Phosphorylation of murine SAMHD1 regulates its antiretroviral activity
| Autor: | Wittmann, Sabine, Behrendt, Rayk, Eissmann, Kristin, Volkmann, Bianca, Thomas, Dominique, Ebert, Thomas, Cribier, Alexandra, Benkirane, Monsef, Hornung, Veit, Bouzas, Nerea Ferreirós, Gramberg, Thomas |
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| Jazyk: | angličtina |
| Rok vydání: | 2015 |
| Předmět: |
Threonine
MLV Virus Replication Cell Line SAM Domain and HD Domain-Containing Protein 1 Mice Medizinische Fakultät Virology SAMHD1 knockout mouse Animals Humans Myeloid Cells ddc:610 Phosphorylation Cells Cultured Monomeric GTP-Binding Proteins Mice Knockout Research Macrophages Reverse Transcription Leukemia Virus Murine Infectious Diseases HIV-1 RNA Viral SAMHD1 phosphorylation Retroviridae Infections |
| Zdroj: | Retrovirology |
| Popis: | BACKGROUND: Human SAMHD1 is a triphosphohydrolase that restricts the replication of retroviruses, retroelements and DNA viruses in noncycling cells. While modes of action have been extensively described for human SAMHD1, only little is known about the regulation of SAMHD1 in the mouse. Here, we characterize the antiviral activity of murine SAMHD1 with the help of knockout mice to shed light on the regulation and the mechanism of the SAMHD1 restriction and to validate the SAMHD1 knockout mouse model for the use in future infectivity studies. RESULTS: We found that endogenous mouse SAMHD1 restricts not only HIV-1 but also MLV reporter virus infection at the level of reverse transcription in primary myeloid cells. Similar to the human protein, the antiviral activity of murine SAMHD1 is regulated through phosphorylation at threonine 603 and is limited to nondividing cells. Comparing the susceptibility to infection with intracellular dNTP levels and SAMHD1 phosphorylation in different cell types shows that both functions are important determinants of the antiviral activity of murine SAMHD1. In contrast, we found the proposed RNase activity of SAMHD1 to be less important and could not detect any effect of mouse or human SAMHD1 on the level of incoming viral RNA. CONCLUSION: Our findings show that SAMHD1 in the mouse blocks retroviral infection at the level of reverse transcription and is regulated through cell cycle-dependent phosphorylation. We show that the antiviral restriction mediated by murine SAMHD1 is mechanistically similar to what is known for the human protein, making the SAMHD1 knockout mouse model a valuable tool to characterize the influence of SAMHD1 on the replication of different viruses in vivo. |
| Databáze: | OpenAIRE |
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