The rat cytomegalovirus R33-encoded G protein-coupled receptor signals in a constitutive fashion

Y.K. Gruijthuijsen, P. Casarosa, S.J.F. Kaptein, J.L.V. Broers, R. Leurs, C.A. Bruggeman, Martine J. Smit, Cornelis Vink

Research output: Contribution to journalArticlePopular

68 Citations (Scopus)


The rat cytomegalovirus (RCMV) R33 gene is conserved among all betaherpesviruses and encodes a protein (pR33) that shows sequence similarity with chemokine-binding G protein-coupled receptors (GPCRs). Previously, the physiological significance of the R33 gene was demonstrated by the finding that an RCMV strain with R33 deleted is severely attenuated in vivo and is unable to either enter or replicate in the salivary glands of infected rats. Here, we report that RCMV pR33 is expressed as a functional GPCR that signals in an agonist-independent manner in both COS-7 and Rat2 cells. Transient expression of pR33 in COS-7 cells results in constitutive activation of phospholipase C (PLC) due to coupling to G proteins of the G(q) class. Interestingly, PLC activation is partially inhibited by cotransfection with G(alpha)-transducin subunits, which indicates the involvement of G(betagamma) as well as Galpha subunits in pR33-mediated signaling. Surprisingly, PLC activation is also partially inhibited by addition of pertussis toxin (PTX), suggesting that pR33 activates not only G(q) but also G(i/0) proteins. The constitutive activation of G(i/0) proteins by pR33 is further demonstrated by the PTX-sensitive decrease of CRE-mediated transcription and the PTX-sensitive increase of both NF-kappaB- and SRE-mediated transcription. In contrast to its homolog of human herpesvirus 6B (pU12), pR33 does not bind RANTES
Original languageEnglish
Pages (from-to)1328-1338
JournalJournal of virology
Issue number3
Publication statusPublished - 2002


Dive into the research topics of 'The rat cytomegalovirus R33-encoded G protein-coupled receptor signals in a constitutive fashion'. Together they form a unique fingerprint.

Cite this