Metabolic activation of CaMKII by coenzyme A

Mol Cell. 2013 Nov 7;52(3):325-39. doi: 10.1016/j.molcel.2013.08.043. Epub 2013 Oct 3.

Abstract

Active metabolism regulates oocyte cell death via calcium/calmodulin-dependent protein kinase II (CaMKII)-mediated phosphorylation of caspase-2, but the link between metabolic activity and CaMKII is poorly understood. Here we identify coenzyme A (CoA) as the key metabolic signal that inhibits Xenopus laevis oocyte apoptosis by directly activating CaMKII. We found that CoA directly binds to the CaMKII regulatory domain in the absence of Ca(2+) to activate CaMKII in a calmodulin-dependent manner. Furthermore, we show that CoA inhibits apoptosis not only in X. laevis oocytes but also in Murine oocytes. These findings uncover a direct mechanism of CaMKII regulation by metabolism and further highlight the importance of metabolism in preserving oocyte viability.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / genetics
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism*
  • Caspase 2 / metabolism
  • Cell Survival / genetics
  • Coenzyme A / metabolism*
  • Gene Expression Regulation, Developmental
  • Mice
  • Oocytes / growth & development
  • Oocytes / metabolism*
  • Phosphorylation / genetics
  • Protein Binding
  • Signal Transduction
  • Transcriptional Activation
  • Xenopus laevis / growth & development
  • Xenopus laevis / metabolism*

Substances

  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Caspase 2
  • Coenzyme A