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.

Regulation of Lethal giant larvae by Dishevelled

Abstract

The establishment of polarity in many cell types depends on Lgl, the tumour suppressor product of lethal giant larvae, which is involved in basolateral protein targeting1,2,3,4. The conserved complex of Par3, Par6 and atypical protein kinase C5,6,7,8 phosphorylates and inactivates Lgl at the apical surface; however, the signalling mechanisms that coordinate cell polarization in development are not well defined. Here we show that a vertebrate homologue of Lgl associates with Dishevelled, an essential mediator of Wnt signalling, and that Dishevelled regulates the localization of Lgl in Xenopus ectoderm and Drosophila follicular epithelium. We show that both Lgl and Dsh are required for normal apical–basal polarity of Xenopus ectodermal cells. In addition, we show that the Wnt receptor Frizzled 8, but not Frizzled 7, causes Lgl to dissociate from the cortex with the concomitant loss of its activity in vivo. These findings suggest a molecular basis for the regulation of cell polarity by Frizzled and Dishevelled.

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

Relevant articles

Open Access articles citing this article.

Access options

Buy article

Get time limited or full article access on ReadCube.

$32.00

All prices are NET prices.

Figure 1: Lgl1 modulates apical–basal polarity in superficial ectoderm.
Figure 2: Dsh is required for Lgl activity and membrane localization.
Figure 3: Lgl1 and Dsh are required for apical–basal polarity in embryonic ectoderm.
Figure 4: Fz8 alters localization and activity of Lgl.

References

  1. Wodarz, A. Establishing cell polarity in development. Nature Cell Biol. 4, E39–E44 (2002)

    CAS  Article  Google Scholar 

  2. Ohshiro, T., Yagami, T., Zhang, C. & Matsuzaki, F. Role of cortical tumour-suppressor proteins in asymmetric division of Drosophila neuroblast. Nature 408, 593–596 (2000)

    ADS  CAS  Article  Google Scholar 

  3. Bilder, D., Li, M. & Perrimon, N. Cooperative regulation of cell polarity and growth by Drosophila tumour suppressors. Science 289, 113–116 (2000)

    ADS  CAS  Article  Google Scholar 

  4. Musch, A. et al. Mammalian homolog of Drosophila tumour suppressor lethal (2) giant larvae interacts with basolateral exocytic machinery in Madin–Darby canine kidney cells. Mol. Biol. Cell 13, 158–168 (2002)

    CAS  Article  Google Scholar 

  5. Etienne-Manneville, S. & Hall, A. Cdc42 regulates GSK-3β and adenomatous polyposis coli to control cell polarity. Nature 421, 753–756 (2003)

    ADS  CAS  Article  Google Scholar 

  6. Benton, R. & St Johnston, D. Drosophila PAR-1 and 14–3-3 inhibit Bazooka/PAR-3 to establish complementary cortical domains in polarized cells. Cell 115, 691–704 (2003)

    CAS  Article  Google Scholar 

  7. Chia, W. & Yang, X. Asymmetric division of Drosophila neural progenitors. Curr. Opin. Genet. Dev. 12, 459–464 (2002)

    CAS  Article  Google Scholar 

  8. Ohno, S. Intercellular junctions and cellular polarity: the PAR–aPKC complex, a conserved core cassette playing fundamental roles in cell polarity. Curr. Opin. Cell Biol. 13, 641–648 (2001)

    CAS  Article  Google Scholar 

  9. Shi, S. H., Jan, L. Y. & Jan, Y. N. Hippocampal neuronal polarity specified by spatially localized mPar3/mPar6 and PI 3-kinase activity. Cell 112, 63–75 (2003)

    CAS  Article  Google Scholar 

  10. Nakaya, M. et al. Meiotic maturation induces animal-vegetal asymmetric distribution of aPKC and ASIP/PAR-3 in Xenopus oocytes. Development 127, 5021–5031 (2000)

    CAS  PubMed  Google Scholar 

  11. Doe, C. Q. & Bowerman, B. Asymmetric cell division: fly neuroblast meets worm zygote. Curr. Opin. Cell Biol. 13, 68–75 (2001)

    CAS  Article  Google Scholar 

  12. Plant, P. J. et al. A polarity complex of mPar-6 and atypical PKC binds, phosphorylates and regulates mammalian Lgl. Nature Cell Biol. 5, 301–308 (2003)

    CAS  Article  Google Scholar 

  13. Betschinger, J., Mechtler, K. & Knoblich, J. A. The Par complex directs asymmetric cell division by phosphorylating the cytoskeletal protein Lgl. Nature 422, 326–330 (2003)

    ADS  CAS  Article  Google Scholar 

  14. Yamanaka, T. et al. Mammalian Lgl forms a protein complex with PAR-6 and aPKC independently of PAR-3 to regulate epithelial cell polarity. Curr. Biol. 13, 734–743 (2003)

    CAS  Article  Google Scholar 

  15. Hutterer, A., Betschinger, J., Petronczki, M. & Knoblich, J. A. Sequential roles of Cdc42, Par-6, aPKC, and Lgl in the establishment of epithelial polarity during Drosophila embryogenesis. Dev. Cell 6, 845–854 (2004)

