PKA-dependent phosphorylation of cardiac myosin binding protein C in transgenic mice

Cardiovasc Res. 2001 Jul;51(1):80-8. doi: 10.1016/s0008-6363(01)00273-5.

Abstract

Objective: To investigate the physiological role of cAMP-dependent protein kinase A (PKA)-mediated, cardiac myosin binding protein C (MyBP-C) phosphorylation.

Methods: A cardiac MyBP-C cDNA lacking nine amino acids, which contained a phosphorylation site, was made, and subsequently used to generate multiple lines of transgenic mice. Upon confirming that a partial replacement of endogenous protein with transgenic protein occurred, the biochemical and physiological consequences were studied. PKA-dependent phosphorylation assays were used to estimate the phosphorylation states of major cardiac PKA substrates. Myofibril Mg-ATPase activities were also measured. Isolated working heart and whole animal exercise studies were used to measure the physiological changes.

Results: Transgenic mice displayed a compensatory response, with PKA-mediated phosphorylation of both troponin I and phospholamban showing significant increases. The remaining endogenous cardiac MyBP-C also showed increased phosphorylation levels. Maximal Mg(2+)-ATPase activity was increased. Significant functional changes at both the whole organ and whole animal levels also occurred. Parameters reflecting cardiac contractility and relaxation increased about 22 and 25%, respectively, in the mutant relative to wild type mice (n=5, P<0.001). In young adults the capacity for stress exercise, quantitated using an exercise treadmill regimen, was substantially enhanced (n=6, P<0.01).

Conclusions: Cardiac MyBP-C phosphorylation plays an important physiological role and that the protein's degree of phosphorylation is coordinated with the phosphorylation levels of other proteins within the contractile apparatus.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Western
  • Ca(2+) Mg(2+)-ATPase / metabolism
  • Carrier Proteins / analysis
  • Carrier Proteins / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / genetics
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Genetic Engineering
  • Mice
  • Mice, Transgenic
  • Myocardial Contraction / physiology*
  • Myocardium / chemistry
  • Myocardium / metabolism*
  • Myofibrils / enzymology
  • Perfusion
  • Phosphorylation
  • Signal Transduction / physiology*

Substances

  • Carrier Proteins
  • myosin-binding protein C
  • Cyclic AMP-Dependent Protein Kinases
  • Ca(2+) Mg(2+)-ATPase