dc.contributor.author
Saviola, Anthony J.
dc.contributor.author
Zimmermann, Cosima
dc.contributor.author
Mariani P., Michael
dc.contributor.author
Signorelli, Sylvia A.
dc.contributor.author
Gerrard, Diana L.
dc.contributor.author
Boyd, Joseph R.
dc.contributor.author
Wight, Darren J.
dc.contributor.author
Morissette, Guillaume
dc.contributor.author
Gravel, Annie
dc.contributor.author
Dubuc, Isabelle
dc.contributor.author
Flamand, Louis
dc.contributor.author
Kaufer, Benedikt B.
dc.contributor.author
Frietze, Seth
dc.date.accessioned
2019-07-15T09:17:06Z
dc.date.available
2019-07-15T09:17:06Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/25059
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-2814
dc.description.abstract
Human herpesvirus-6A (HHV-6A) and 6B (HHV-6B) are two closely related betaherpesviruses that are associated with various diseases including seizures and encephalitis. The HHV-6A/B genomes have been shown to be present in an integrated state in the telomeres of latently infected cells. In addition, integration of HHV-6A/B in germ cells has resulted in individuals harboring this inherited chromosomally integrated HHV-6A/B (iciHHV-6) in every cell of their body. Until now, the viral transcriptome and the epigenetic modifications that contribute to the silencing of the integrated virus genome remain elusive. In the current study, we used a patient-derived iciHHV-6A cell line to assess the global viral gene expression profile by RNA-seq, and the chromatin profiles by MNase-seq and ChIP-seq analyses. In addition, we investigated an in vitro generated cell line (293-HHV-6A) that expresses GFP upon the addition of agents commonly used to induce herpesvirus reactivation such as TPA. No viral gene expression including miRNAs was detected from the HHV-6A genomes, indicating that the integrated virus is transcriptionally silent. Intriguingly, upon stimulation of the 293-HHV-6A cell line with TPA, only foreign promoters in the virus genome were activated, while all HHV-6A promoters remained completely silenced. The transcriptional silencing of latent HHV-6A was further supported by MNase-seq results, which demonstrate that the latent viral genome resides in a highly condensed nucleosome-associated state. We further explored the enrichment profiles of histone modifications via ChIP-seq analysis. Our results indicated that the HHV-6 genome is modestly enriched with the repressive histone marks H3K9me3/H3K27me3 and does not possess the active histone modifications H3K27ac/H3K4me3. Overall, these results indicate that HHV-6 genomes reside in a condensed chromatin state, providing insight into the epigenetic mechanisms associated with the silencing of the integrated HHV-6A genome.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::579 Mikroorganismen, Pilze, Algen
dc.title
Chromatin Profiles of Chromosomally Integrated Human Herpesvirus-6A
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
1408
dcterms.bibliographicCitation.doi
10.3389/fmicb.2019.01408
dcterms.bibliographicCitation.journaltitle
Frontiers in Microbiology
dcterms.bibliographicCitation.volume
10
dcterms.bibliographicCitation.url
https://doi.org/10.3389/fmicb.2019.01408
refubium.affiliation
Veterinärmedizin
refubium.affiliation.other
Institut für Virologie
refubium.note.author
Die Publikation wurde aus Open Access Publikationsgeldern der Freien Universität Berlin und der DFG gefördert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1664-302X