Identification of two focal adhesion targeting sequences in the adapter molecule p130(Cas)

M T Harte, M Macklem, C L Weidow, J T Parsons, A H Bouton

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25 Citations (Scopus)


The adapter molecule CAS is localized primarily within focal adhesions in fibroblasts. Because many of the cellular functions attributed to CAS are likely to be dependent on its presence in focal adhesions, this study was undertaken to identify regions of the protein that are involved in its localization. The SH3 domain of CAS, when expressed in isolation from the rest of the protein, was able to target to focal adhesions, whereas a variant containing a point mutation that rendered the SH3 domain unable to associate with FAK remained cytoplasmic. However, in the context of full-length CAS, this mutation did not prevent CAS localization to focal adhesions. Two other variants of CAS that contained deletions of either the SH3 domain alone, or the SH3 domain together with an adjoining proline-rich region, also retained the capacity to localize to focal adhesions. A second focal adhesion targeting region was mapped to the extreme carboxy terminus of CAS. The identification of this second focal adhesion targeting domain in CAS ascribes a previously unknown function to the highly conserved C terminus of CAS. The regulated targeting of CAS to focal adhesions by two independent domains may reflect the important role of CAS within this subcellular compartment.
Original languageEnglish
Pages (from-to)34-48
Number of pages15
JournalBiochimica et biophysica acta
Issue number1-2
Publication statusPublished - 11 Dec 2000


  • Animals
  • Binding Sites
  • Cell Line
  • Crk-Associated Substrate Protein
  • Fluorescent Antibody Technique
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Focal Adhesions
  • Helix-Loop-Helix Motifs
  • Mutation
  • Phosphoproteins
  • Phosphorylation
  • Protein-Tyrosine Kinases
  • Proteins
  • Rats
  • Retinoblastoma-Like Protein p130
  • Transfection
  • src Homology Domains


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