• Register
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.


Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.


Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy.

Left ventricular noncompaction (LVNC) causes prominent ventricular trabeculations and reduces cardiac systolic function. The clinical presentation of LVNC ranges from asymptomatic to heart failure. We show that germline mutations in human MIB1 (mindbomb homolog 1), which encodes an E3 ubiquitin ligase that promotes endocytosis of the NOTCH ligands DELTA and JAGGED, cause LVNC in autosomal-dominant pedigrees, with affected individuals showing reduced NOTCH1 activity and reduced expression of target genes. Functional studies in cells and zebrafish embryos and in silico modeling indicate that MIB1 functions as a dimer, which is disrupted by the human mutations. Targeted inactivation of Mib1 in mouse myocardium causes LVNC, a phenotype mimicked by inactivation of myocardial Jagged1 or endocardial Notch1. Myocardial Mib1 mutants show reduced ventricular Notch1 activity, expansion of compact myocardium to proliferative, immature trabeculae and abnormal expression of cardiac development and disease genes. These results implicate NOTCH signaling in LVNC and indicate that MIB1 mutations arrest chamber myocardium development, preventing trabecular maturation and compaction.

Pubmed ID: 23314057


  • Luxán G
  • Casanova JC
  • Martínez-Poveda B
  • Prados B
  • D'Amato G
  • MacGrogan D
  • Gonzalez-Rajal A
  • Dobarro D
  • Torroja C
  • Martinez F
  • Izquierdo-García JL
  • Fernández-Friera L
  • Sabater-Molina M
  • Kong YY
  • Pizarro G
  • Ibañez B
  • Medrano C
  • García-Pavía P
  • Gimeno JR
  • Monserrat L
  • Jiménez-Borreguero LJ
  • de la Pompa JL


Nature medicine

Publication Data

February 7, 2013

Associated Grants


Mesh Terms

  • Amino Acid Sequence
  • Animals
  • Cardiomyopathies
  • Female
  • HEK293 Cells
  • Heart
  • Heart Ventricles
  • Humans
  • Male
  • Mice
  • Molecular Sequence Data
  • Mutation
  • Protein Multimerization
  • Receptors, Notch
  • Signal Transduction
  • Ubiquitin-Protein Ligases
  • Zebrafish