Dilated cardiomyopathy in transgenic mice expressing a mutant A subunit of protein phosphatase 2A

Journal Article

The protein phosphatase 2A (PP2A) holoenzyme consists of a catalytic subunit, C, and two regulatory subunits, A and B. The PP2A core enzyme is composed of subunits A and C. Both the holoenzyme and the core enzyme are similarly abundant in heart tissue. Transgenic mice were generated expressing high levels of a dominant negative mutant of the A subunit (AΔ5) in the heart, skeletal muscle, and smooth muscle that competes with the endogenous A subunit for binding the C subunit but does not bind B subunits. We found that the ratio of core enzyme to holoenzyme was increased in AΔ5-expressing hearts. Importantly, already at day I after birth, AΔ5-transgenic mice had an increased heart weight-to-body weight ratio that persisted throughout life. Echocardiographic analysis of AΔ5-transgenic hearts revealed increased end-diastolic and end-systolic dimensions and decreased fractional shortening. In addition, the thickness of the septum and of the left ventricular posterior wall was significantly reduced. On the basis of these findings, we consider the heart phenotype of AΔ5-transgenic mice to be a form of dilated cardiomyopathy that frequently leads to premature death.

Duke Authors

Cited Authors

  • Brewis, N; Ohst, K; Fields, K; Rapacciuolo, A; Chou, D; Bloor, C; Dillmann, W; Rockman, H; Walter, G

Published Date

  • 2000

Published In

Volume / Issue

  • 279 / 3 48-3

Start / End Page

  • H1307 - H1318

International Standard Serial Number (ISSN)

  • 0363-6135