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:

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

Abstract

The p63 gene, a homologue of the tumour-suppressor p53 (15), is highly expressed in the basal or progenitor layers of many epithelial tissues1. Here we report that mice homozygous for a disrupted p63 gene have major defects in their limb, craniofacial and epithelial development. p63 is expressed in the ectodermal surfaces of the limb buds, branchial arches and epidermal appendages, which are all sites of reciprocal signalling that direct morphogenetic patterning of the underlying mesoderm. The limb truncations are due to a failure to maintain the apical ectodermal ridge, a stratified epithelium, essential for limb development. The embryonic epidermis of p63 −/− mice undergoes an unusual process of non-regenerative differentiation, culminating in a striking absence of all squamous epithelia and their derivatives, including mammary, lacrymal and salivary glands. Taken together, our results indicate that p63 is critical for maintaining the progenitor-cell populations that are necessary to sustain epithelial development and morphogenesis.

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

Figure 1: Disruption of the p63 gene in mice.
Figure 2: Defective limb development in p63−/− mice.
Figure 3: Defects in stratified epithelial differentiation in p63-deficient mice.
Figure 4: Expression of differentiation markers in p63−/− epidermis.
Figure 5: Model for p63 in maintaining the proliferative capacity of epithelial progenitor cells.

Similar content being viewed by others

References

  1. Yang, A. et al. p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. Mol. Cell 2, 305–316 (1998).

    Article  CAS  Google Scholar 

  2. Augustin, M., Bamberger, C., Paul, D. & Schmale, H. Cloning and chromosomal mapping of the human p53-related KET gene to chromosome 3q27 and its murine homolog Ket to mouse chromosome 16. Mamm. Genome 11, 899–902 (1998).

    Article  Google Scholar 

  3. Osada, M. et al. Cloning and functional analysis of human p51, which structurally and functionally resembles p53. Nature Med. 4, 839–843 (1998).

    Article  CAS  Google Scholar 

  4. Trink, B. et al. Anew human p53 homologue. Nature Med. 4, 747–748 (1998).

    Article  Google Scholar 

  5. Ko, L. J. & Prives, C. p53: puzzle and paradigm. Genes Dev. 10, 1054–1072 (1996).

    Article  CAS  Google Scholar 

  6. Kaghad, M. et al. Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell 90, 809–819 (1997).

    Article  CAS  Google Scholar 

  7. Mansour, S. L., Thomas, K. R. & Capecchi, M. R. Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes. Nature 336, 348–352 (1988).

    Article  ADS  CAS  Google Scholar 

  8. Tickle, C. Vertebrate limb development. Curr. Opin. Genet. Dev. 5, 478–484 (1995).

    Article  CAS  Google Scholar 

  9. Johnson, R. L. & Tabin, C. J. Molecular models for vertebrate limb development. Cell 90, 979–990 (1997).

    Article  CAS  Google Scholar 

  10. Kelley, R. O. & Fallon, J. F. Ultrastructural analysis of the apical ectodermal ridge during vertebrate limb morphogenesis. I. The human forelimb with special reference to gap junctions. Dev. Biol. 51, 241–256 (1976).

    Article  CAS  Google Scholar 

  11. Francis-West, P., Ladher, R., Barlow, A. & Graveson, A. Signalling interactions during facial development. Mech. Dev. 75, 3–28 (1998).

    Article  CAS  Google Scholar 

  12. Crossley, P. H., Minowada, G., MacArthur, C. A. & Martin, G. R. Roles for FGF-8 in the induction, initiation, and maintenance of chick limb development. Cell 84, 127–136 (1996).

    Article  CAS  Google Scholar 

  13. Vogel, A., Rodriguez, C. & Izpisua-Belamonte, J. C. Involvement of FGF-8 in initiation, outgrowth, and patterning of the vertebrate limb. Development 122, 1737–1750 (1996).

    CAS  PubMed  Google Scholar 

  14. Loomis, C. A., Kimmel, R. A., Tong, C. X., Michaud, J. & Joyner, A. L. Analysis of the genetic pathway leading to formation of ectopic apical ectodermal ridges in mouse Engrailed-1 mutant limbs. Development 125, 1137–1148 (1998).

