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:

A conserved sequence in the immunoglobulin JκCκ intron: possible enhancer element

Abstract

Several functionally important genetic elements (such as the TATA box, mRNA splice sequences, poly(A) addition signal) were first detected as short segments of unexplained sequence homology within non-coding regions of different genes. A short region of unknown sequence in the intron between the human Jκ and Cκ immunoglobulin coding regions was found to be sufficiently homologous to the corresponding segment of the mouse gene to form stable heteroduplexes1. Although no specific function has yet been definitely ascribed to this region (which we call the kappa intron conserved region, or KICR), some functional significance has been inferred from the findings that (1) activation of B lymphocytes induces a DNase hypersensitivity site in this region2,3 and (2) deletions including this region reduce expression of κ genes introduced into lymphoid cells4. To delineate the KICR more precisely and to test the generality of the sequence conservation in a third species, we have sequenced this region of the human and mouse genes and have examined the corresponding region of a recently cloned rabbit κ gene. We find a segment of about 130 base pairs (bp) that shows striking conservation in all three, species, demonstrating homology significantly higher than within the Cκ coding region itself. Two short sequences from the Jκ–Cκ intron that were noted by other investigators to be homologous to proposed ‘enhancer’ sequences both lie within the conserved region.

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. Hieter, P. A., Max, E. E., Seidman, J. G., Maizel, V. J. Jr & Leder, P. Cell 22, 197–207 (1980).

    Article  CAS  Google Scholar 

  2. Parslow, T. G. & Granner, D. K. Nature 299, 449–451 (1982).

    Article  ADS  CAS  Google Scholar 

  3. Chung, S.-Y., Folson, V. & Wooley, J. Proc. natn. Acad. Sci. U.S.A. 80, 2427–2431 (1983).

    Article  ADS  CAS  Google Scholar 

  4. Queen, C. & Baltimore, D. Cell (in the press).

  5. Max, E. E., Maizel, J. V. Jr & Leder, P. J. biol. Chem. 256, 5116–5120 (1981).

    CAS  PubMed  Google Scholar 

  6. Emorine, L., Dreher, K., Kindt, T. J. & Max, E. E. Proc. natn. Acad. Sci. U.S.A. (in the press).

  7. Maizel, J. V. Jr & Lenk, R. P. Proc. natn. Acad. Sci. U.S.A. 78, 7665–7669 (1981).

    Article  ADS  CAS  Google Scholar 

  8. Ravetch, J. V., Siebenlist, U., Korsmeyer, S., Waldmann, T. & Leder, P. Cell 27, 583–591 (1981).

    Article  CAS  Google Scholar 

  9. Hieter, P. A., Hollis, G. F., Korsmeyer, S. J., Waldmann, T. A. & Leder, P. Nature 294, 536–540 (1981).

    Article  ADS  CAS  Google Scholar 

  10. De La Salle, H., Jacq, C. & Slonimski, P. P. Cell 28, 721–732 (1982).

    Article  CAS  Google Scholar 

  11. Sutcliffe, J. G., Milner, R. J., Bloom, F. E. & Lerner, R. A. Proc. natn. Acad. Sci. U.S.A. 79, 4942–4946 (1982).

    Article  ADS  CAS  Google Scholar 

  12. Britten, R. J. & Davidson, E. H. Science 165, 349–357 (1969).

    Article  ADS  CAS  Google Scholar 

  13. Davies, R. W., Waring, R. B., Ray, J. A., Brown, T. A. & Scazzocchio, C. Nature 300, 719–724 (1982).

    Article  ADS  CAS  Google Scholar 

  14. Gruss, P., Dhar, R. & Khoury, G. Proc. natn. Acad. Sci. U.S.A. 78, 943 (1981).

    Article  ADS  CAS  Google Scholar 

  15. Benoist, C. & Chambon, P. Nature 290, 304 (1981).

    Article  ADS  CAS  Google Scholar 

  16. Mather, E. L. & Perry, R. P. Nucleic Acid Res. 9, 6855 (1981).

    Article  CAS  Google Scholar 

  17. Gillies, S. D., Morrison, S. L., Oi, V. T. & Tonegawa, S. Cell (in the press).

  18. Banerji, J., Olson, L. & Schaffner, W. Cell (in the press).

  19. Laimins, L. A., Kessel, M., Rosenthal, N. & Khoury, G. in Enhancers and Controlling Elements (ed. Gluzman, Y.) (Cold Spring Harbor Laboratory, New York, 1983).

    Google Scholar 

  20. Sanger, F., Nicklen, S. & Coulson, A. R. Proc. natn. Acad. Sci. U.S.A. 74, 5463–5467 (1977).

    Article  ADS  CAS  Google Scholar 

  21. Messing, J. & Vieira, J. Gene 19, 269–276 (1982).

    Article  CAS  Google Scholar 

  22. Maxam, A. M. & Gilbert, W. Meth. Enzym. 65, 499 (1980).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Emorine, L., Kuehl, M., Weir, L. et al. A conserved sequence in the immunoglobulin JκCκ intron: possible enhancer element. Nature 304, 447–449 (1983). https://doi.org/10.1038/304447a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/304447a0

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