Author
Listed:
- Adam W. Whisnant
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7)
- Christopher S. Jürges
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7)
- Thomas Hennig
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7)
- Emanuel Wyler
(Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine)
- Bhupesh Prusty
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7)
- Andrzej J. Rutkowski
(Department of Medicine, University of Cambridge, Box 157, Addenbrookes Hospital)
- Anne L’hernault
(Department of Medicine, University of Cambridge, Box 157, Addenbrookes Hospital)
- Lara Djakovic
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7)
- Margarete Göbel
(Julius-Maximilians-University Würzburg)
- Kristina Döring
(Julius-Maximilians-University Würzburg)
- Jennifer Menegatti
(Saarland University Medical School)
- Robin Antrobus
(University of Cambridge)
- Nicholas J. Matheson
(University of Cambridge)
- Florian W. H. Künzig
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7)
- Guido Mastrobuoni
(Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine)
- Chris Bielow
(Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine)
- Stefan Kempa
(Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine)
- Chunguang Liang
(Julius-Maximilians-University Würzburg)
- Thomas Dandekar
(Julius-Maximilians-University Würzburg)
- Ralf Zimmer
(Ludwig-Maximilians-Universität München)
- Markus Landthaler
(Berlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine)
- Friedrich Grässer
(Saarland University Medical School)
- Paul J. Lehner
(University of Cambridge)
- Caroline C. Friedel
(Ludwig-Maximilians-Universität München)
- Florian Erhard
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7)
- Lars Dölken
(Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, Versbacher Straße 7
Department of Medicine, University of Cambridge, Box 157, Addenbrookes Hospital
Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz-Center for Infection Research (HZI))
Abstract
The predicted 80 open reading frames (ORFs) of herpes simplex virus 1 (HSV-1) have been intensively studied for decades. Here, we unravel the complete viral transcriptome and translatome during lytic infection with base-pair resolution by computational integration of multi-omics data. We identify a total of 201 transcripts and 284 ORFs including all known and 46 novel large ORFs. This includes a so far unknown ORF in the locus deleted in the FDA-approved oncolytic virus Imlygic. Multiple transcript isoforms expressed from individual gene loci explain translation of the vast majority of ORFs as well as N-terminal extensions (NTEs) and truncations. We show that NTEs with non-canonical start codons govern the subcellular protein localization and packaging of key viral regulators and structural proteins. We extend the current nomenclature to include all viral gene products and provide a genome browser that visualizes all the obtained data from whole genome to single-nucleotide resolution.
Suggested Citation
Adam W. Whisnant & Christopher S. Jürges & Thomas Hennig & Emanuel Wyler & Bhupesh Prusty & Andrzej J. Rutkowski & Anne L’hernault & Lara Djakovic & Margarete Göbel & Kristina Döring & Jennifer Menega, 2020.
"Integrative functional genomics decodes herpes simplex virus 1,"
Nature Communications, Nature, vol. 11(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-15992-5
DOI: 10.1038/s41467-020-15992-5
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