The virion host shutoff protein (UL41) of herpes simplex virus 1 is an endoribonuclease with a substrate specificity similar to that of RNase A

J Virol. 2006 Sep;80(18):9341-5. doi: 10.1128/JVI.01008-06.

Abstract

Earlier, our laboratory reported that purified glutathione S-transferase-virion host shutoff (GST-vhs) protein exhibited endoribonucleolytic activity in in vitro assays using as substrates in vitro-transcribed regions of IEX-1 mRNA. Here, we report that studies of the cleavage patterns of synthetic RNA oligonucleotides defined the activity of GST-vhs as being similar to that of RNase A. Thus, GST-vhs cleaved the RNA at the 3' end of single-stranded cytidine and uridine residues. Since the GST-mvhs nuclease-defective mutant protein failed to cleave the synthetic RNAs, the results unambiguously attribute the activity to vhs.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Base Sequence
  • Endoribonucleases / chemistry*
  • Glutathione Transferase / metabolism
  • Herpesvirus 1, Human / enzymology*
  • Herpesvirus 1, Human / genetics*
  • Molecular Sequence Data
  • Nucleic Acid Conformation
  • RNA / chemistry
  • RNA, Messenger / metabolism
  • RNA, Viral / genetics
  • Ribonuclease, Pancreatic / chemistry*
  • Substrate Specificity
  • Viral Proteins / chemistry
  • Viral Proteins / genetics*

Substances

  • RNA, Messenger
  • RNA, Viral
  • Ul41 protein, Human herpesvirus 1
  • Viral Proteins
  • RNA
  • Glutathione Transferase
  • Endoribonucleases
  • Ribonuclease, Pancreatic