PUBLICATION

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

Authors
Luxan, G., Casanova, J.C., Martinez-Poveda, B., Prados, B., D'Amato, G., Macgrogan, D., Gonzalez-Rajal, A., Dobarro, D., Torroja, C., Martinez, F., Izquierdo-García, J.L., Fernandez-Friera, L., Sabater-Molina, M., Kong, Y.Y., Pizarro, G., Ibañez, B., Medrano, C., García-Pavía, P., Gimeno, J.R., Monserrat, L., Jimenez-Borreguero, L.J., and de la Pompa, J.L.
ID
ZDB-PUB-130124-17
Date
2013
Source
Nature medicine   19(2): 193-201 (Journal)
Registered Authors
de la Pompa, José Luis, Macgrogan, Donal, Prados Pinto, Belen, Torroja, Carlos
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Cardiomyopathies/etiology*
  • Cardiomyopathies/genetics
  • Female
  • HEK293 Cells
  • Heart/embryology
  • Heart Ventricles*/embryology
  • Humans
  • Male
  • Mice
  • Molecular Sequence Data
  • Mutation*
  • Protein Multimerization
  • Receptors, Notch/physiology*
  • Signal Transduction/physiology*
  • Ubiquitin-Protein Ligases/genetics*
  • Ubiquitin-Protein Ligases/physiology
  • Zebrafish
PubMed
23314057 Full text @ Nat. Med.
Abstract

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.

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Mutations / Transgenics
Human Disease / Model
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