[Capping strategies in RNA viruses]

Med Sci (Paris). 2012 Apr;28(4):423-9. doi: 10.1051/medsci/2012284021. Epub 2012 Apr 25.
[Article in French]

Abstract

Most viruses use the mRNA-cap dependent cellular translation machinery to translate their mRNAs into proteins. The addition of a cap structure at the 5' end of mRNA is therefore an essential step for the replication of many virus families. Additionally, the cap protects the viral RNA from degradation by cellular nucleases and prevents viral RNA recognition by innate immunity mechanisms. Viral RNAs acquire their cap structure either by using cellular capping enzymes, by stealing the cap of cellular mRNA in a process named "cap snatching", or using virus-encoded capping enzymes. Many viral enzymes involved in this process have recently been structurally and functionally characterized. These studies have revealed original cap synthesis mechanisms and pave the way towards the development of specific inhibitors bearing antiviral drug potential.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Acid Anhydride Hydrolases / chemistry
  • Acid Anhydride Hydrolases / genetics
  • Acid Anhydride Hydrolases / metabolism
  • Acid Anhydride Hydrolases / physiology
  • Animals
  • Eukaryotic Cells / metabolism
  • Eukaryotic Cells / physiology
  • Humans
  • Models, Biological
  • Models, Molecular
  • Nucleic Acid Conformation
  • Protein Structure, Quaternary / physiology
  • Protein Structure, Secondary / physiology
  • RNA Caps / chemistry
  • RNA Caps / genetics
  • RNA Caps / metabolism
  • RNA Caps / physiology*
  • RNA Processing, Post-Transcriptional / genetics
  • RNA Processing, Post-Transcriptional / physiology
  • RNA Viruses / chemistry
  • RNA Viruses / genetics*
  • RNA Viruses / metabolism*
  • RNA, Viral / chemistry
  • RNA, Viral / genetics
  • RNA, Viral / metabolism*

Substances

  • RNA Caps
  • RNA, Viral
  • Acid Anhydride Hydrolases
  • RNA triphosphatase