Turnover and phosphorylation dynamics of connexin43 gap junction protein in cultured cardiac myocytes

Biochem J. 1991 Jan 1;273(Pt 1)(Pt 1):67-72. doi: 10.1042/bj2730067.


Cultured cardiomyocytes were used to study the turnover and post-translational modification of connexin43 (Cx43), a major gap junction protein in neonatal cardiac myocytes. Immunoprecipitation of [35S]Met-labelled lysates with anti-Cx43 antibodies followed by analysis using SDS/PAGE and fluorography revealed two bands, one at 40 kDa and the other at 42 kDa. Alkaline phosphatase treatment of [35S]Met-labelled Cx43 eliminated the band at 42 kDa, suggesting that it represented a phosphorylated form of the protein. This was confirmed by [32P]P1 incorporation into the 42 kDa band, but not into the band at 40 kDa. In addition, another alkaline phosphatase-sensitive phosphorylated form of Cx43 was identified at 44 kDa. In pulse-chase experiments, the half-life of Cx43 in cardiomyocytes was determined to be 1-2 h. Furthermore, the turnover rate of phosphate groups on Cx43 was found to be experimentally defined by the half-life of the protein. The observation that phosphate groups can remain with the protein throughout its life is consistent with the finding that in isolated adult rat heart gap junction plaques, Cx43 is primarily phosphorylated. We postulate that the rapid turnover of Cx43 and its multiple sites of phosphorylation play important roles in the regulation of cell-cell communication via gap junctions.

Publication types

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

MeSH terms

  • Alkaline Phosphatase
  • Animals
  • Cells, Cultured
  • Connexins
  • Electrophoresis, Polyacrylamide Gel
  • Hydrolysis
  • Intercellular Junctions / metabolism*
  • Membrane Proteins / metabolism*
  • Myocardium / cytology
  • Myocardium / metabolism*
  • Phosphorylation
  • Precipitin Tests
  • Rats
  • Substrate Specificity


  • Connexins
  • Membrane Proteins
  • Alkaline Phosphatase