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Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients - Nature

  • ️Downward, Julian
  • ️Thu Apr 23 1992
  • Letter
  • Published: 23 April 1992

Nature volume 356pages 713–715 (1992)Cite this article

Abstract

DEFECTS in the NF1 gene have been implicated in the inherited disorder neurofibromatosis type 1, which is characterized by several developmental abnormalities including an increased frequency of benign and malignant tumours of neural crest origin (neuro-fibromas and neurofibrosarcomas respectively)1. The NF1 gene encodes a ubiquitous protein homologous to p!20GAP, the GTPase-activating protein (GAP) for the products of the ras proto-oncogenes2–6. When expressed in non-mammalian systems, the region of the NF1 gene homologous to p!20GAP produces a protein with GAP-like activity7–9. Here we present evidence that the ras proteins in malignant tumour cell lines from patients with type 1 neurofibromatosis are in a constitutively activated state, as judged by the guanine nucleotide bound to them, and are necessary for cellular proliferation. These cells contain P21rasand p120GAP that are both functionally wild type, but barely any functional NF1 protein. Our results show that the NF1 protein is normally essential for correct negative regulation of ras proteins in the cell, even in the presence of normal p120GAP, and they support the hypothesis that NF1 is a tumour-suppressor gene whose product acts upstream of ras.

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References

  1. Riccardi, V. & Eichner, J. Neurofibromatosis: Phenotype, Natural History and Pathogenesis (Johns Hopkins Univ. Press, Baltimore, 1986).

    Google Scholar 

  2. Viskochil, D. et al. Cell 62, 187–192 (1990).

    Article  CAS  Google Scholar 

  3. Cawthorn, R. M. et al. Cell 62, 193–201 (1990).

    Article  Google Scholar 

  4. Wallace, M. R. et al. Science 249, 181–186 (1990).

    Article  ADS  CAS  Google Scholar 

  5. Xu, G. et al. Cell 62, 599–608 (1990).

    Article  CAS  Google Scholar 

  6. Buchberg, A. M., Cleveland, L. S., Jenkins, N. A. & Copeland, N. G. Nature 347, 291–294 (1990).

    Article  ADS  CAS  Google Scholar 

  7. Xu, G. et al. Cell 63, 835–841 (1990).

    Article  CAS  Google Scholar 

  8. Martin, G. A. et al. Cell 63, 843–849 (1990).

    Article  CAS  Google Scholar 

  9. Ballester, R. et al. Cell 63, 851–859 (1990).

    Article  CAS  Google Scholar 

  10. Downward, J. Curr. Opin. dev. Genet. 2, 13–18 (1992).

    Article  CAS  Google Scholar 

  11. Downward, J., Graves, J. D., Warne, P. H., Rayter, S. & Cantrell, D. A. Nature 346, 719–723 (1990).

    Article  ADS  CAS  Google Scholar 

  12. Hattori, S. et al. Biochem. biophys. Res. Commun. 177, 83–89 (1991).

    Article  CAS  Google Scholar 

  13. Gutmann, D. H., Wood, D. L. & Collins, F. S. Proc. natn. Acad. Sci. U.S.A. 88, 9658–9662 (1991).

    Article  ADS  CAS  Google Scholar 

  14. Fletcher, J. A. et al. New Engl. J. Med. 324, 436–443 (1991).

    Article  CAS  Google Scholar 

  15. Glover, T. W. et al. Genes, Chromosomes Cancer 3, 62–70 (1991).

    Article  CAS  Google Scholar 

  16. Nigro, J. M. et al. Nature 342, 705–708 (1989).

    Article  ADS  CAS  Google Scholar 

  17. Ridley, A. J., Paterson, H. F., Noble, M. & Land, H. EMBO J. 7, 1635–1645 (1988).

    Article  CAS  Google Scholar 

  18. Menon, A. G. et al. Proc. natn. Acad. Sci. U.S.A. 87, 5435–5439 (1990).

    Article  ADS  CAS  Google Scholar 

  19. Downward, J., de Gunzburg, J., Riehl, R. & Weinberg, R. A. Proc. natn. Acad. Sci. U.S.A. 85, 5774–5778 (1988).

    Article  ADS  CAS  Google Scholar 

  20. Cantrell, D. A., Collins, M. K. & Crumpton, M. J. Immunology 65, 343–349 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  21. Harlow, E. & Lane, D. Antibodies: a Laboratory Manual (Cold Spring Harbor Laboratory, New York, 1988).

    Google Scholar 

  22. Smith, M. R., DeGudicubus, S. J. & Stacey, D. W. Nature 320, 540–543 (1986).

    Article  ADS  CAS  Google Scholar 

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Author information

Author notes

  1. Julian Downward: To whom correspondence should be addressed

Authors and Affiliations

  1. Signal Transduction Laboratory, Imperial Cancer Research Fund, Lincoln's Inn Fields, London, WC2A 3PX, UK

    Tanya N. Basu & Julian Downward

  2. Howard Hughes Medical Institute and Departments of Internal Medicine and Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA

    David H. Gutmann & Francis S. Collins

  3. Department of Pathology, Brigham and Women's Hospital, 75 Francis Street, Boston, Massachusetts, 02115, USA

    Jonathan A. Fletcher

  4. Departments of Pediatrics and Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA

    Thomas W. Glover

Authors

  1. Tanya N. Basu

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  2. David H. Gutmann

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  3. Jonathan A. Fletcher

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  4. Thomas W. Glover

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  5. Francis S. Collins

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  6. Julian Downward

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Basu, T., Gutmann, D., Fletcher, J. et al. Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients. Nature 356, 713–715 (1992). https://doi.org/10.1038/356713a0

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  • Received: 10 January 1992

  • Accepted: 06 March 1992

  • Issue Date: 23 April 1992

  • DOI: https://doi.org/10.1038/356713a0