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:

Distinct NF-κB/Rel transcription factors are responsible for tissue-specific and inducible gene activation

Abstract

THE NF-κB/Rel family is a growing class of transcriptional regulators1–11 whose members share the conserved Rel-homology domain, involved in specific DNA binding and dimerization. They interact with the regulatory elements of many different genes and are involved in the regulation of lymphoid-specific and inducible transcription12. We tested whether these factors could alone activate a gene in transgenic mice. We report here that a minimal promoter containing three copies of a binding site for these proteins allows tissue-specific and inducible transgene activation. In lymphoid tissues constitutive transgene expression correlates with the presence of a constitutively active p50/RelB heterodimer. Other organs that only contain the p50 homodimer do not express the transgene. In contrast to this constitutive activity mediated by p50/RelB, the p50/p65 heterodimer (which is NF-κB) could confer inducible transgene activation in embryo fibroblasts. Thus two different members of the NF-κB/Rel family of transcriptional activators are involved in tissue-specific and inducible gene activation in transgenic mice.

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. Wilhelmsen, K. C., Eggleton, K. & Temin, H. M. J. Virol. 52, 172–182 (1984).

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Steward, R. Science 238, 692–694 (1987).

    Article  ADS  CAS  Google Scholar 

  3. Kieran, M. et al. Cell 62, 1007–1018 (1990).

    Article  CAS  Google Scholar 

  4. Gosh, S. et al. Cell 62, 1019–1029 (1990).

    Article  Google Scholar 

  5. Bours, V., Villalobos, J., Burd, P. R., Kelly, K. & Siebenlist, U. Nature 348, 76–80 (1990).

    Article  ADS  CAS  Google Scholar 

  6. Meyer, R. et al. Proc. natn. Acad. Sci. U.S.A. 88, 966–970 (1991).

    Article  ADS  CAS  Google Scholar 

  7. Nolan, G. P., Gosh, S., Liou, H.-C. Tempst, P. & Baltimore, D. Cell 64, 961–969 (1991).

    Article  CAS  Google Scholar 

  8. Ruben, S. M. et al. Science 251, 1490–1493 (1991).

    Article  ADS  CAS  Google Scholar 

  9. Schmid, R. M., Perkins, N. D., Duckett, C. S., Andrews, P. C. & Nabel, G. J. Nature 352, 733–736 (1991).

    Article  ADS  CAS  Google Scholar 

  10. Bours, V. et al. Molec. cell. Biol. 12, 685–695 (1992).

    Article  CAS  Google Scholar 

  11. Ryseck, R.-P. et al. Molec. cell. Biol. 12, 674–684 (1992).

    Article  CAS  Google Scholar 

  12. Lenardo, M. J. & Baltimore, D. Cell 58, 227–229 (1989).

    Article  CAS  Google Scholar 

  13. Pierce, J. W., Lenardo, M. & Baltimore, D. Proc. natn. Acad. Sci. U.S.A. 85, 1482–1486 (1988).

    Article  ADS  CAS  Google Scholar 

  14. Wirth, T. & Baltimore, D. EMBO J. 7, 3109–3113 (1988).

    Article  CAS  Google Scholar 

  15. Sen, R. & Baltimore, D. Cell 46, 705–716 (1986).

    Article  CAS  Google Scholar 

  16. Baldwin, A. S. Jr, Azizkhan, J. C., Jensen, D. E., Beg, A. A. & Coodly, L. R. Molec. cell. Biol. 11, 4943–4951 (1991).

    Article  CAS  Google Scholar 

  17. Sen, R. & Baltimore, D. Cell 47, 921–928 (1986).

    Article  CAS  Google Scholar 

  18. Nabel, G. & Baltimore, D. Nature 326, 711–713 (1987).

    Article  ADS  CAS  Google Scholar 

  19. Baeuerle, P. A. & Baltimore, D. in The Hormonal Control Regulation of Gene Transcription (eds Cohen, P. & Foulkes, J. G.) 423–446 (Elsevier-Biomedical, Amsterdam, 1991).

    Book  Google Scholar 

  20. Baeuerle, P. A. & Baltimore, D. Cell 53, 211–217 (1988).

    Article  CAS  Google Scholar 

  21. Yano, O. et al. EMBO J. 6, 3317–3324 (1987).

    Article  CAS  Google Scholar 

  22. Baldwin, A. S. Jr & Sharp, P. A. Proc. natn. Acad. Sci. U.S.A. 85, 723–727 (1988).

    Article  ADS  CAS  Google Scholar 

  23. Kang, S.-M., Tran, A.-C., Grilli, M. & Lenardo, M. J. Science 256, 1452–1456 (1992).

    Article  ADS  CAS  Google Scholar 

  24. Beg, A. A., Finco, T. S., Nantermet, P. V. & Baldwin, A. S. Jr Moiec. cell. Biol. 13, 3301–3310 (1993).

    CAS  Google Scholar 

  25. Schmitz, M. L. & Baeuerle, P. A. EMBO J. 10, 3805–3817 (1991).

    Article  CAS  Google Scholar 

  26. Annweiler, A., Müller, U. & Wirth, T. Nucleic Acids Res. 20, 1503–1509 (1992).

    Article  CAS  Google Scholar 

  27. Ausubel, F. M. et al. Current Protocols in Molecular Biology (Wiley, New York, 1989).

    Google Scholar 

  28. Robertson, E. J. in Teratocarcinomas and Embryonic Stem Cells: a Practical Approach (ed. Robertson, E. J.) 71–112 (IRL, Oxford, 1987).

    Google Scholar 

  29. Atchison, M. L. & Perry, R. P. Cell 48, 121–128 (1987).

    Article  CAS  Google Scholar 

  30. Dignam, J. D., Lebovitz, R. M. & Roeder, R. G. Nucleic Acids Res. 11, 1475–1489 (1983).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lernbecher, T., Müller, U. & Wirth, T. Distinct NF-κB/Rel transcription factors are responsible for tissue-specific and inducible gene activation. Nature 365, 767–770 (1993). https://doi.org/10.1038/365767a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/365767a0

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