A model for cofactor use during HIV-1 reverse transcription and nuclear entry

Curr Opin Virol. 2014 Feb;4(100):32-6. doi: 10.1016/j.coviro.2013.11.003. Epub 2014 Jan 14.

Abstract

Lentiviruses have evolved to infect and replicate in a variety of cell types in vivo whilst avoiding the powerful inhibitory activities of restriction factors or cell autonomous innate immune responses. In this review we offer our opinions on how HIV-1 uses a series of host proteins as cofactors for infection. We present a model that may explain how the capsid protein has a fundamental role in the early part of the viral lifecycle by utilising cyclophilin A (CypA), cleavage and polyadenylation specificity factor-6 (CPSF6), Nup358 and TNPO3 to orchestrate a coordinated process of DNA synthesis, capsid uncoating and integration targeting that evades innate responses and promotes integration into preferred areas of chromatin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Active Transport, Cell Nucleus*
  • Cyclophilin A / metabolism
  • HIV Core Protein p24 / metabolism
  • HIV-1 / physiology*
  • Host-Pathogen Interactions*
  • Humans
  • Molecular Chaperones / metabolism
  • Nuclear Pore Complex Proteins / metabolism
  • Reverse Transcription*
  • beta Karyopherins / metabolism
  • mRNA Cleavage and Polyadenylation Factors / metabolism

Substances

  • HIV Core Protein p24
  • Molecular Chaperones
  • Nuclear Pore Complex Proteins
  • TNPO3 protein, human
  • beta Karyopherins
  • cleavage factor Im, human
  • mRNA Cleavage and Polyadenylation Factors
  • ran-binding protein 2
  • Cyclophilin A