Phosphoregulation of the titin-cap protein telethonin in cardiac myocytes

J Biol Chem. 2014 Jan 17;289(3):1282-93. doi: 10.1074/jbc.M113.479030. Epub 2013 Nov 26.

Abstract

Telethonin (also known as titin-cap or t-cap) is a muscle-specific protein whose mutation is associated with cardiac and skeletal myopathies through unknown mechanisms. Our previous work identified cardiac telethonin as an interaction partner for the protein kinase D catalytic domain. In this study, kinase assays used in conjunction with MS and site-directed mutagenesis confirmed telethonin as a substrate for protein kinase D and Ca(2+)/calmodulin-dependent kinase II in vitro and identified Ser-157 and Ser-161 as the phosphorylation sites. Phosphate affinity electrophoresis and MS revealed endogenous telethonin to exist in a constitutively bis-phosphorylated form in isolated adult rat ventricular myocytes and in mouse and rat ventricular myocardium. Following heterologous expression in myocytes by adenoviral gene transfer, wild-type telethonin became bis-phosphorylated, whereas S157A/S161A telethonin remained non-phosphorylated. Nevertheless, both proteins localized predominantly to the sarcomeric Z-disc, where they partially replaced endogenous telethonin. Such partial replacement with S157A/S161A telethonin disrupted transverse tubule organization and prolonged the time to peak of the intracellular Ca(2+) transient and increased its variance. These data reveal, for the first time, that cardiac telethonin is constitutively bis-phosphorylated and suggest that such phosphorylation is critical for normal telethonin function, which may include maintenance of transverse tubule organization and intracellular Ca(2+) transients.

Keywords: CaMKII; Cardiac Muscle; Cardiomyopathy; Excitation-Contraction Coupling; Protein Kinase D (PKD); Protein Phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Animals
  • Calcium / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / genetics
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism
  • Cells, Cultured
  • Connectin / genetics
  • Connectin / metabolism*
  • Heart Ventricles / cytology
  • Heart Ventricles / metabolism
  • Humans
  • Male
  • Mice
  • Microtubules / genetics
  • Microtubules / metabolism
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Mutation, Missense
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / metabolism*
  • Phosphorylation / physiology
  • Protein Kinase C / genetics
  • Protein Kinase C / metabolism
  • Rats
  • Rats, Wistar
  • Sarcomeres / genetics
  • Sarcomeres / metabolism

Substances

  • Connectin
  • Muscle Proteins
  • TCAP protein, human
  • Tcap protein, mouse
  • Tcap protein, rat
  • protein kinase D
  • Protein Kinase C
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium