Transcription termination and readthrough in African swine fever virus.

African swine fever virus (ASFV) Oxford Nanopore RNA polymerase long-read sequencing transcription readthrough transcription termination transcriptomics

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2024
Historique:
received: 05 12 2023
accepted: 30 01 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: epublish

Résumé

African swine fever virus (ASFV) is a nucleocytoplasmic large DNA virus (NCLDV) that encodes its own host-like RNA polymerase (RNAP) and factors required to produce mature mRNA. The formation of accurate mRNA 3' ends by ASFV RNAP depends on transcription termination, likely enabled by a combination of sequence motifs and transcription factors, although these are poorly understood. The termination of any RNAP is rarely 100% efficient, and the transcriptional "readthrough" at terminators can generate long mRNAs which may interfere with the expression of downstream genes. ASFV transcriptome analyses reveal a landscape of heterogeneous mRNA 3' termini, likely a combination of Here, we report a rigorous analysis of full-length ASFV transcripts using long-read sequencing (LRS). We systematically compared transcription termination sites predicted from SRS 3' RNA-seq with 3' ends mapped by LRS during early and late infection. Using This indicates that ASFV mRNAs under the control of late gene promoters utilize different termination mechanisms and factors to early promoters and/or that cellular factors influence the viral transcriptome landscape differently during the late stages of infection.

Identifiants

pubmed: 38545109
doi: 10.3389/fimmu.2024.1350267
pmc: PMC10965686
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1350267

Informations de copyright

Copyright © 2024 Cackett, Sýkora, Portugal, Dulson, Dixon and Werner.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Gwenny Cackett (G)

Institute for Structural and Molecular Biology, University College London, London, United Kingdom.

Michal Sýkora (M)

Institute for Structural and Molecular Biology, University College London, London, United Kingdom.

Raquel Portugal (R)

Pirbright Institute, Pirbright, Surrey, United Kingdom.

Christopher Dulson (C)

Institute for Structural and Molecular Biology, University College London, London, United Kingdom.

Linda Dixon (L)

Pirbright Institute, Pirbright, Surrey, United Kingdom.

Finn Werner (F)

Institute for Structural and Molecular Biology, University College London, London, United Kingdom.

Classifications MeSH