Effects of T592 phosphomimetic mutations on tetramer stability and dNTPase activity of SAMHD1 can not explain the retroviral restriction defect

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Date
2016
Authors
Bhattacharya, Akash
Wang, Zhonghua
White, Tommy
Buffone, Cindy
Nguyen, Laura A.
Shepard, Caitlin N.
Kim, Baek
Demeler, Borries
Diaz-Griffero, Felipe
Ivanov, Dmitri N.
Journal Title
Journal ISSN
Volume Title
Publisher
Nature Publishing
Abstract
SAMHD1, a dNTP triphosphohydrolase, contributes to interferon signaling and restriction of retroviral replication. SAMHD1-mediated retroviral restriction is thought to result from the depletion of cellular dNTP pools, but it remains controversial whether the dNTPase activity of SAMHD1 is sufficient for restriction. The restriction ability of SAMHD1 is regulated in cells by phosphorylation on T592. Phosphomimetic mutations of T592 are not restriction competent, but appear intact in their ability to deplete cellular dNTPs. Here we use analytical ultracentrifugation, fluorescence polarization and NMR-based enzymatic assays to investigate the impact of phosphomimetic mutations on SAMHD1 tetramerization and dNTPase activity in vitro. We find that phosphomimetic mutations affect kinetics of tetramer assembly and disassembly, but their effects on tetramerization equilibrium and dNTPase activity are insignificant. In contrast, the Y146S/Y154S dimerization-defective mutant displays a severe dNTPase defect in vitro, but is indistinguishable from WT in its ability to deplete cellular dNTP pools and to restrict HIV replication. Our data suggest that the effect of T592 phosphorylation on SAMHD1 tetramerization is not likely to explain the retroviral restriction defect and we hypothesize that enzymatic activity of SAMHD1 is subject to additional cellular regulatory mechanisms that have not yet been recapitulated in vitro.
Description
Open access article. Creative Commons Attribution 4.0 International License (CC BY 4.0) applies
Keywords
Enzyme mechanisms , Phosphomimetic mutations , SAMHD1 , Tetramer stability , Retroviral
Citation
Bhattacharya, A., Wang, Z., White, T., Buffone, C., Nguyen, L. A., Shepard, C. N., Kim, B., Demeler, B., Diaz-Griffero, F., & Ivanov, D. N. (2016). Effects of T592 phosphomimetric mutations on tetramer stability and dNTPase activity of SAMHD1 can not explain the retroviral restriction defect. Scientific Reports, 6, Article 31353. https://doi.org/10.1038/srep31353
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