Abstract
HUMAN cytomegalovirus (HCMV) is a herpesvirus with a genome of 230 kilobases (Kb) encoding about 200 genes1. Although infection is generally innocuous, HCMV causes serious congenital and neonatal disease, and is a dangerous opportunistic pathogen in immune-deficient individuals2. We have identified a family of three HCMV genes which encode polypeptides containing seven putative membrane-spanning domains, and a series of well-defined motifs characteristic of the rhodopsin-like G protein-coupled receptors (GCRs). By these criteria all three of the HCMV sequences are homologous to cellular GCRs. Members of this receptor family function in visual signal transduction, regulation of homeostasis, and development, and include known and potential oncogenes3,4. These receptors are activated by photons or small molecules such as neurotransmitters, and glycoprotein hormones3,5,6. The finding of viral-encoded GCR homologues implies a further level of complexity in the interactions between HCMV and its host, and may provide a potential pathway for virally transformed cell proliferation. Their identification could permit the development of a novel class of antiviral drugs analogous to β-adrenergic receptor antagonists.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Chee, M. S. et al. Curr. Topics Microbiol. Immun. (in the press).
Alford, C. A. & Britt, W. J. in Virology (ed. Fields, B. N. et al.) 629–660 (Raven, New York, 1985).
Lefkowitz, R. J. & Caron, M. G. J. biol. Chem. 263, 4993–4996 (1988).
Jackson, T. R. Curr. Opin. Cell Biol. (in the press).
Firtel, R. A., van Haastert, P. J. M., Kimmel, A. R. & Devreotes, P. N. Cell 58, 235–239 (1989).
McFarland, K. C. et al. Science 245, 494–499 (1989).
Lipman, D. J. & Pearson, W. R. Science 227, 1435–1441 (1985).
Pearson, W. R. & Lipman, D. R. Proc. natn. Acad. Sci. U.S.A. 85, 2444–2448 (1988).
Staden, R. CABIOS 4, 53–60 (1988).
Staden, R. CABIOS 5, 89–96 (1989).
McGeoch, D. J. et al. J. gen. Virol. 69, 1531–1574 (1988).
Davison, A. J. & Scott, J. E. J. gen. Virol. 67, 1759–1816 (1986).
Baer, r. et al. Nature 310, 207–211 (1984).
Ruger, B. et al. J. Virol. 61, 446–453 (1987).
Mocarski, E. S., Pereira, L. & McCormick, A. L. J. gen. Virol. 69, 2613–2621 (1988).
Chang, C.-P., Vesole, D. H., Nelson, J., Oldstone, M. B. A. & Stinski, M. F. J. Virol. 63, 3330–3337 (1989).
Chang, C. P., Malone, C. L. & Stinski, M. F. J. Virol. 63 281–290 (1989).
Gretch, D. R., Kari, B., Gehrz, R. C. & Stinski, M. F. J. Virol. 62, 1956–1962 (1988).
Gretch, D. R. & Stinski, M. F. Virology 174, 522–532 (1990).
Kozak, M. Nucleic Acids Res. 9, 5233–5252 (1981).
Weston, K. & Barrell, B. G. J. molec. Biol. 192, 177–208 (1986).
Libert, F. et al. Science 244, 569–572 (1989).
Fliesler, S. J. & Basiner, S. F. Proc. natn. Acad. Sci. U.S.A. 82, 1116–1120 (1985).
Karnik, S. S., Sakmar, T. P., Chen, H.-B. & Khorana, H. G. Proc. natn. Acad. Sci. U.S.A. 85, 8459–8463 (1988).
Dixon, R. A. F. et al. EMBO J. 6, 3269–3275 (1987).
Brandl, C. J. & Deber, C. M. Proc. natn. Acad. Sci. U.S.A. 83, 917–921 (1986).
Strader, C. D. et al. Proc. natn. Acad. Sci. U.S.A. 84, 4384–4388 (1987).
Dohlman, H. G., Caron, M. G., Strader, C. D., Amlaiky, N. & Lefkowitz, R. J. Biochemistry 27, 1813–1817 (1988).
