Wild-type levels of human immunodeficiency virus type 1 infectivity in the absence of cellular emerin protein

J Virol. 2007 Jan;81(1):166-72. doi: 10.1128/JVI.01953-06. Epub 2006 Oct 11.

Abstract

Preintegration complexes (PICs) mediate retroviral integration, and recent results indicate an important role for the inner nuclear membrane protein emerin in orienting human immunodeficiency virus type 1 (HIV-1) PICs to chromatin for integration. Two other host cell proteins, the barrier-to-autointegration factor (BAF) and lamina-associated polypeptide 2alpha (LAP2alpha), seemed to play a similar preintegrative role for Moloney murine leukemia virus (MMLV) in addition to HIV-1. In contrast, we determined efficient HIV-1 and MMLV infection of HeLa-P4 cells following potent down-regulation of emerin, BAF, or LAP2alpha protein by using short interfering RNA. Mouse embryo fibroblasts ablated for emerin protein through gene knockout support the same level of HIV-1 infection as cells derived from wild-type littermate control animals. As the expression of human emerin in mouse knockout cells fails to affect the level of infectivity achieved in its absence, we conclude that HIV-1 efficiently infects cells in the absence of emerin protein and, by extension, that emerin is not a universally important regulator of HIV-1 infectivity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Animals
  • DNA-Binding Proteins / antagonists & inhibitors
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Down-Regulation
  • HIV-1 / physiology*
  • HeLa Cells
  • Humans
  • Lamin Type A / genetics
  • Lamin Type A / metabolism
  • Leukemia Virus, Murine / pathogenicity
  • Membrane Proteins / antagonists & inhibitors
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Knockout
  • Molecular Sequence Data
  • Nuclear Proteins / antagonists & inhibitors
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • RNA Interference
  • RNA, Messenger / metabolism
  • Sequence Alignment

Substances

  • BANF1 protein, human
  • DNA-Binding Proteins
  • Lamin Type A
  • Membrane Proteins
  • Nuclear Proteins
  • RNA, Messenger
  • emerin
  • lamina-associated polypeptide 2