Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Conserved organization of the human and murine T-cell receptor β-gene families

Abstract

Generation of an immune response depends on the interaction of haematopoietic cell types, among which T cells and their receptors are of central importance. The T-cell receptor is a heterodimer consisting of disulphide-linked α andβ -chains, each chain divided into variable (V) and constant (C) regions1–4. Theβ -chain is encoded by the rearrangement of separate variable ( Vβ diversity (Dβ) and joining (Jβ) gene segments during T-cell differenti- ment and evolution of the β-gene segments, we have constructed a physical map of the human T-cell receptor β -chain family containing 40 Vβ gene segments as well as both Cβp gene clusters. A comparison of the published nucleotide sequences of human and murine Vβ gene segments reveals 12 examples of gene segments sharing 65% or more interspecies homology. The relative order of these human and murine Vβ gene segment homologues is also conserved along the chromosome, apart from more extensive human gene duplication, presumably as a consequence of con-straints imposed on evolutionary mechanisms operating to diversify these gene families or of selective pressures operating to maintain order.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Allison, J. P., Mclntyre, B. & Bloch, D. J. Immun. 129, 2293–2300 (1982).

    CAS  PubMed  Google Scholar 

  2. Haskins, K. et al. J. exp. Med. 157, 1149–1169 (1983).

    Article  CAS  PubMed  Google Scholar 

  3. Kappler, J. et al. Cell 35, 295–302 (1983).

    Article  CAS  PubMed  Google Scholar 

  4. Meuer, S. C. et al. J. exp. Med. 157, 705–719 (1983).

    Article  CAS  PubMed  Google Scholar 

  5. Yanagi, Y. et al. Nature 308, 145–149 (1984).

    Article  ADS  CAS  PubMed  Google Scholar 

  6. Siu, G. et al. Cell 37, 393–401 (1984).

    Article  CAS  PubMed  Google Scholar 

  7. Lai, E., Barth, R. & Hood, L. Proc. natn. Acad. Sci. U.S.A. 84, 3846–3850 (1987).

    Article  ADS  CAS  Google Scholar 

  8. Carle, G. F., Frank, M. & Olson, M. V. Science 232, 65–68 (1986).

    Article  ADS  CAS  PubMed  Google Scholar 

  9. Kronenberg, M. et al. Nature 313, 647–653 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  10. Concannon, P., Pickering, L. A., Kung, P. & Hood, L. Proc. natn. Acad. Sci. U.S.A. 83, 6598–6602 (1986).

    Article  ADS  CAS  Google Scholar 

  11. Concannon, P., Gatti, R. A. & Hood, L. J. exp. Med. 165, 1130–1140 (1987).

    Article  CAS  PubMed  Google Scholar 

  12. Chou, H. S. Proc. natn. Acad. Sci. U.S.A. 84, 1992–1996 (1987).

    Article  ADS  CAS  Google Scholar 

  13. Chou, H. S. et al. Science 238, 545–548 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  14. Pech, M. et al. J. molec. Biol. 176, 189–204 (1984).

    Article  CAS  PubMed  Google Scholar 

  15. Kodaira, M. K. et al. J. molec. Biol. 190, 529–541 (1986}.

    Article  CAS  PubMed  Google Scholar 

  16. Patten, P. et al. Nature 312, 40–46 (1984).

    Article  ADS  CAS  PubMed  Google Scholar 

  17. Siu, G., Strauss, E. C., Lai, E. & Hood, L. J. exp. Med. 164, 1600–1614 (1986).

    Article  CAS  PubMed  Google Scholar 

  18. Fritsch, E. F., Lawn, R. M. & Maniatis, T. Cell 19, 959–972 (1982).

    Article  Google Scholar 

  19. Eickbish, T. H. & Kafatos, E. C. Cell 29, 633–643 (1982).

    Article  Google Scholar 

  20. Yancopoulos, G. D. et al. Nature 311, 727–733.

  21. Perlmutter, R. M., Kearney, J. F., Chang, S. P. & Hood, L. Science 227, 1597–1601 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  22. Schroeder, H. W., Hillson, J. L. & Perlmutter, R. Science 238, 791–793 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  23. Popko, B. et al. Cell 48, 713–721 (1987).

    Article  CAS  PubMed  Google Scholar 

  24. Reed, K. C. & Mann, D. A. Nucleic Acids Res. 13, 7207–7221 (1985).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Feinberg, A. P. & Vogelstein, B. Analyt. Biochem. 132, 6–13 (1983).

    Article  CAS  PubMed  Google Scholar 

  26. Singer, P. A., McEvilly, R. J., Noonan, D. J., Dixon, F. J. & Theofilopoulos, A. N. Proc. natn. Acad. Sci. U.S.A. 83, 7018–7022 (1986).

    Article  ADS  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lai, E., Concannon, P. & Hood, L. Conserved organization of the human and murine T-cell receptor β-gene families. Nature 331, 543–546 (1988). https://doi.org/10.1038/331543a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/331543a0

This article is cited by

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.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing