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Ubiquitin ligase Smurf1 controls osteoblast activity and bone homeostasis by targeting MEKK2 for degradation.

Bone is constantly resorbed and formed throughout life by coordinated actions of osteoclasts and osteoblasts. Here we show that Smurf1, a HECT domain ubiquitin ligase, has a specific physiological role in suppressing the osteogenic activity of osteoblasts. Smurf1-deficient mice are born normal but exhibit an age-dependent increase of bone mass. The cause of this increase can be traced to enhanced activities of osteoblasts, which become sensitized to bone morphogenesis protein (BMP) in the absence of Smurf1. However, loss of Smurf1 does not affect the canonical Smad-mediated intracellular TGFbeta or BMP signaling; instead, it leads to accumulation of phosphorylated MEKK2 and activation of the downstream JNK signaling cascade. We demonstrate that Smurf1 physically interacts with MEKK2 and promotes the ubiquitination and turnover of MEKK2. These results indicate that Smurf1 negatively regulates osteoblast activity and response to BMP through controlling MEKK2 degradation.

Pubmed ID: 15820682

Authors

  • Yamashita M
  • Ying SX
  • Zhang GM
  • Li C
  • Cheng SY
  • Deng CX
  • Zhang YE

Journal

Cell

Publication Data

April 8, 2005

Associated Grants

  • Agency: NCI NIH HHS, Id: Z01 BC010419-08
  • Agency: NCI NIH HHS, Id: ZIA BC011168-01

Mesh Terms

  • Animals
  • Bone Density
  • Bone Morphogenetic Proteins
  • Bone and Bones
  • Cells, Cultured
  • JNK Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase Kinase 2
  • Mice
  • Mice, Knockout
  • Osteoblasts
  • Phosphorylation
  • Protein Binding
  • Signal Transduction
  • Transforming Growth Factor beta
  • Ubiquitin-Protein Ligases