The SH3 domain of the tight junction protein ZO-1 binds to a serine protein kinase that phosphorylates a region C-terminal to this domain

FEBS Lett. 1996 Dec 16;399(3):326-32. doi: 10.1016/s0014-5793(96)01352-x.

Abstract

ZO-1 is a tight junction phosphoprotein partially homologous to a tumor suppressor in Drosophila. The homologous region contains an SH3 domain with an unidentified function. Using fusion proteins containing the SH3 domain and various N- and C-terminal sequences, we tested for association of a kinase with this protein domain in extracts of MDCK cells. We show that the SH3 domain of ZO-1 binds a serine protein kinase that phosphorylates a region immediately C-terminal to the SH3 domain. This kinase associates specifically with the SH3 domain of ZO-1 and appears to be also associated with junctional complexes extracted from MDCK cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Dogs
  • Glutathione Transferase / metabolism
  • Membrane Proteins / metabolism*
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Precipitin Tests
  • Protein Binding
  • Protein Kinases / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Zonula Occludens-1 Protein
  • src Homology Domains

Substances

  • Membrane Proteins
  • Phosphoproteins
  • Recombinant Fusion Proteins
  • Zonula Occludens-1 Protein
  • Glutathione Transferase
  • Protein Kinases