    CAS  PubMed  Google Scholar 

  15. Roberts, B., Lyons, G., Simandl, B. K., Kuroiwa, A. & Buckingham, M. The apical ectodermal ridge regulates Hox-7 and Hox-8 gene expression in developing chick limb buds. Genes Dev. 5, 2362–2374 (1991).

    Google Scholar 

  16. Wang, Y. & Sassoon, D. Ectoderm–mesenchyme and mesenchyme–mesenchyme interactions regulate Msx-1 expression and cellular differentiation in the murine limb bud. Dev. Biol. 168, 374–382 (1995).

    Article  CAS  Google Scholar 

  17. Chen, H. et al. Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nature Genet. 19, 51–55 (1998).

    Article  Google Scholar 

  18. Riddle, R. D. et al. Induction of the LIM homeobox gene Lmx1 by WNT7a establishes dorsoventral pattern in the vertebrate limb. Cell 83, 631–640 (1995).

    Article  CAS  Google Scholar 

  19. Parr, B. A. & McMahon, A. P. Dorsalizing signal Wnt-7a required for normal polarity of D–V and A–P axes of mouse limb. Nature 374, 350–353 (1995).

    Article  ADS  CAS  Google Scholar 

  20. Pellegrini, G. et al. Location and clonal analysis of stem cells and their differentiated progeny in the human occular surface. J. Cell Biol.(in the press).

  21. Byrne, C., Tainsky, M. & Fuchs, E. Programming gene expression in developing epidermis. Development 120, 2369–2383 (1994).

    CAS  PubMed  Google Scholar 

  22. Rheinwald, J. G. & Green, H. Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells. Cell 6, 331–344 (1975).

    Article  CAS  Google Scholar 

  23. Barrandon, Y. & Green, H. Three clonal types of keratinocytes with different capacities for multiplication. Proc. Natl Acad. Sci. USA 84, 2302–2306 (1987).

    Article  ADS  CAS  Google Scholar 

  24. Barrandon, Y. The epidermal stem cell: an overview. Dev. Biol. 4, 209–215 (1993).

    Article  CAS  Google Scholar 

  25. Watt, F. M. Epidermal stem cells: markers, patterning and the control of stem cell fate. Phil. Trans. R. Soc. Lond. B 358, 553–560 (1991).

    Google Scholar 

  26. Greer, J. & Roop, D. Loricrin, a major keratinocyte envelope protein, is expressed late in development. J. Invest. Term. 96, 553–560 (1991).

    Google Scholar 

  27. Calautti, E., Missero, C., Stein, P. L., Ezzell, R. M. & Dotto, G. P. Fyn tyrosine kinase is involved in keratinocyte differentiation control. Genes Dev. 9, 2279–2291 (1995).

    Article  CAS  Google Scholar 

  28. Jan, Y. N. & Jan, L. Y. Asymmetric cell division. Nature 392, 775–778 (1998).

    Article  ADS  CAS  Google Scholar 

  29. Donehower, L. A. et al. Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours. Nature 356, 215–221 (1992).

    Article  ADS  CAS  Google Scholar 

  30. Jacks, T. et al. Tumor spectrum analysis in p53 mutant mice. Curr. Biol. 4, 1–7 (1994).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank H. Green, M. Kirschner, P. Dotto, B. Olsen, N. Fukai, T. Rapoport, B.Quade, J. Glickman, P. Ferrara and T. Bestor for their support and for discussion; H. Green, G. Martin, A. McMahon, R. Johnson, A. Joyner and P. Dotto for reagents; L. Du for blastocyst injections; H. Liu for the 129 mouse genomic library; and J. Williams for histology preparations. This work was supported by grants from the NIH to R.B., C.T., A.S. and F.M.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Frank McKeon.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yang, A., Schweitzer, R., Sun, D. et al. p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature 398, 714–718 (1999). https://doi.org/10.1038/19539

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/19539

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