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pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread
The herpes simplex virus (HSV)-1 protein pUL21 is essential for efficient virus replication and dissemination. While pUL21 has been shown to promote multiple steps of virus assembly and spread, the molecular basis of its function remained unclear. Here we identify that pUL21 is a virus-encoded adapt...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389370/ https://www.ncbi.nlm.nih.gov/pubmed/34398933 http://dx.doi.org/10.1371/journal.ppat.1009824 |
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author | Benedyk, Tomasz H. Muenzner, Julia Connor, Viv Han, Yue Brown, Katherine Wijesinghe, Kaveesha J. Zhuang, Yunhui Colaco, Susanna Stoll, Guido A. Tutt, Owen S. Svobodova, Stanislava Svergun, Dmitri I. Bryant, Neil A. Deane, Janet E. Firth, Andrew E. Jeffries, Cy M. Crump, Colin M. Graham, Stephen C. |
author_facet | Benedyk, Tomasz H. Muenzner, Julia Connor, Viv Han, Yue Brown, Katherine Wijesinghe, Kaveesha J. Zhuang, Yunhui Colaco, Susanna Stoll, Guido A. Tutt, Owen S. Svobodova, Stanislava Svergun, Dmitri I. Bryant, Neil A. Deane, Janet E. Firth, Andrew E. Jeffries, Cy M. Crump, Colin M. Graham, Stephen C. |
author_sort | Benedyk, Tomasz H. |
collection | PubMed |
description | The herpes simplex virus (HSV)-1 protein pUL21 is essential for efficient virus replication and dissemination. While pUL21 has been shown to promote multiple steps of virus assembly and spread, the molecular basis of its function remained unclear. Here we identify that pUL21 is a virus-encoded adaptor of protein phosphatase 1 (PP1). pUL21 directs the dephosphorylation of cellular and virus proteins, including components of the viral nuclear egress complex, and we define a conserved non-canonical linear motif in pUL21 that is essential for PP1 recruitment. In vitro evolution experiments reveal that pUL21 antagonises the activity of the virus-encoded kinase pUS3, with growth and spread of pUL21 PP1-binding mutant viruses being restored in adapted strains where pUS3 activity is disrupted. This study shows that virus-directed phosphatase activity is essential for efficient herpesvirus assembly and spread, highlighting the fine balance between kinase and phosphatase activity required for optimal virus replication. |
format | Online Article Text |
id | pubmed-8389370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83893702021-08-27 pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread Benedyk, Tomasz H. Muenzner, Julia Connor, Viv Han, Yue Brown, Katherine Wijesinghe, Kaveesha J. Zhuang, Yunhui Colaco, Susanna Stoll, Guido A. Tutt, Owen S. Svobodova, Stanislava Svergun, Dmitri I. Bryant, Neil A. Deane, Janet E. Firth, Andrew E. Jeffries, Cy M. Crump, Colin M. Graham, Stephen C. PLoS Pathog Research Article The herpes simplex virus (HSV)-1 protein pUL21 is essential for efficient virus replication and dissemination. While pUL21 has been shown to promote multiple steps of virus assembly and spread, the molecular basis of its function remained unclear. Here we identify that pUL21 is a virus-encoded adaptor of protein phosphatase 1 (PP1). pUL21 directs the dephosphorylation of cellular and virus proteins, including components of the viral nuclear egress complex, and we define a conserved non-canonical linear motif in pUL21 that is essential for PP1 recruitment. In vitro evolution experiments reveal that pUL21 antagonises the activity of the virus-encoded kinase pUS3, with growth and spread of pUL21 PP1-binding mutant viruses being restored in adapted strains where pUS3 activity is disrupted. This study shows that virus-directed phosphatase activity is essential for efficient herpesvirus assembly and spread, highlighting the fine balance between kinase and phosphatase activity required for optimal virus replication. Public Library of Science 2021-08-16 /pmc/articles/PMC8389370/ /pubmed/34398933 http://dx.doi.org/10.1371/journal.ppat.1009824 Text en © 2021 Benedyk et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Benedyk, Tomasz H. Muenzner, Julia Connor, Viv Han, Yue Brown, Katherine Wijesinghe, Kaveesha J. Zhuang, Yunhui Colaco, Susanna Stoll, Guido A. Tutt, Owen S. Svobodova, Stanislava Svergun, Dmitri I. Bryant, Neil A. Deane, Janet E. Firth, Andrew E. Jeffries, Cy M. Crump, Colin M. Graham, Stephen C. pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
title | pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
title_full | pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
title_fullStr | pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
title_full_unstemmed | pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
title_short | pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
title_sort | pul21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389370/ https://www.ncbi.nlm.nih.gov/pubmed/34398933 http://dx.doi.org/10.1371/journal.ppat.1009824 |
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