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Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3

Nature Genetics volume 18, pages 283–286 (1998)Cite this article

Abstract

Waardenburg syndrome (WS) is a hereditary disorder that causes hypopigmentation and hearing impairment. Depending on additional symptoms, WS is classified into four types1: WS1, WS2, WS3 and WS4. Mutations in MITF (mi crophthalmia-associated t ranscription f actor) and PAX3, encoding transcription factors, are responsible for WS2 and WS1/WS3, respectively1. We have previously shown that MITF transactivates the gene for tyrosinase, a key enzyme for melanogenesis, and is critically involved in melanocyte differentiation2. Absence of melanocytes affects pigmentation in the skin, hair and eyes, and hearing function in the cochlea3. Therefore, hypopigmentation and hearing loss in WS2 are likely to be the results of an anomaly of melanocyte differentiation caused by MITF mutations4,5. However, the molecular mechanism by which PAX3 mutations cause the auditory-pigmentary symptoms in WS1/WS3 remains to be explained. Here we show that PAX3, a transcription factor with a paired domain and a homeodomain, transactivates the MITF promoter. We further show that PAX3 proteins associated with WS1 in either the paired domain or the homeodomain fail to recognize and transactivate the MITF promoter. These results provide evidence that PAX3 directly regulates MITF, and suggest that the failure of this regulation due to PAX3 mutations causes the auditory-pigmentary symptoms in at least some individuals with WS1.

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References

  1. Read, A.P. & Newton, V.E. Waardenburg syndrome. J. Med. Genet. 34, 656–665 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Tachibana, M. et al. Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics. Nature Genet. 14, 50–54 (1996).

    Article  CAS  PubMed  Google Scholar 

  3. Tachibana, M. et al. Cochlear disorder associated with melanocyte anomaly in mice with a transgenic insertional mutation. Mol. Cell. Neurosci. 3, 433–445 (1992).

    Article  CAS  PubMed  Google Scholar 

  4. Tassabehji, M., Newton, V.E. & Read, A.P. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. Nature Genet. 8, 251–255 (1994).

    Article  CAS  PubMed  Google Scholar 

  5. Nobukuni, Y., Watanabe, A., Takeda, K., Skarka, H. & Tachibana, M. Analyses of loss-of-function mutations of the MITF gene suggest that haploinsufficiency is a cause of Waardenburg syndrome type 2A. Am. J. Hum. Genet. 59, 76–83 (1996).

    CAS  PubMed  PubMed Central  Google Scholar 

  6. Latchman, D.S. Transcription-factor mutations and disease. N. Engl. J. Med. 334, 28–33 (1996).

    Article  CAS  PubMed  Google Scholar 

  7. Semenza, G.L. Transcriptional regulation of gene expression: mechanisms and pathophysiology. Hum. Mutat. 3, 180–199 (1994).

    Article  CAS  PubMed  Google Scholar 

  8. Tassabehji, M. et al. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 355, 635–636 (1992).

    Article  CAS  PubMed  Google Scholar 

  9. Baldwin, C.T., Hoth, C.F., Amos, J.A., da-Silva, E.O. & Milunsky, A. An exonic mutation in the Hup2 paired domain gene causes Waardenburg's syndrome. Nature 355, 637–638 (1992).

    Article  CAS  PubMed  Google Scholar 

  10. Hoth, C.F. et al. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I). Am. J. Hum. Genet. 52, 455–462 (1993).

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Lalwani, A.K. et al. Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type I in two families. Am. J. Hum. Genet. 56, 75–83 (1995).

    CAS  PubMed  PubMed Central  Google Scholar 

  12. Tassabehji, M. et al. The mutational spectrum in Waardenburg syndrome. Hum. Mol. Genet. 4, 2131–2137 (1995).

    Article  CAS  PubMed  Google Scholar 

  13. Chalepakis, G., Goulding, M., Read, A., Strachan, T. & Gruss, P. Molecular basis of splotch and Waardenburg syndrome Pax-3 mutations. Proc. Natl. Acad. Sci. USA 91, 3685–3689 (1994).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Epstein, J.A., Shapiro, D.N., Chen, J., Lam, P.Y.P. & Maas, R.L. Pax3 modulates expression of the c-Met receptor during limb muscle development. Proc. Natl. Acad. Sci. USA 93, 4213–4218 (1996).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Opdecamp, K. et al. Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor. Development 124, 2377–2386 (1997).

    CAS  PubMed  Google Scholar 

  16. Fuse, N., Yasumoto, K., Suzuki, H., Takahashi, K. & Shibahara, S. Identification of a melanocyte-type promoter of the microphthalmia-associated transcription factor gene. Biochem. Biophys. Res. Comm. 219, 702–707 (1996).

    Article  CAS  PubMed  Google Scholar 

  17. Chalepakis, G., Wijnholds, J. & Gruss, P. Pax-3-DNA interaction: flexibility in the DNA binding and induction of DNA conformational changes by paired domains. Nucleic Acids Res. 22, 3131–3137 (1994).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Guazzi, S. et al. The thyroid transcription factor-1 gene is a candidate target for regulation by Hox proteins. EMBO J. 13, 3339–3347 (1994).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Macina, R.A., Barr, F.G., Galili, N. & Riethman, H.C. Genomic organization of the human PAX3 gene: DNA sequence analysis of the region disrupted in alveolar rhabdomyosarcoma. Genomics 26, 1–8 (1995).

    Article  CAS  PubMed  Google Scholar 

  20. Schreiber, E., Matthias, P., Müller, M.M. & Schaffner, W. Rapid detection of octamer binding proteins with ‘mini-extracts’, prepared from a small number of cells. Nucleic Acids Res. 17, 6419 (1989).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Fredericks,W.J. et al. The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3. Mol. Cell. Biol. 15, 1522–1535 (1995).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Jones, D.H. & Howard, B.H. A rapid method for the site-specific mutagenesis and directional subcloning by using the polymerase chain reaction to generate recombinant circles. BioTechniques 8, 178–183 (1990).

    CAS  PubMed  Google Scholar 

  23. Kamachi, Y. & Kondoh, H. Overlapping positive and negative regulatory elements determine lens-specific activity of the δ1-crystallin enhancer. Mol. Cell. Biol. 13, 5206–5215 (1993).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Miki, T. et al. Development of a highly efficient expression cDNA cloning system: application to oncogene isolation. Proc. Natl. Acad. Sci. USA 88, 5167–5171 (1991).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Sublett, J.E., Jeon, I.-S. & Shapiro, D.N. The alveolar rhabdomyosarcoma PAX3/FKHR fusion protein is a transcriptional activator. Oncogene 11, 545–552 (1995).

    CAS  PubMed  Google Scholar 

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Author notes

  1. Atsushi Watanabe

    Present address: Department of Biochemistry and Molecular Biology, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo, 113-8602, Japan

  2. Kazuhisa Takeda

    Present address: Department of Molecular Biology and Applied Physiology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Sendai, 980-8575, Japan

Authors and Affiliations

  1. Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rm 2A31, Rockville, Maryland, 20850, USA

    Atsushi Watanabe, Kazuhisa Takeda, Barbara Ploplis & Masayoshi Tachibana

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  1. Atsushi Watanabe
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  2. Kazuhisa Takeda
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  3. Barbara Ploplis
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  4. Masayoshi Tachibana
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Corresponding author

Correspondence to Masayoshi Tachibana.

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Watanabe, A., Takeda, K., Ploplis, B. et al. Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3. Nat Genet 18, 283–286 (1998). https://doi.org/10.1038/ng0398-283

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