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In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome

AIM: The aim of this study was to computationally predict conserved RNA sequences and structures known as cis-acting RNA elements (CREs) in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome. MATERIALS & METHODS: Bioinformatics tools were used to analyze and predict CREs by...

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Autor principal: Alhatlani, Bader Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507811/
https://www.ncbi.nlm.nih.gov/pubmed/33005212
http://dx.doi.org/10.2217/fvl-2020-0163
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author Alhatlani, Bader Y
author_facet Alhatlani, Bader Y
author_sort Alhatlani, Bader Y
collection PubMed
description AIM: The aim of this study was to computationally predict conserved RNA sequences and structures known as cis-acting RNA elements (CREs) in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome. MATERIALS & METHODS: Bioinformatics tools were used to analyze and predict CREs by obtaining viral sequences from available databases. RESULTS: Computational analysis revealed the presence of RNA stem-loop structures within the 3′ end of the ORF1ab region analogous to previously identified SARS-CoV genomic packaging signals. Alignment-based RNA secondary structure predictions of the 5′ end of the SARS-CoV-2 genome also identified conserved CREs. CONCLUSION: These CREs may be potential vaccine and/or antiviral therapeutic targets; however, further studies are warranted to confirm their roles in the SARS-CoV-2 life cycle.
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spelling pubmed-75078112020-09-29 In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome Alhatlani, Bader Y Future Virol Short Communication AIM: The aim of this study was to computationally predict conserved RNA sequences and structures known as cis-acting RNA elements (CREs) in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome. MATERIALS & METHODS: Bioinformatics tools were used to analyze and predict CREs by obtaining viral sequences from available databases. RESULTS: Computational analysis revealed the presence of RNA stem-loop structures within the 3′ end of the ORF1ab region analogous to previously identified SARS-CoV genomic packaging signals. Alignment-based RNA secondary structure predictions of the 5′ end of the SARS-CoV-2 genome also identified conserved CREs. CONCLUSION: These CREs may be potential vaccine and/or antiviral therapeutic targets; however, further studies are warranted to confirm their roles in the SARS-CoV-2 life cycle. Future Medicine Ltd 2020-07-29 2020-07 /pmc/articles/PMC7507811/ /pubmed/33005212 http://dx.doi.org/10.2217/fvl-2020-0163 Text en © 2020 Future Medicine Ltd This work is licensed under the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Short Communication
Alhatlani, Bader Y
In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome
title In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome
title_full In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome
title_fullStr In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome
title_full_unstemmed In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome
title_short In silico identification of conserved cis-acting RNA elements in the SARS-CoV-2 genome
title_sort in silico identification of conserved cis-acting rna elements in the sars-cov-2 genome
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507811/
https://www.ncbi.nlm.nih.gov/pubmed/33005212
http://dx.doi.org/10.2217/fvl-2020-0163
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