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SAMHD1 … and Viral Ways around It
The SAM and HD domain-containing protein 1 (SAMHD1) is a dNTP triphosphohydrolase that plays a crucial role for a variety of different cellular functions. Besides balancing intracellular dNTP concentrations, facilitating DNA damage repair, and dampening excessive immune responses, SAMHD1 has been sh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999308/ https://www.ncbi.nlm.nih.gov/pubmed/33801276 http://dx.doi.org/10.3390/v13030395 |
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author | Deutschmann, Janina Gramberg, Thomas |
author_facet | Deutschmann, Janina Gramberg, Thomas |
author_sort | Deutschmann, Janina |
collection | PubMed |
description | The SAM and HD domain-containing protein 1 (SAMHD1) is a dNTP triphosphohydrolase that plays a crucial role for a variety of different cellular functions. Besides balancing intracellular dNTP concentrations, facilitating DNA damage repair, and dampening excessive immune responses, SAMHD1 has been shown to act as a major restriction factor against various virus species. In addition to its well-described activity against retroviruses such as HIV-1, SAMHD1 has been identified to reduce the infectivity of different DNA viruses such as the herpesviruses CMV and EBV, the poxvirus VACV, or the hepadnavirus HBV. While some viruses are efficiently restricted by SAMHD1, others have developed evasion mechanisms that antagonize the antiviral activity of SAMHD1. Within this review, we summarize the different cellular functions of SAMHD1 and highlight the countermeasures viruses have evolved to neutralize the restriction factor SAMHD1. |
format | Online Article Text |
id | pubmed-7999308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79993082021-03-28 SAMHD1 … and Viral Ways around It Deutschmann, Janina Gramberg, Thomas Viruses Review The SAM and HD domain-containing protein 1 (SAMHD1) is a dNTP triphosphohydrolase that plays a crucial role for a variety of different cellular functions. Besides balancing intracellular dNTP concentrations, facilitating DNA damage repair, and dampening excessive immune responses, SAMHD1 has been shown to act as a major restriction factor against various virus species. In addition to its well-described activity against retroviruses such as HIV-1, SAMHD1 has been identified to reduce the infectivity of different DNA viruses such as the herpesviruses CMV and EBV, the poxvirus VACV, or the hepadnavirus HBV. While some viruses are efficiently restricted by SAMHD1, others have developed evasion mechanisms that antagonize the antiviral activity of SAMHD1. Within this review, we summarize the different cellular functions of SAMHD1 and highlight the countermeasures viruses have evolved to neutralize the restriction factor SAMHD1. MDPI 2021-03-02 /pmc/articles/PMC7999308/ /pubmed/33801276 http://dx.doi.org/10.3390/v13030395 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Review Deutschmann, Janina Gramberg, Thomas SAMHD1 … and Viral Ways around It |
title | SAMHD1 … and Viral Ways around It |
title_full | SAMHD1 … and Viral Ways around It |
title_fullStr | SAMHD1 … and Viral Ways around It |
title_full_unstemmed | SAMHD1 … and Viral Ways around It |
title_short | SAMHD1 … and Viral Ways around It |
title_sort | samhd1 … and viral ways around it |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999308/ https://www.ncbi.nlm.nih.gov/pubmed/33801276 http://dx.doi.org/10.3390/v13030395 |
work_keys_str_mv | AT deutschmannjanina samhd1andviralwaysaroundit AT grambergthomas samhd1andviralwaysaroundit |