The restriction factors of human immunodeficiency virus

J Biol Chem. 2012 Nov 30;287(49):40875-83. doi: 10.1074/jbc.R112.416925. Epub 2012 Oct 5.

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

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • APOBEC Deaminases
  • Animals
  • Antigens, CD / metabolism
  • Cytidine Deaminase
  • Cytosine Deaminase / metabolism
  • DNA, Complementary / metabolism
  • GPI-Linked Proteins / metabolism
  • Gene Expression Regulation, Viral
  • Genome, Viral
  • HIV-1 / metabolism*
  • Host-Pathogen Interactions
  • Humans
  • Immunity, Innate
  • Macaca
  • Models, Biological
  • Monomeric GTP-Binding Proteins / chemistry
  • Reverse Transcription
  • SAM Domain and HD Domain-Containing Protein 1
  • T-Lymphocytes / virology
  • Viral Proteins / metabolism
  • Virus Replication

Substances

  • Antigens, CD
  • BST2 protein, human
  • DNA, Complementary
  • GPI-Linked Proteins
  • Viral Proteins
  • SAM Domain and HD Domain-Containing Protein 1
  • SAMHD1 protein, human
  • Cytosine Deaminase
  • APOBEC Deaminases
  • APOBEC3 proteins, human
  • Cytidine Deaminase
  • Monomeric GTP-Binding Proteins