Protein methylation is required to maintain optimal HIV-1 infectivity

Retrovirology. 2006 Dec 15:3:92. doi: 10.1186/1742-4690-3-92.

Abstract

Background: Protein methylation is recognized as a major protein modification pathway regulating diverse cellular events such as protein trafficking, transcription, and signal transduction. More recently, protein arginine methyltransferase activity has been shown to regulate HIV-1 transcription via Tat. In this study, adenosine periodate (AdOx) was used to globally inhibit protein methyltransferase activity so that the effect of protein methylation on HIV-1 infectivity could be assessed.

Results: Two cell culture models were used: HIV-1-infected CEM T-cells and HEK293T cells transfected with a proviral DNA plasmid. In both models, AdOx treatment of cells increased the levels of virion in culture supernatant. However, these viruses had increased levels of unprocessed or partially processed Gag-Pol, significantly increased diameter, and displayed reduced infectivity in a MAGI X4 assay. AdOx reduced infectivity equally in both dividing and non-dividing cells. However, infectivity was further reduced if Vpr was deleted suggesting virion proteins, other than Vpr, were affected by protein methylation. Endogenous reverse transcription was not inhibited in AdOx-treated HIV-1, and infectivity could be restored by pseudotyping HIV with VSV-G envelope protein. These experiments suggest that AdOx affects an early event between receptor binding and uncoating, but not reverse transcription.

Conclusion: Overall, we have shown for the first time that protein methylation contributes towards maximal virus infectivity. Furthermore, our results also indicate that protein methylation regulates HIV-1 infectivity in a complex manner most likely involving the methylation of multiple viral or cellular proteins and/or multiple steps of replication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / analogs & derivatives*
  • Adenosine / chemistry
  • Adenosine / pharmacology*
  • Cell Line
  • Fusion Proteins, gag-pol / metabolism
  • Gene Products, vpr / metabolism
  • HIV-1 / drug effects
  • HIV-1 / pathogenicity*
  • HIV-1 / ultrastructure
  • HeLa Cells
  • Humans
  • Methylation
  • Methyltransferases / antagonists & inhibitors*
  • Periodic Acid / pharmacology*
  • Proteins / metabolism*
  • T-Lymphocytes / virology
  • Virion / drug effects
  • Virion / metabolism
  • vpr Gene Products, Human Immunodeficiency Virus

Substances

  • Fusion Proteins, gag-pol
  • Gene Products, vpr
  • Proteins
  • vpr Gene Products, Human Immunodeficiency Virus
  • Periodic Acid
  • metaperiodate
  • Methyltransferases
  • Adenosine