| Literature DB >> 26580513 |
Feifei Wang1, Corine St Gelais1, Suresh de Silva1, Hong Zhang2, Yu Geng2, Caitlin Shepard3, Baek Kim3, Jacob S Yount4, Li Wu5.
Abstract
Human SAMHD1 (hSAMHD1) restricts HIV-1 infection in non-dividing cells by depleting intracellular dNTPs to limit viral reverse transcription. Phosphorylation of hSAMHD1 at threonine (T) 592 by cyclin-dependent kinase (CDK) 1 and CDK2 negatively regulates HIV-1 restriction. Mouse SAMHD1 (mSAMHD1) restricts HIV-1 infection in non-dividing cells, but whether its phosphorylation regulates retroviral restriction is unknown. Here we identified six phospho-sites of mSAMHD1, including T634 that is homologous to T592 of hSAMHD1 and phosphorylated by CDK1 and CDK2. We found that wild-type (WT) mSAMHD1 and a phospho-ablative mutant, but not a phospho-mimetic mutant, restricted HIV-1 infection in differentiated U937 cells. Murine leukemia virus (MLV) infection of dividing NIH3T3 cells was modestly restricted by mSAMHD1 WT and phospho-mutants, but not by a dNTPase-defective mutant. Our results suggest that phosphorylation of mSAMHD1 at T634 by CDK1/2 negatively regulates its HIV-1 restriction in differentiated cells, but does not affect its MLV restriction in dividing cells.Entities:
Keywords: HIV-1; Infection; MLV; Mouse and human SAMHD1; Phosphorylation; Restriction
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Year: 2015 PMID: 26580513 PMCID: PMC4679491 DOI: 10.1016/j.virol.2015.10.024
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616