AI Article Synopsis

  • NrCAM is a member of the L1 family of cell adhesion molecules crucial for the nervous system's development and function, but its interactions with intracellular signaling pathways are not fully understood.
  • Through screening a rat brain cDNA library, SAP102 was identified as a new binding partner for NrCAM, confirmed by multiple biochemical and immunocytochemical methods.
  • The interaction is specific to NrCAM and dependent on its last three amino acids, with altered NrCAM constructs negatively affecting neurite extension in cerebellar granule cells, suggesting a larger signaling complex involvement.

Article Abstract

Neurone glial-related cell adhesion molecule (NrCAM) is a member of the L1 family of transmembrane cell adhesion receptors which are involved in the development and function of the mammalian nervous system. How these receptors interact with intracellular signalling pathways is not understood. To date the only identified binding partner to the cytoplasmic terminus of NrCAM is ankyrin G. We screened a developing rat brain cDNA yeast two-hybrid library with the cytoplasmic domain of NrCAM to identify further intracellular binding partners. We identified synapse associated protein 102 (SAP102) as a new binding partner for NrCAM. The interaction was confirmed biochemically using glutathione S-transferase (GST)-pull-down and tandem affinity purification, and also immunocytochemically as NrCAM and SAP102 co-localized in COS-7 and cerebellar granule cells. Binding was specific to NrCAM as neither neurofascin nor L1 bound SAP102, and this interaction was reliant on the last three amino acids of NrCAM. Additionally, NrCAM constructs whose last three amino acids had been deleted appeared to have a dominant negative effect on neurite extension of cerebellar granule cells. This is the first interaction reported for NrCAM, and its association with SAP102 suggests that it is part of a larger complex which can interact with many different signalling pathways.

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http://dx.doi.org/10.1111/j.1471-4159.2005.03271.xDOI Listing

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