G3BP1 restricts HIV-1 replication in macrophages and T-cells by sequestering viral RNA

Virology. 2015 Dec:486:94-104. doi: 10.1016/j.virol.2015.09.007. Epub 2015 Sep 29.

Abstract

HIV-1 exploits the cellular machinery for replication and therefore several interactions with cellular factors take place, some of which are yet unknown. We identified GTPase-activating protein-(SH3 domain)-binding protein 1 (G3BP1) as a cellular factor that restricts HIV-1, by analyzing transcriptome profiles of in vitro-cytokine-activated macrophages that are non-permissive to HIV-1 replication. Silencing of G3BP1 by RNA interference resulted in increased HIV-1 replication in primary T-cells and macrophages, but did not affect replication of other retroviruses. G3BP1 specifically interacted with HIV-1 RNA in the cytoplasm, suggesting that it sequesters viral transcripts, thus preventing translation or packaging. G3BP1 was highly expressed in resting naïve or memory T-cells from healthy donors and HIV-1 infected patients, but significantly lower in IL-2-activated T-cells. These results strongly suggest that G3BP1 captures HIV-1 RNA transcripts and thereby restricts mRNA translation, viral protein production and virus particle formation.

Keywords: Activated T-cells; G3BP1; HIV-1; IFNgamma; Macrophage activation; Macrophage transcriptome profiles; TNFalpha.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • DNA Helicases
  • HIV Infections / enzymology*
  • HIV Infections / genetics
  • HIV Infections / virology
  • HIV-1 / genetics
  • HIV-1 / physiology*
  • Humans
  • Macrophages / metabolism*
  • Macrophages / virology
  • Poly-ADP-Ribose Binding Proteins
  • RNA Helicases
  • RNA Recognition Motif Proteins
  • RNA, Viral / genetics
  • RNA, Viral / metabolism*
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes / virology
  • Virus Replication*

Substances

  • Carrier Proteins
  • Poly-ADP-Ribose Binding Proteins
  • RNA Recognition Motif Proteins
  • RNA, Viral
  • DNA Helicases
  • G3BP1 protein, human
  • RNA Helicases