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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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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 |
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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 |
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