Molecular remodelling in hypertrophied hearts from polyomavirus large T-antigen transgenic mice

Mol Cell Biochem. 1995 Nov 22;152(2):131-41. doi: 10.1007/BF01076075.

Abstract

Polyomavirus large T-antigen transgenic mice develop cardiac hypertrophy characterized by an increase in atrial natriuretic factor and beta-myosin heavy chain isoform expression. The aim of this study was to examine changes in proto-oncogene expression in hypertrophied hearts from the transgenic mice. Expression of early growth response-1 (Egr-1) mRNA was detected in hearts from all 15 transgenic mice, but was not detectable in 13 control mice. Reverse transcriptase-polymerase chain reaction experiments using Egr-1-specific primers confirmed the increase in Egr-1 mRNA in enlarged hearts from the transgenic mice. Expression of c-jun, junD and Ha-ras mRNAs was increased in the transgenic hearts 3, 17 and 2.8-fold respectively. Western blots showed an increase in c-myc, c-jun and ras protein in hypertrophied transgenic hearts. Immunofluorescence analyses confirmed an increase in Egr-1 and c-jun protein in transgenic cardiomyocytes. Proliferating cell nuclear antigen, Ki-ras and HSP 90 mRNAs were decreased 22, 2.7 and 3-fold, respectively in the transgenic hearts. Not altered in most hypertrophied hearts was expression of c-fos, junB, p53, c-neu, c-myc, HSP70, HSP27, TGF-beta or IGF 1 mRNAs. Proto-oncogene and growth factor gene expression in hypertrophy induced by PVLT expression is modulated with some proto-oncogenes increased and others decreased in expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Polyomavirus Transforming / genetics*
  • Base Sequence
  • Cardiomegaly / genetics
  • Cardiomegaly / immunology
  • Cardiomegaly / physiopathology*
  • Gene Expression Regulation, Developmental / physiology*
  • Growth Substances / biosynthesis*
  • Metallothionein / genetics
  • Mice
  • Mice, Transgenic
  • Molecular Sequence Data
  • Promoter Regions, Genetic
  • Proto-Oncogene Proteins c-jun / biosynthesis
  • Proto-Oncogene Proteins c-myc / biosynthesis
  • Proto-Oncogenes
  • Stress, Physiological / genetics
  • Transcriptional Activation*
  • ras Proteins / biosynthesis

Substances

  • Antigens, Polyomavirus Transforming
  • Growth Substances
  • Proto-Oncogene Proteins c-jun
  • Proto-Oncogene Proteins c-myc
  • Metallothionein
  • ras Proteins