approximately 3.2 kb. The chromatinization of this small viral genome, with overlapping open reading frames and regulatory elements, suggests an important role for epigenetic pathways to regulate HBV transcription. However, the host pathways that regulate HBV transcription and the temporal nature of promoter usage in infected cells are not well understood, in part due to the compact genome structure and overlapping open reading frames. To address this we developed a simple and cost-effective PCR assay to quantify the major viral RNAs and validated this technique using current state-of-art de novo HBV infection model systems. Our PCR method is three orders of magnitude more sensitive than Northern blot and requires relatively small amounts of starting material, making this an attractive tool for assessing HBV transcription.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Hepatitis B Virus ; Rna ; Transcription
ISSN (print) / ISBN 0022-1317
e-ISSN 1465-2099
Quellenangaben Band: 102, Heft: 3 Seiten: , Artikelnummer: , Supplement: ,
Verlag Society for General Microbiology
Verlagsort Charles Darwin House, 12 Roger St, London Wc1n 2ju, Erks, England
Begutachtungsstatus Peer reviewed
Förderungen Wellcome Trust
EU 2020 Research and Innovation Programme Consortia HEP-CAR