PICK1 binds to calcineurin B and modulates the NFAT activity in PC12 cells.

In the central nervous system, calcineurin has been implicated in a number of Ca2+-sensitive pathways, including the regulation of neurotransmitter release and modulation of synaptic plasticity. PDZ domain-containing proteins also play an important role in the targeting and clustering of synaptic proteins. Using a yeast two-hybrid screen, we herein identified ...
the PDZ domain-containing protein PICK1 as a specific interactor of calcineurin B. The interaction of calcineurin B and PICK1 was confirmed by GST pull-down assay in HEK293 cells and immunoprecipitation using rat brain lysate. Calcineurin B contains the consensus C-terminal peptide sequence required for interacting with the PDZ domain. The deletion of this sequence was sufficient to abolish the interaction between calcineurin B and PICK1. In addition, the knockdown of PICK1 by RNA interference inhibited the calcineurin-dependent activation of NFAT in PC12 cells. These results suggest that PICK1 may be a positive regulator of calcineurin in the central nervous system.
Mesh Terms:
Animals, Brain, Calcineurin, Carrier Proteins, Humans, Immunoprecipitation, NFATC Transcription Factors, Nuclear Proteins, PC12 Cells, PDZ Domains, Rats, Two-Hybrid System Techniques
Biochem. Biophys. Res. Commun.
Date: Oct. 31, 2008
Download Curated Data For This Publication
80443
Switch View:
  • Interactions 3