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:

Bad bones, grey hair, one mutation

Osteopetrosis, a disease characterized by dense bones, is now pinned to the same gene that underlies a coat-color defect in mice (pages 399–406).

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: Strange relationship? Chalhoub et al. identified a mutation in mice that affects both melanocytes and osteoclasts, and may cause osteopetrosis in humans.

References

  1. Chalhoub, N. et al. Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human. Nat. Med. 9, 399–406 (2003).

    Article  CAS  Google Scholar 

  2. Karsenty, G. & Wagner, E.F. Reaching a genetic and molecular understanding of skeletal development. Dev. Cell 2, 389–406 (2002).

    Article  CAS  Google Scholar 

  3. Vaananen, K. & Zhao, H. Osteoclast function: biology and mechanisms. in Principles of Bone Biology (eds. Bilezikian, J.P., Raisz, L.G. & Rodan, G.A.) 127–139 (Academic Press, San Diego, California, 2002).

    Google Scholar 

  4. Seiberg, M. Keratinocyte-melanocyte interactions during melanosome transfer. Pigment Cell Res. 14, 236–242 (2001).

    Article  CAS  Google Scholar 

  5. Scott, G. Rac and Rho: the story behind melanocyte dendrite formation. Pigment Cell Res. 15, 322–330 (2002).

    Article  CAS  Google Scholar 

  6. Langford, G.M. Myosin-v, a versatile motor for short-range vesicle transport. Traffic 12, 859–865 (2002).

    Article  Google Scholar 

  7. Mansky, K.C., Sankar, U., Han, J. & Ostrowski, M.C. Microphthalmia transcription factor is a target of the p38 MAPK pathway in response to receptor activator of NF-κB ligand signaling. J. Biol. Chem. 277, 11077–11083 (2002).

    Article  CAS  Google Scholar 

  8. McGill, G.G. et al. Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability. Cell 109, 707–718 (2002).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Boyce, B. Bad bones, grey hair, one mutation. Nat Med 9, 395–396 (2003). https://doi.org/10.1038/nm0403-395

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/nm0403-395

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