    CAS  Article  Google Scholar 

  16. Klezovitch, O., Fernandez, T. E., Tapscott, S. J. & Vasioukhin, V. Loss of cell polarity causes severe brain dysplasia in Lgl1 knockout mice. Genes Dev. 18, 559–571 (2004)

    CAS  Article  Google Scholar 

  17. Lehman, K., Rossi, G., Adamo, J. E. & Brennwald, P. Yeast homologues of tomosyn and lethal giant larvae function in exocytosis and are associated with the plasma membrane SNARE, Sec9. J. Cell Biol. 146, 125–140 (1999)

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Baas, A. F. et al. Complete polarization of single intestinal epithelial cells upon activation of LKB1 by STRAD. Cell 116, 457–466 (2004)

    CAS  Article  Google Scholar 

  19. Eaton, S. Cell biology of planar polarity transmission in the Drosophila wing. Mech. Dev. 120, 1257–1264 (2003)

    CAS  Article  Google Scholar 

  20. Mlodzik, M. Planar cell polarization: do the same mechanisms regulate Drosophila tissue polarity and vertebrate gastrulation? Trends Genet. 18, 564–571 (2002)

    CAS  Article  Google Scholar 

  21. Tada, M. & Smith, J. C. Xwnt11 is a target of Xenopus Brachyury: regulation of gastrulation movements via Dishevelled, but not through the canonical Wnt pathway. Development 127, 2227–2238 (2000)

    CAS  PubMed  Google Scholar 

  22. Wallingford, J. B. et al. Dishevelled controls cell polarity during Xenopus gastrulation. Nature 405, 81–85 (2000)

    ADS  CAS  Article  Google Scholar 

  23. Cadigan, K. M. & Nusse, R. Wnt signalling: a common theme in animal development. Genes Dev. 11, 3286–3305 (1997)

    CAS  Article  Google Scholar 

  24. Chalmers, A. D., Strauss, B. & Papalopulu, N. Oriented cell divisions asymmetrically segregate aPKC and generate cell fate diversity in the early Xenopus embryo. Development 130, 2657–2668 (2003)

    CAS  Article  Google Scholar 

  25. Chalmers, A. D. et al. Crumbs3 and Lgl2 control apicobasal polarity in early vertebrate development. Development 132, 977–986 (2005)

    CAS  Article  Google Scholar 

  26. Sheldahl, L. C. et al. Dishevelled activates Ca2+ flux, PKC, and CamKII in vertebrate embryos. J. Cell Biol. 161, 769–777 (2003)

    CAS  Article  Google Scholar 

  27. Xu, T. & Rubin, G. M. Analysis of genetic mosaics in developing and adult Drosophila tissues. Development 117, 1223–1237 (1993)

    CAS  PubMed  Google Scholar 

  28. Wu, J., Klein, T. J. & Mlodzik, M. Subcellular localization of frizzled receptors, mediated by their cytoplasmic tails, regulates signalling pathway specificity. PLoS Biol. 2, E158 (2004)

    Article  Google Scholar 

  29. Bellaiche, Y., Beaudoin-Massiani, O., Stuttem, I. & Schweisguth, F. The planar cell polarity protein Strabismus promotes Pins anterior localization during asymmetric division of sensory organ precursor cells in Drosophila. Development 131, 469–478 (2004)

    CAS  Article  Google Scholar 

  30. Brott, B. K. & Sokol, S. Y. A vertebrate homologue of the cell cycle regulator Dbf4 is a Wnt inhibitor required for heart development. Dev. Cell 8, 703–715 (2005)

    CAS  Article  Google Scholar 

Download references

Acknowledgements

We thank K. Itoh, J. Green, J. LeBlanc-Straceski, B. Lake and S. Dhawan for discussions and comments on the manuscript; J. Knoblich for anti-Lgl antibody; S. Citi for anti-occludin antibodies; A. Chalmers for the immunohistochemistry protocol; B. Brott for initial work on the yeast two-hybrid screen; and A. Djiane for help with the Drosophila studies. This work was supported by NIH grants (to S.Y.S. and M.M.) and an NIH training grant (to G.L.D.).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sergei Y. Sokol.

Ethics declarations

Competing interests

Reprints and permissions information is available at npg.nature.com/reprintsandpermissions. The authors declare no competing financial interests.

Supplementary information

Supplementary Figures

This file contains Supplementary Figures 1–3. Supplementary Figure 1 demonstrates specificity of anti-Lgl antibodies using western analysis of Xenopus embryo lysates. Supplementary Figure 2 shows Dsh and Lgl constructs used in this study, and immunoprecipitation experiments demonstrating Dsh and Lgl interactions in vivo. Supplementary Figure 3 shows specific depletion of Lgl1 protein in stage 10 embryos upon injection of LglMO. (DOC 467 kb)

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Dollar, G., Weber, U., Mlodzik, M. et al. Regulation of Lethal giant larvae by Dishevelled. Nature 437, 1376–1380 (2005). https://doi.org/10.1038/nature04116

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature04116

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