Rotavirus Replication Factories Are Complex Ribonucleoprotein Condensates
Abstract RNA viruses induce formation of subcellular organelles that provide microenvironments conducive to their replication. Here we show that replication factories of rotaviruses represent protein-RNA condensates that are formed via liquid-liquid phase separation. We demonstrate that rotavirus proteins NSP5 and NSP2 undergo phase separation in vitro and form RNA-rich condensates in vivo that can be reversibly dissolved by aliphatic diols. During infection, these RNA-protein condensates became less dynamic and impervious to aliphatic diols, indicating a transition from a liquid to solid state. Some aspects of assembly of rotavirus replication factories mirror the formation of cytoplasmic ribonucleoprotein granules, while the selective enrichment of viral transcripts appears to be a unique feature of these condensates. Such complex RNA-protein condensates that underlie replication of RNA viruses represent an attractive target for developing novel therapeutic approaches..
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Preprint| Erscheinungsjahr: |
2021 |
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| Erschienen: |
2021 |
| Enthalten in: |
bioRxiv.org - (2021) vom: 15. Dez. Zur Gesamtaufnahme - year:2021 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Geiger, Florian [VerfasserIn] |
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| Links: |
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| doi: |
10.1101/2020.12.18.423429 |
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| PPN (Katalog-ID): |
XBI019598335 |
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| 520 | |a Abstract RNA viruses induce formation of subcellular organelles that provide microenvironments conducive to their replication. Here we show that replication factories of rotaviruses represent protein-RNA condensates that are formed via liquid-liquid phase separation. We demonstrate that rotavirus proteins NSP5 and NSP2 undergo phase separation in vitro and form RNA-rich condensates in vivo that can be reversibly dissolved by aliphatic diols. During infection, these RNA-protein condensates became less dynamic and impervious to aliphatic diols, indicating a transition from a liquid to solid state. Some aspects of assembly of rotavirus replication factories mirror the formation of cytoplasmic ribonucleoprotein granules, while the selective enrichment of viral transcripts appears to be a unique feature of these condensates. Such complex RNA-protein condensates that underlie replication of RNA viruses represent an attractive target for developing novel therapeutic approaches. | ||
| 700 | 1 | |a Papa, Guido |e verfasserin |4 aut | |
| 700 | 1 | |a Arter, William E. |e verfasserin |4 aut | |
| 700 | 1 | |a Acker, Julia |e verfasserin |4 aut | |
| 700 | 1 | |a Saar, Kadi L. |e verfasserin |4 aut | |
| 700 | 1 | |a Erkamp, Nadia |e verfasserin |4 aut | |
| 700 | 1 | |a Qi, Runzhang |e verfasserin |4 aut | |
| 700 | 1 | |a Bravo, Jack |e verfasserin |4 aut | |
| 700 | 1 | |a Strauss, Sebastian |e verfasserin |4 aut | |
| 700 | 1 | |a Krainer, Georg |e verfasserin |4 aut | |
| 700 | 1 | |a Burrone, Oscar R. |e verfasserin |4 aut | |
| 700 | 1 | |a Jungmann, Ralf |e verfasserin |4 aut | |
| 700 | 1 | |a Knowles, Tuomas P.J. |e verfasserin |4 aut | |
| 700 | 1 | |a Engelke, Hanna |e verfasserin |4 aut | |
| 700 | 1 | |a Borodavka, Alexander |e verfasserin |4 aut | |
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