Molecular mimicry of the antigen receptor signalling motif by transmembrane proteins of the Epstein-Barr virus and the bovine leukaemia virus
- PMID: 15335726
- DOI: 10.1016/0960-9822(93)90196-u
Molecular mimicry of the antigen receptor signalling motif by transmembrane proteins of the Epstein-Barr virus and the bovine leukaemia virus
Abstract
Background: Many transmembrane proteins of eukaryotic cells have only a short cytoplasmic tail of 10 - 100 amino acids, which has no obvious catalytic function. These tails are thought to be involved either in signal transduction or in the association of transmembrane proteins with the cytoskeleton. We have previously identified, in the cytoplasmic tails of components of B and T lymphocyte antigen receptors, an amino-acid motif that is required for signalling. The same motif is also found in the cytoplasmic tails of two viral proteins: the latent membrane protein, LMP2A, of Epstein Barr virus and the envelope protein, gp30, of bovine leukaemia virus. Interestingly, both viruses can activate infected B lymphocytes to proliferate, as does signalling by the B-cell receptor.
Results: In this study, we show that the cytoplasmic tails of the two viral proteins, and the cytoplasmic tail of the B-cell receptor immunoglobulin-alpha chain, when linked to CD8 in chimeric transmembrane proteins, can transduce signals in B cells. Cross-linking of these chimeric receptors activates B-cell protein tyrosine kinases and results in calcium mobilization. Furthermore, these cytoplasmic sequences are also protein tyrosine kinase substrates and may interact with cytosolic proteins carrying SH2 protein-protein interaction domains.
Conclusion: Our findings suggest that viral transmembrane proteins can mimic the antigen-induced stimulation of the B-cell antigen receptor and thus can influence the activation and/or survival of infected B lymphocytes.
Similar articles
-
The (YXXL/I)2 signalling motif found in the cytoplasmic segments of the bovine leukaemia virus envelope protein and Epstein-Barr virus latent membrane protein 2A can elicit early and late lymphocyte activation events.EMBO J. 1993 Dec 15;12(13):5105-12. doi: 10.1002/j.1460-2075.1993.tb06205.x. EMBO J. 1993. PMID: 8262054 Free PMC article.
-
The immunoreceptor tyrosine-based activation motif of Epstein-Barr virus LMP2A is essential for blocking BCR-mediated signal transduction.Virology. 1997 Sep 1;235(2):241-51. doi: 10.1006/viro.1997.8690. Virology. 1997. PMID: 9281504
-
Epstein-Barr virus LMP2A alters in vivo and in vitro models of B-cell anergy, but not deletion, in response to autoantigen.J Virol. 2005 Jun;79(12):7355-62. doi: 10.1128/JVI.79.12.7355-7362.2005. J Virol. 2005. PMID: 15919890 Free PMC article.
-
Epstein-Barr virus protein LMP2A regulates reactivation from latency by negatively regulating tyrosine kinases involved in sIg-mediated signal transduction.Infect Agents Dis. 1994 Apr-Jun;3(2-3):128-36. Infect Agents Dis. 1994. PMID: 7812651 Review.
-
Latent Membrane Protein 2 (LMP2).Curr Top Microbiol Immunol. 2015;391:151-80. doi: 10.1007/978-3-319-22834-1_5. Curr Top Microbiol Immunol. 2015. PMID: 26428374 Review.
Cited by
-
Role of the proline-rich motif of bovine leukemia virus transmembrane protein gp30 in viral load and pathogenicity in sheep.J Virol. 2001 Sep;75(17):8082-9. doi: 10.1128/jvi.75.17.8082-8089.2001. J Virol. 2001. PMID: 11483753 Free PMC article.
-
Deregulated signal transduction by the K1 gene product of Kaposi's sarcoma-associated herpesvirus.Proc Natl Acad Sci U S A. 1999 May 11;96(10):5704-9. doi: 10.1073/pnas.96.10.5704. Proc Natl Acad Sci U S A. 1999. PMID: 10318948 Free PMC article.
-
Dileucine and YXXL motifs in the cytoplasmic tail of the bovine leukemia virus transmembrane envelope protein affect protein expression on the cell surface.J Virol. 2004 Aug;78(15):8301-11. doi: 10.1128/JVI.78.15.8301-8311.2004. J Virol. 2004. PMID: 15254202 Free PMC article.
-
Envelope proteins containing single amino acid substitutions support a structural model of the receptor-binding domain of bovine leukemia virus surface protein.J Virol. 2002 Nov;76(21):10861-72. doi: 10.1128/jvi.76.21.10861-10872.2002. J Virol. 2002. PMID: 12368329 Free PMC article.
-
The YXXL signalling motifs of the bovine leukemia virus transmembrane protein are required for in vivo infection and maintenance of high viral loads.J Virol. 1995 Jul;69(7):4137-41. doi: 10.1128/JVI.69.7.4137-4141.1995. J Virol. 1995. PMID: 7769672 Free PMC article.
LinkOut - more resources
Full Text Sources
Research Materials