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.

  • News & Views
  • Published:

E-cadherin and Hakai: signalling, remodeling or destruction?

Activation of tyrosine kinase receptors in epithelial cells results in the rapid disassembly of E-cadherin-mediated cell–cell adhesions. New research has identified Hakai, an E3-ubiquitin-ligase related to Cbl that binds E-cadherin in a tyrosine phosphorylation-dependent manner. By promoting the endocytosis and dynamic recycling or destruction of E-cadherin complexes, Hakai may control epithelial–mesenchymal transitions under physiological and pathological conditions.

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

Relevant articles

Open Access articles citing this article.

Access options

Buy this article

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

Figure 1: A model for Hakai in the dynamic regulation of E-cadherin-mediated adherens junction.

References

  1. Kemler, R. Semin. Cell Biol. 3, 149–155 (1992).

    Article  CAS  PubMed  Google Scholar 

  2. Takeichi, M. Curr. Opin. Cell Biol. 7, 619–627 (1995).

    Article  CAS  PubMed  Google Scholar 

  3. Gumbiner, B. M. J. Cell Biol. 148, 399–404 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Fujita et al. Nature Cell Biol. 4, 222–231 (2002).

    Article  CAS  PubMed  Google Scholar 

  5. Bonifacino, J. S. & Weissman, A. M. Annu. Rev. Cell Dev. Biol. 14, 19–57 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Hicke, L. & Riezman, H. Cell 84, 277–287 (1996).

    Article  CAS  PubMed  Google Scholar 

  7. Kamei, T. et al. Oncogene 18, 6776–6784 (1999).

    Article  CAS  PubMed  Google Scholar 

  8. Birchmeier, W. & Behrens, J. Biochim. Biophys. Acta 1198, 11–26 (1994).

    CAS  PubMed  Google Scholar 

  9. Batlle, E. et al. Nature Cell Biol. 2, 84–89 (2000).

    Article  CAS  PubMed  Google Scholar 

  10. Calautti, E. et al. J. Cell Biol. 156, 137–148 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Angst, B. D., Marcozzi, C. & Magee, A. I. J. Cell Sci. 114, 625–626 (2001).

    CAS  PubMed  Google Scholar 

  12. Patterson, C. Sci. STKE (cited 22 Jan 2002), http://stke.sciencemag.org/cgi/content/full/OC_sigtrans;2002/116/pe4 (2002).

  13. Di Fiore, P. P. & De Camilli, P. Cell 106, 1–4 (2001).

    Article  CAS  PubMed  Google Scholar 

  14. Thien, C. B. & Langdon, W. Y. Nature Rev. Mol. Cell Biol. 2, 294–307 (2001).

    Article  CAS  Google Scholar 

  15. Pece, S. & Gutkind, J. S. J. Biol. Chem. 275, 41227–41233 (2000).

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pece, S., Gutkind, J. E-cadherin and Hakai: signalling, remodeling or destruction?. Nat Cell Biol 4, E72–E74 (2002). https://doi.org/10.1038/ncb0402-e72

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/ncb0402-e72

This article is cited by

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