Integrase mutants defective for interaction with LEDGF/p75 are impaired in chromosome tethering and HIV-1 replication

J Biol Chem. 2005 Jul 8;280(27):25517-23. doi: 10.1074/jbc.M501378200. Epub 2005 Apr 25.

Abstract

The insertion of a DNA copy of its RNA genome into a chromosome of the host cell is mediated by the viral integrase with the help of mostly uncharacterized cellular cofactors. We have recently described that the transcriptional co-activator LEDGF/p75 strongly interacts with HIV-1 integrase. Here we show that interaction of HIV-1 integrase with LEDGF/p75 is important for viral replication. Using multiple approaches including two-hybrid interaction studies, random and directed mutagenesis, we could demonstrate that HIV-1 virus harboring a single mutation that disrupts integrase-LEDGF/p75 interaction, resulted in defective HIV-1 replication. Furthermore, we found that LEDGF/p75 tethers HIV-1 integrase to chromosomes and that this interaction may be important for the integration process and the replication of HIV-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Human / virology
  • Glutamine / metabolism
  • HIV Infections / genetics
  • HIV Infections / metabolism
  • HIV Infections / virology*
  • HIV Integrase / genetics*
  • HIV Integrase / metabolism*
  • HIV-1 / genetics
  • HIV-1 / growth & development*
  • HeLa Cells
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Virus Integration / physiology
  • Virus Replication / physiology

Substances

  • Intercellular Signaling Peptides and Proteins
  • lens epithelium-derived growth factor
  • Glutamine
  • HIV Integrase