Unheeded SARS-CoV-2 proteins? A deep look into negative-sense RNA
Martin BartasiD, Adriana VolnáiD, Christopher A. BeaudoiniD, Ebbe Toftgaard PoulseniD, Jiří ČerveňiD, Václav BrázdaiD, Vladimı́r ŠpundaiD, Tom L. BlundelliD, Petr PečínkaiD
Abstract
SARS-CoV-2 is a novel positive-sense single-stranded RNA virus from the Coronaviridae family (genus Betacoronavirus), which has been established as causing the COVID-19 pandemic. The genome of SARS-CoV-2 is one of the largest among known RNA viruses, comprising of at least 26 known protein-coding loci. Studies thus far have outlined the coding capacity of the positive-sense strand of the SARS-CoV-2 genome, which can be used directly for protein translation. However, it has been recently shown that transcribed negative-sense viral RNA intermediates that arise during viral genome replication from positive-sense viruses can also code for proteins. No studies have yet explored the potential for negative-sense SARS-CoV-2 RNA intermediates to contain protein coding-loci. Thus, using sequence and structure-based bioinformatics methodologies, we have investigated the presence and validity of putative negative-sense ORFs (nsORFs) in the SARS-CoV-2 genome. Nine nsORFs were discovered to contain strong eukaryotic translation initiation signals and high codon adaptability scores, and several of the nsORFs were predicted to interact with RNA-binding proteins. Evolutionary conservation analyses indicated that some of the nsORFs are deeply conserved among related coronaviruses. Three-dimensional protein modelling revealed the presence of higher order folding among all putative SARS-CoV-2 nsORFs, and subsequent structural mimicry analyses suggest similarity of the nsORFs to DNA/RNA-binding proteins and proteins involved in immune signaling pathways. Altogether, these results suggest the potential existence of still undescribed SARS-CoV-2 proteins, which may play an important role in the viral lifecycle and COVID-19 pathogenesis. Contactpetr.pecinka@osu.cz; tlb20@cam.ac.uk
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 25
- FWCI
- 2.68
- Field percentile
- top 8%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Comprehensive in-vivo secondary structure of SARS-CoV-2 genome reveals novel regulatory motifs and mechanisms
Nicholas C Huston, Han Wan, … Anna Marie Pyle·Molecular CellPeer-reviewed·Feb 1, 2021
- Discovery and functional interrogation of SARS-CoV-2 protein-RNA interactions
Gene Wei-Ming Yeo, Joy S. Xiang, … Sandra Lawrynowicz Leibel·bioRxiv·Feb 21, 2022
- In vivo structural characterization of the whole SARS-CoV-2 RNA genome identifies host cell target proteins vulnerable to re-purposed drugs
Lei Sun, Pan Li, … Qiangfeng Cliff Zhang·CellPeer-reviewed·Apr 1, 2021
- The coding capacity of SARS-CoV-2
Y. Finkel, O. Mizrahi, … N. Stern-Ginossar·NaturePeer-reviewed·Sep 9, 2020
- Mapping the host protein interactome of non-coding regions in SARS-CoV-2 genome
Liuyiqi Jiang, Mu Xiao, … Xin‐Hua Feng·bioRxiv·Jun 19, 2021
- The proximal proteome of 17 SARS-CoV-2 proteins links to disrupted antiviral signaling and host translation
J. Meyers, M. Ramanathan, … P. Khavari·bioRxiv·Feb 23, 2021