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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
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.
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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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