Dixon, R. A. F., Sigal, I. S. & Strader, C. D. Cold Spring Harb. Symp. quant. Biol. 53, 487–497 (1988).
Strader, C. D. et al. J. biol. Chem. 263, 10267–10271 (1988).
Franke, R. R., Sakmar, T. P., Oprian, D. D. & Khorana, H. G. J. biol. Chem. 263, 2119–2122 (1988).
Sibley, D. R., Benovic, J. L., Caron, M. G. & Lefkowitz, R. J. Cell 48, 913–922 (1987).
Fickenscher, H., Stamminger, T., Ruger, R. & Fleckenstein, B. J. gen. Virol. 70, 107–123 (1989).
Hunninghake, G. W., Monick, M. M., Liu, B. & Stinski, M. F. J. Virol. 63, 3026–3033 (1989).
Stinski, M. F. J. Virol. 23, 751–767 (1977).
Julius, D., Livelli, T. J., Jessell, T. M. & Axel, R. Science 244, 1057–1062 (1989).
Barbacid, M. A. Rev. Biochem. 56, 779–827 (1987).
Geder, L. in Oncogenic Herpesviruses, Vol. 2, 47–60 (ed. Rapp, F.) (CRC, Florida, 1980).
Black, J. Science 245, 486–493 (1989).
McKinlay, M. A. & Rossmann, M. G. A. Rev. Pharmac. Toxicol. 29, 111–122 (1989).
Barton, G. J. & Sternberg, M. J. E. J. molec. Biol. 198, 327–337 (1987).
McCaldon, P. & Argos, P. Proteins 4, 99–122 (1988).
Oram, J. D. et al. J. gen. Virol. 59, 111–129 (1982).
Sanger, F., Nicklen, S. & Coulson, A. R. Proc. natn. Acad. Sci. U.S.A. 74, 5463–5467 (1977).
Bankier, A. T., Weston, K. M. & Barrell, B. G. Meth. Enzym. 155, 51–93 (1987).
Jahn, G. et al. J. Virol. 61, 1358–1367 (1987).
Nathans, J. A. Rev. Neurosci. 10, 163–194 (1987).
O'Dowd, B. F., Lefkowitz, R. J. & Caron, m. G. A. Rev. Neurosci. 12, 67–83 (1989).
Fargin, A. et al. Nature 335, 358–360 (1988).
Kobilka, B. K. et al. Proc. natn. Acad. Sci. U.S.A. 84, 46–50 (1987).
Masu, Y. et al. Nature 329, 836–838 (1987).
Kubo, T. et al. Nature 323, 411–416 (1986).
Nathans, J. & Hogness, D. S. Cell 34, 807–814 (1983).
Young, D., Waitches, G., Birchmeier, C., Fasano, O. & Wigler, M. Cell 45, 711–719 (1986).
Jackson, T. R., Blair, L. A. C., Marshall, J., Goedert, M. & Hanley, M. R. Nature 335, 437–440 (1988).
Klein, P. S. et al. Science 241, 1467–1472 (1988).
Hagen, D. C., McCaffrey, G. & Sprague Jr, G. F. Proc. natn. Acad. Sci. U.S.A. 83, 1418–1422 (1986).
Stockwell, P. A. Trends biochem. Sci. 13, 322–324 (1988).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Chee, M., Satchwell, S., Preddie, E. et al. Human cytomegalovirus encodes three G protein-coupled receptor homologues. Nature 344, 774–777 (1990). https://doi.org/10.1038/344774a0
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1038/344774a0
This article is cited by
-
Selective targeting of ligand-dependent and -independent signaling by GPCR conformation-specific anti-US28 intrabodies
Nature Communications (2021)
-
Emerging roles of cytomegalovirus-encoded G protein-coupled receptors during lytic and latent infection
Medical Microbiology and Immunology (2019)
-
Identification and functional characterisation of 5-HT4 receptor in sea cucumber Apostichopus japonicus (Selenka)
Scientific Reports (2017)
-
The human cytomegalovirus chemokine receptor homolog encoded by US27
Virus Genes (2017)
-
DNA repair mechanisms and human cytomegalovirus (HCMV) infection
Folia Microbiologica (2015)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.