Abstract
Cellular proteins called "restriction factors" can serve as powerful blockades to HIV replication, but the virus possesses elaborate strategies to circumvent these barriers. First, we discuss general hallmarks of a restriction factor. Second, we review how the viral Vif protein protects the viral genome from lethal levels of cDNA deamination by promoting APOBEC3 protein degradation; how the viral Vpu, Env, and Nef proteins facilitate internalization and degradation of the virus-tethering protein BST-2/tetherin; and how the viral Vpx protein prevents the premature termination of reverse transcription by degrading the dNTPase SAMHD1. These HIV restriction and counter-restriction mechanisms suggest strategies for new therapeutic interventions.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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APOBEC Deaminases
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Animals
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Antigens, CD / metabolism
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Cytidine Deaminase
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Cytosine Deaminase / metabolism
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DNA, Complementary / metabolism
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GPI-Linked Proteins / metabolism
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Gene Expression Regulation, Viral
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Genome, Viral
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HIV-1 / metabolism*
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Host-Pathogen Interactions
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Humans
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Immunity, Innate
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Macaca
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Models, Biological
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Monomeric GTP-Binding Proteins / chemistry
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Reverse Transcription
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SAM Domain and HD Domain-Containing Protein 1
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T-Lymphocytes / virology
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Viral Proteins / metabolism
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Virus Replication
Substances
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Antigens, CD
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BST2 protein, human
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DNA, Complementary
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GPI-Linked Proteins
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Viral Proteins
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SAM Domain and HD Domain-Containing Protein 1
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SAMHD1 protein, human
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Cytosine Deaminase
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APOBEC Deaminases
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APOBEC3 proteins, human
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Cytidine Deaminase
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Monomeric GTP-Binding Proteins