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  • The interaction of mPar3 with the ubiquitin ligase Smurf2 is required for the establishment of neuronal polarity.

The interaction of mPar3 with the ubiquitin ligase Smurf2 is required for the establishment of neuronal polarity.

The Journal of biological chemistry (2007-10-02)
Jens C Schwamborn, Mohammad R Khazaei, Andreas W Püschel
ABSTRACT

The Par polarity complex consisting of the evolutionarily conserved proteins mPar3, mPar6, and aPKC regulates cell polarity in many cell types including neurons. Here we show that mPar3 is required for the establishment of neuronal polarity and links the Smurf2 to Kinesin-2. The HECT domain E3 ubiquitin ligase Smurf2 ensures that neurons extend only a single axon by initiating the degradation of inactive Rap1B through the ubiquitin/proteasome system. Its interaction with mPar3 is required to localize Smurf2 to growth cones and restrict Rap1B to the axon. Interfering with the binding of mPar3 to Kinesin-2 or Smurf2 to mPar3 and knockdown of mPar3 by RNAi disrupt the establishment of neuronal polarity through the failure to restrict Rap1B to a single neurite.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Anti-Partitioning-defective 3 Antibody, Upstate®, from rabbit
Sigma-Aldrich
Anti-Tau-1 Antibody, clone PC1C6, clone PC1C6, Chemicon®, from mouse
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Anti-Microtubule-Associated Protein 2 (MAP2) Antibody, Chemicon®, from rabbit
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Monoclonal Anti-α-Tubulin antibody produced in mouse, clone DM1A, ascites fluid