Cargando…

Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging

Viruses must efficiently and specifically package their genomes while excluding cellular nucleic acids and viral sub-genomic fragments. Some viruses use specific packaging signals, which are conserved sequence/structure motifs present only in the full-length genome. Recent work has shown that viral...

Descripción completa

Detalles Bibliográficos
Autores principales: Seim, Ian, Roden, Christine A., Gladfelter, Amy S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7805453/
https://www.ncbi.nlm.nih.gov/pubmed/33442696
http://dx.doi.org/10.1101/2021.01.06.425605
_version_ 1783636313838190592
author Seim, Ian
Roden, Christine A.
Gladfelter, Amy S.
author_facet Seim, Ian
Roden, Christine A.
Gladfelter, Amy S.
author_sort Seim, Ian
collection PubMed
description Viruses must efficiently and specifically package their genomes while excluding cellular nucleic acids and viral sub-genomic fragments. Some viruses use specific packaging signals, which are conserved sequence/structure motifs present only in the full-length genome. Recent work has shown that viral proteins important for packaging can undergo liquid-liquid phase separation (LLPS), where one or two viral nucleic acid binding proteins condense with the genome. The compositional simplicity of viral components lends itself well to theoretical modeling compared to more complex cellular organelles. Viral LLPS can be limited to one or two viral proteins and a single genome that is enriched in LLPS-promoting features. In our previous study, we observed that LLPS-promoting sequences of SARS-CoV-2 are located at the 5′ and 3′ ends of the genome, whereas the middle of the genome is predicted to consist mostly of solubilizing elements. Is this arrangement sufficient to drive single genome packaging, genome compaction, and genome cyclization? We addressed these questions using a coarse-grained polymer model, LASSI, to study the LLPS of nucleocapsid protein with RNA sequences that either promote LLPS or solubilization. With respect to genome cyclization, we find the most optimal arrangement restricts LLPS-promoting elements to the 5′ and 3′ ends of the genome, consistent with the native spatial patterning. Genome compaction is enhanced by clustered LLPS-promoting binding sites, while single genome packaging is most efficient when binding sites are distributed throughout the genome. These results suggest that many and variably positioned LLPS-promoting signals can support packaging in the absence of a singular packaging signal which argues against necessity of such a feature. We hypothesize that this model should be generalizable to multiple viruses as well as cellular organelles like paraspeckles, which enrich specific, long RNA sequences in a defined arrangement.
format Online
Article
Text
id pubmed-7805453
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-78054532021-01-14 Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging Seim, Ian Roden, Christine A. Gladfelter, Amy S. bioRxiv Article Viruses must efficiently and specifically package their genomes while excluding cellular nucleic acids and viral sub-genomic fragments. Some viruses use specific packaging signals, which are conserved sequence/structure motifs present only in the full-length genome. Recent work has shown that viral proteins important for packaging can undergo liquid-liquid phase separation (LLPS), where one or two viral nucleic acid binding proteins condense with the genome. The compositional simplicity of viral components lends itself well to theoretical modeling compared to more complex cellular organelles. Viral LLPS can be limited to one or two viral proteins and a single genome that is enriched in LLPS-promoting features. In our previous study, we observed that LLPS-promoting sequences of SARS-CoV-2 are located at the 5′ and 3′ ends of the genome, whereas the middle of the genome is predicted to consist mostly of solubilizing elements. Is this arrangement sufficient to drive single genome packaging, genome compaction, and genome cyclization? We addressed these questions using a coarse-grained polymer model, LASSI, to study the LLPS of nucleocapsid protein with RNA sequences that either promote LLPS or solubilization. With respect to genome cyclization, we find the most optimal arrangement restricts LLPS-promoting elements to the 5′ and 3′ ends of the genome, consistent with the native spatial patterning. Genome compaction is enhanced by clustered LLPS-promoting binding sites, while single genome packaging is most efficient when binding sites are distributed throughout the genome. These results suggest that many and variably positioned LLPS-promoting signals can support packaging in the absence of a singular packaging signal which argues against necessity of such a feature. We hypothesize that this model should be generalizable to multiple viruses as well as cellular organelles like paraspeckles, which enrich specific, long RNA sequences in a defined arrangement. Cold Spring Harbor Laboratory 2021-04-26 /pmc/articles/PMC7805453/ /pubmed/33442696 http://dx.doi.org/10.1101/2021.01.06.425605 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Seim, Ian
Roden, Christine A.
Gladfelter, Amy S.
Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging
title Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging
title_full Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging
title_fullStr Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging
title_full_unstemmed Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging
title_short Role of spatial patterning of N-protein interactions in SARS-CoV-2 genome packaging
title_sort role of spatial patterning of n-protein interactions in sars-cov-2 genome packaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7805453/
https://www.ncbi.nlm.nih.gov/pubmed/33442696
http://dx.doi.org/10.1101/2021.01.06.425605
work_keys_str_mv AT seimian roleofspatialpatterningofnproteininteractionsinsarscov2genomepackaging
AT rodenchristinea roleofspatialpatterningofnproteininteractionsinsarscov2genomepackaging
AT gladfelteramys roleofspatialpatterningofnproteininteractionsinsarscov2genomepackaging