Identification of the human cytomegalovirus G protein-coupled receptor homologue encoded by UL33 in infected cells and enveloped virus particles

Virology. 1996 Nov 1;225(1):111-25. doi: 10.1006/viro.1996.0579.


Human cytomegalovirus (HCMV), strain AD169, contains four genes (US27, US28, UL33, and UL78) that encode putative homologues of cellular G protein-coupled receptors (GCRs). GCRs transduce extracellular signals to alter intracellular processes, and there is evidence that HCMV may elicit such changes at early times following infection. The US27, US28, and UL33 genes are transcribed during infection, and the US28 gene product has been found to be a functional receptor for the beta-chemokine class of immune modulators. The US27, UL33, and UL78 gene products have not been described and we have concentrated on identifying the UL33 protein because it is the most highly conserved of the GCR homologues among the human beta and gamma herpesviruses. We report here cloning UL33 into a recombinant baculovirus (rBV) and expressing it in insect cells; constructing a mutant HCMV with a disrupted UL33 gene; and identifying the UL33 protein in HCMV-infected cells and virus particles. Our results demonstrate that the UL33 protein (i) is expressed as a approximately 36-kDa, heat-aggregatable protein in rBV-infected cells, (ii) is modified heterogeneously by asparagine-linked glycosylation and expressed as a > or = 58-kDa glycoprotein that is present in the region of the cytoplasmic inclusions in HCMV-infected fibroblasts, (iii) is present in virions and two other enveloped virus particles, and (iv) is not essential for growth of HCMV in human foreskin fibroblast cultures.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amidohydrolases
  • Amino Acid Sequence
  • Animals
  • Asparagine / metabolism
  • Cell Line
  • Cloning, Molecular
  • Cytomegalovirus / chemistry*
  • Cytomegalovirus / genetics
  • Cytomegalovirus / growth & development
  • Fibroblasts / virology
  • GTP-Binding Proteins*
  • Glycosylation
  • Humans
  • Inclusion Bodies, Viral / virology
  • Molecular Sequence Data
  • Molecular Weight
  • Nucleopolyhedroviruses / genetics
  • Peptide Fragments / analysis
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase
  • RNA Splicing
  • Receptors, Cell Surface / genetics*
  • Recombinant Proteins
  • Sequence Homology, Amino Acid
  • Spodoptera
  • Viral Proteins / analysis
  • Viral Proteins / chemistry*
  • Viral Proteins / genetics
  • Viral Proteins / physiology
  • Virion / chemistry


  • Peptide Fragments
  • Receptors, Cell Surface
  • Recombinant Proteins
  • Viral Proteins
  • Asparagine
  • Amidohydrolases
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase
  • GTP-Binding Proteins