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Managing the complexity of communication: regulation of gap junctions by post-translational modification

Journal

FRONTIERS IN PHARMACOLOGY
Volume 4, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2013.00130

Keywords

connexin; post translational modification; phosphorylation; sumoylation; nitrosylation; methylation; acetylation; ubiquitination

Funding

  1. Danish National Research Foundation
  2. Novo-Nordisk Foundation
  3. A. P. Moller Foundation for the Advancement of Medical Science
  4. Danish Council for Independent Research

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Gap junctions are comprised of connexins that form cell-to-cell channels which couple neighboring cells to accommodate the exchange of information. The need for communication does, however, change over time and therefore must be tightly controlled. Although the regulation of connexin protein expression by transcription and translation is of great importance, the trafficking, channel activity and degradation are also under tight control. The function of connexins can be regulated by several post translational modifications, which affect numerous parameters; including number of channels, open probability, single channel conductance or selectivity. The most extensively investigated post translational modifications are phosphorylations, which have been documented in all mammalian connexins. Besides phosphorylations, some connexins are known to be ubiquitinated, SUMOylated, nitrosylated, hydroxylated, acetylated, methylated, and y-carboxyglutamated. The aim of the present review is to summarize our current knowledge of post translational regulation of the connexin family of proteins.

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