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Targeted disruption of hesr2 results in atrioventricular valve anomalies that lead to heart dysfunction.

Genes involved in the Notch signaling pathway have been shown to be critical regulators of cardiovascular development. In vitro studies have revealed that the Notch signaling pathway directly regulates transcription of hairy and enhancer of split-related (hesr) genes, encoding basic helix-loop-helix transcription factors. To assess the functional role of hesr genes in cardiovascular development, we generated mice with a targeted disruption of the hesr2 gene and used echocardiography to analyze heart function of the mutant mice. In the early postnatal period, a majority of hesr2 homozygous mice die as a result of congestive heart failure accompanied by pronounced heart enlargement. Transthoracic echocardiography on 5-day-old homozygous mice revealed tricuspid and mitral valve regurgitation and a dilated left ventricular chamber with markedly diminished fractional shortening of the left ventricle. The hemodynamic anomalies were accompanied by morphological changes, such as dysplastic atrioventricular (AV) valves, a perimembranous ventricular septal defect, and a secundum atrial septal defect. AV valve regurgitations attributable to dysplasia of the AV valves were most likely responsible for the heart dysfunction in hesr2 homozygous mice. These observations indicate that the Notch signaling target hesr2 plays an important role in the formation and function of the AV valves. In addition, hesr2 activity may be important for proper development of cardiomyocytes, thereby assuring normal left ventricular contractility. Because of the unique spectrum of cardiac anomalies expressed by hesr2-null mice, they represent a useful model system for elucidating the genetic basis of heart dysfunction.

Pubmed ID: 15297376

Authors

  • Kokubo H
  • Miyagawa-Tomita S
  • Tomimatsu H
  • Nakashima Y
  • Nakazawa M
  • Saga Y
  • Johnson RL

Journal

Circulation research

Publication Data

September 3, 2004

Associated Grants

None

Mesh Terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Eye Proteins
  • Gene Expression
  • Gene Targeting
  • Growth Disorders
  • Heart
  • Heart Defects, Congenital
  • Heart Failure
  • Mice
  • Mice, Knockout
  • Mitral Valve
  • Mitral Valve Insufficiency
  • Myocardium
  • Repressor Proteins
  • Tricuspid Valve
  • Tricuspid Valve Insufficiency
  • Ventricular Dysfunction, Left