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Rearrangement of two distinct T-cell γ-chain variable-region genes in human DNA

Abstract

Selective cloning procedures for T-cell-specific complementary DNAs have revealed the existence of a gene designated1 γ as well as the main antigen receptor α- and β-chain genes2–10. The γ-chain genes undergo rearrangement during T-cell differentiation but the patterns and complexity of such rearrangements differ markedly in mouse11–13 and human14. In mouse, a panel of cytotoxic T-lymphocyte clones exhibit the same rearrangement pattern with a γ-chain gene probe11 and a set of three γ-chain variable (V) genes have been identified in the DNA12. Clonal diversity in mouse seems to be confined to V–J (joining) regions11. In contrast, human T-cell lines exhibit diverse rearrangements14 suggestive of a family of differing Vγ genes variously rearranging to the two γ-chain constant (C) region genes14,15. Here we report the cloning of two very different Vγ genes rearranged to J segments upstream of the two human Cγ genes. Both Vγ genes are rearranged productively but nucleotide sequence comparison shows that they possess very little homology with each other. This shows that human T-cell Vγ genes exist which differ significantly from each other at the nucleotide level and that such diverse genes can be usefully rearranged in different T cells.

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References

  1. Saito, H. et al. Nature 309, 757–762 (1984).

    Article  ADS  CAS  Google Scholar 

  2. Chien, Y.-H. et al. Nature 312, 31–35 (1984).

    Article  ADS  CAS  Google Scholar 

  3. Gascoigne, N. R. J., Chien, Y.-H., Becker, D. M., Kavaler, J. & Davis, M. M. Nature 310, 387–391 (1984).

    Article  ADS  CAS  Google Scholar 

  4. Hedrick, S. M., Nielsen, E. A., Kavaler, J., Cohen. D I & Davis, M. M. Nature 308, 153–158 (1984).

    Article  ADS  CAS  Google Scholar 

  5. Saito, H. et al. Nature 312, 36–40 (1984).

    Article  ADS  CAS  Google Scholar 

  6. Sim, G. K. et al. Nature 312, 771–775 (1984).

    Article  ADS  CAS  Google Scholar 

  7. Sims, J. E., Tunnacliffe, A., Smith, W. S. & Rabbitts, T. H. Nature 312, 541–545 (1984).

    Article  ADS  CAS  Google Scholar 

  8. Siu, G. et al. Cell 37, 381–391 (1984).

    Article  Google Scholar 

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

    Article  ADS  CAS  Google Scholar 

  10. Yanagi, Y., Chan, A., Chin, B., Minden, M. & Mak, T. W. Proc. natn. Acad. Sci. U.S.A. 82, 3430–3434 (1985).

    Article  ADS  CAS  Google Scholar 

  11. Kranz, D. M. et al. Nature 313, 752–755 (1985).

    Article  ADS  CAS  Google Scholar 

  12. Hayday, A. C. et al. Cell 40, 259–269 (1985).

    Article  CAS  Google Scholar 

  13. Heilig, J. S. et al. Nature 317, 68–70 (1985).

    Article  ADS  CAS  Google Scholar 

  14. Lefranc, M.-P. & Rabbitts, T. H. Nature 316, 464–466 (1985).

    Article  ADS  CAS  Google Scholar 

  15. Murre, C. et al. Nature 316, 549–552 (1985).

    Article  ADS  CAS  Google Scholar 

  16. Baer, R., Chen, K. C., Smith, S. D. & Rabbitts, T. H. Cell 43, 705–713 (1985).

    Article  CAS  Google Scholar 

  17. Smith, S. D. et al. Cancer Res. 44, 5657–5660 (1984).

    CAS  PubMed  Google Scholar 

  18. Sanger, F., Coulson, A. R., Barrell, B. G., Smith, A. J. H. & Roe, B. A. J. molec. Biol. 143, 161–178 (1980).

    Article  CAS  Google Scholar 

  19. Staden, R. Nucleic Acids Res. 8, 3673–3694 (1980).

    Article  CAS  Google Scholar 

  20. Staden, R. Nucleic Acids Res. 12, 521–538 (1984).

    Article  CAS  Google Scholar 

  21. Karn, J., Matthes, H. W. D., Gait, M. J. & Brenner, S. Gene 32, 217–224 (1984).

    Article  CAS  Google Scholar 

  22. Vieira, J. & Messing, J. Gene 19, 259–268 (1982).

    Article  CAS  Google Scholar 

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Lefranc, MP., Forster, A. & Rabbitts, T. Rearrangement of two distinct T-cell γ-chain variable-region genes in human DNA. Nature 319, 420–422 (1986). https://doi.org/10.1038/319420a0

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