HIV-1 infection requires a functional integrase NLS

Mol Cell. 2001 May;7(5):1025-35. doi: 10.1016/s1097-2765(01)00240-4.

Abstract

HIV-1 is able to infect nondividing cells productively in part because the postentry viral nucleoprotein complexes are actively imported into the nucleus. In this manuscript, we identify a novel nuclear localization signal (NLS) in the viral integrase (IN) protein that is essential for virus replication in both dividing and nondividing cells. The IN NLS stimulates the efficient nuclear accumulation of viral DNA as well as virion-derived IN protein during the initial stages of infection but is dispensable for catalytic function. Because this NLS is required for infection irrespective of target cell proliferation, we suggest that interactions between uncoated viral nucleoprotein complexes and the host cell nuclear import machinery are critical for HIV-1 infection of all cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Active Transport, Cell Nucleus / drug effects
  • Amino Acid Sequence
  • Cell Nucleus / virology
  • Cells, Cultured
  • DNA, Viral / biosynthesis
  • HIV Infections / enzymology*
  • HIV Integrase / chemistry
  • HIV Integrase / genetics
  • HIV Integrase / metabolism*
  • HIV-1*
  • HeLa Cells
  • Humans
  • Leukocytes, Mononuclear / virology
  • Mutagenesis, Site-Directed
  • Nuclear Localization Signals / genetics
  • Nuclear Localization Signals / pharmacology*
  • Nuclear Localization Signals / physiology
  • Protein Structure, Tertiary
  • Sequence Alignment
  • Subcellular Fractions / chemistry
  • T-Lymphocytes / virology

Substances

  • DNA, Viral
  • Nuclear Localization Signals
  • HIV Integrase